Manager, Accounting (Revenue)

🏢 Summary: Newly created Revenue Accounting Manager role responsible for full ownership of revenue recognition processes, including partnership and commercial revenue, under ASC 606 in a life sciences environment. The position leads complex contract assessments, month‑end close activities, SOX-compliant controls, and revenue disclosures, while partnering cross‑functionally to ensure accurate financial reporting. This is a high-impact, in-office role requiring strong technical accounting expertise and experience in biotech or pharmaceutical settings. 🗂️ Requirements: Bachelor's degree in Accounting, Finance, or related field, 5+ years of financial accounting experience with strong focus on ASC 606 revenue recognition, In-depth knowledge of U.S. GAAP, Experience with SOX compliance requirements, Experience managing complex monthly and quarterly close processes, Ability to assess complex contracts and determine revenue recognition treatment, Experience preparing revenue-related disclosures (10-Q, 10-K), Authorization to work in the country of employment 📃 Skills: ASC606, GAAP, SOX, RevenueRecognition, FinancialReporting, JournalEntries, Reconciliations, OrderToCash, GrossToNet, SECReporting 🏢 Description: The Position Arrowhead is seeking a Revenue Accounting Manager to join its Finance & Accounting team at its Pasadena, CA headquarters. Reporting to the Senior Accounting Manager and working closely with the Controller, the Revenue Accounting Manager will manage all aspects of partnership/collaboration accounting and commercial revenue. This is a newly created, high-impact role designed to build and scale best-in-class revenue recognition processes in the life sciences industry, where revenue models are complex and highly specialized. The role carries full ownership of the company's revenue framework and serves as the subject-matter expert for ASC 606 revenue accounting. Success in this position requires a strong mix of technical accounting expertise, leadership, and cross-functional collaboration to ensure accurate financial reporting, operational efficiency, and SOX compliance. The ideal candidate is detail-driven, highly responsive, tech-savvy, and adaptable in a fast-moving environment, with 5+ years of progressive experience in finance or accounting, with a significant focus on revenue recognition (ASC 606), preferably within biotech or pharmaceutical companies. This role is based in Pasadena or San Diego, CA with an expectation to be in office 5 days a week. Responsibilities Develop a deep understanding of partnership and customer contracts and serve as the subject-matter expert on revenue accounting under ASC 606 and U.S. GAAP. Review and assess complex contracts, including partnership arrangements, to determine appropriate revenue recognition treatment and disclosure requirements. Establish and maintain revenue accounting policies and procedures in accordance with regulatory standards and SOX control requirements. Partner with FP&A to lead cross-functional efforts to ensure accurate tracking of actual labor hours and facilitate updates to budgeted resource assumptions. Ensure inputs to input-method revenue recognition are well-supported, accurate, and audit-ready. Perform order-to-cash month-end and quarter-end close activities, including the preparation and posting of journal entries, completion of balance sheet reconciliations and flux analysis. Assist with gross-to-net revenue accounting, including reviewing support provided by third parties and month-end close activities. Lead the preparation of revenue-related disclosures for the Company's Forms 10-Q and 10-K. Prepare and maintain SOX-compliant controls for the revenue and accounts receivable cycles, ensuring proper execution and documentation. Requirements Bachelor's degree in Accounting, Finance, or a related field. 5+ years of financial accounting experience, with a significant focus on revenue recognition (ASC 606). In-depth knowledge of U.S. GAAP and SOX compliance requirements as they apply to revenue recognition, receivables, contract assets and deferred revenue. Demonstrated ability to manage and execute complex monthly and quarterly close processes. Demonstrated ability to communicate complex accounting guidance clearly and effectively to non-finance and cross-functional partners. Strong capability to lead change initiatives and successfully manage complex, multi-phase projects. Strong organizational skills, with a focus on accuracy, detail orientation and the ability to produce in tight timelines. Strong interpersonal, oral and written communication skills. Possess the highest level of integrity. Ability to adapt to a rapidly changing environment. Excellent team player. Self-motivated with an insatiable desire to learn and be challenged. Ability for occasional travel between locations. Preferred Demonstrated experience in a technical accounting role within the life sciences, biotech, or pharmaceutical industry. Big 4 accounting firm experience. Public company experience. California pay range $120,000—$145,000 USD. Arrowhead provides competitive salaries and an excellent benefit package. Candidates must have current, valid authorization to work in the country where this role is located. California Applicant Privacy Policy.

🏢 Summary: Corporate Counsel role focused on market access, pricing, reimbursement, trade, and distribution legal support for pharmaceutical products in U.S. and global markets. The position involves advising on government pricing programs, payer and PBM agreements, compliance, and commercialization strategies while collaborating across legal and commercial teams. Based in Pasadena, CA, this in-office role also includes contract negotiation, regulatory guidance, and risk mitigation responsibilities. 🗂️ Requirements: 3+ years experience in trade and distribution, government pricing, payer contracting, or related pharmaceutical legal practice, J.D. degree, Licensed to practice law in the U.S., Permitted to practice law in California, Active state bar membership in good standing, Knowledge of fraud and abuse laws related to payer and PBM agreements, Experience with pharmaceutical pricing, reimbursement, and market access issues, Knowledge of Medicaid Drug Rebate Program, 340B, and Federal Supply Schedule, Understanding of pharmaceutical sales and marketing regulatory frameworks, Strong legal communication and risk assessment skills, Ability to manage competing priorities in a fast-paced environment, Authorization to work in the country where the role is located 📃 Skills: RNAi, FDA, PBM, 340B, Medicaid, Medicare, MLR, Contracting, Reimbursement, Pricing, Compliance, Distribution, Regulatory 🏢 Description: Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company developing RNAi-based therapies for diseases with a genetic basis. The company focuses on innovative drugs targeting conditions involving overproduction of disease-related proteins, with programs in liver and lung diseases and a growing preclinical pipeline. The Corporate Counsel (Market Access and Pricing) will report to the Assistant General Counsel and provide strategic, business-focused legal and risk counseling related to pricing, reimbursement, market access, trade, and distribution activities for U.S. and global markets. The role involves close collaboration with legal, commercial, and contracts teams to support commercialization strategies and ensure compliance with healthcare laws and regulations. This role is based in Pasadena, California, with an expectation to be in office 5 days a week. Responsibilities - Provide strategic counsel on drug pricing, reimbursement, and market access issues - Serve as an enterprise expert on federal supply schedule contracting and federal/state pricing requirements - Advise on compliance with government price laws, including Medicaid Drug Rebate Program, Medicare Part D Manufacturer Discount Program, and 340B program requirements - Advise on arrangements and interactions with pharmacy benefit managers, health plans, employers, governments, and other payers - Provide legal guidance on trade and distribution strategies, patient support programs, state price reporting, rebate and discount arrangements, value-based agreements, and payer communications - Negotiate and draft agreements related to market access and pricing activities - Provide legal oversight for third-party contractors handling market access, invoicing, price reporting, and distribution services - Manage outside counsel regarding ex-US requirements - Serve as a secondary legal representative on the Medical Legal Regulatory (MLR) Review Committee - Support FDA promotional law matters, medical and marketing interactions, and healthcare compliance strategies - Engage with government or regulatory agencies regarding policy implications and legal perspectives - Prepare and deliver organizational training on contracting and risk mitigation Requirements - 3 years of experience involving trade and distribution, government pricing, payer contracting, or related fields in a law firm, pharmaceutical company, or medical device company - J.D. degree and license to practice law in the U.S. - Permission to practice law in California, including as Registered In-House Counsel - Active state bar membership in good standing - Deep knowledge of fraud and abuse laws related to payer and PBM agreements - Experience with competition, pricing, reimbursement, and market access issues in the pharmaceutical industry - Knowledge of government pricing programs including Medicaid Drug Rebate Program, 340B, and Federal Supply Schedule - Understanding of statutory and regulatory frameworks governing pharmaceutical sales and marketing - Strong oral and written communication skills - Strong analytical, strategic thinking, and time management abilities - Business acumen and ability to provide practical, risk-based legal advice - Conflict resolution and collaboration skills in a global environment Benefits - California pay range: $200,000—$260,000 USD - Competitive salary and benefits package - Opportunity to develop additional legal practice areas within a small legal department Candidates must have current, valid authorization to work in the country where this role is located.

🏢 Summary: Senior Scientist role focused on integrating human genetics, multi-omics, and real-world clinical data to support therapeutic target validation, patient stratification, and drug development. The position involves analyzing biobank-scale datasets, EHRs, and population data using computational and statistical methods in a cross-functional research environment. This onsite role in San Diego emphasizes translational genetics, RWE analytics, and scalable data workflows for precision medicine. 🗂️ Requirements: PhD in Biostatistics, Statistical Genetics, Epidemiology, Bioinformatics, Computational Biology, Biomedical Data Science, or related quantitative field, 3+ years of experience in human genetics, biomedical data science, or real-world data analytics, Experience with AI/LLMs for coding, data analysis, literature synthesis, and report generation, Experience working with biobank-scale datasets and real-world data sources, Strong background in statistical genetics, epidemiology, or observational data analysis, Experience integrating genetics, omics, and clinical datasets, Proficiency in R or Python, Ability to work in a fast-paced cross-functional research environment, Valid authorization to work in the country where the role is located 📃 Skills: R, Python, AI, LLMs, RNAi, EHR, OMOP, OHDSI, PheWAS, Biostatistics, Bioinformatics, Epidemiology, Genetics, Omics, MachineLearning, Statistics 🏢 Description: Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company developing RNA interference (RNAi)-based therapies for diseases with a genetic basis. The company leverages RNA chemistries and delivery technologies to silence disease-causing genes and advance therapeutics across multiple disease areas. The Senior Scientist will contribute to the integration of human genetics, multi-omics datasets, and real-world clinical data to generate human evidence supporting therapeutic development. This role works at the intersection of translational genetics, computational biology, and real-world evidence analytics to support target validation, patient stratification, clinical endpoint evaluation, and indication prioritization across therapeutic programs. The successful candidate will collaborate closely with Translational Genetics & Data Science and cross-functional teams including Real-World Evidence, Clinical Development, Translational Medicine, and Discovery Biology. The role leverages large-scale biobank datasets, electronic health records (EHR), and other clinical datasets to translate human data into actionable insights supporting drug discovery and development. This position is onsite 5 days a week in San Diego. Responsibilities - Integrate human genetics, multi-omics datasets, and real-world clinical data to generate evidence supporting therapeutic target validation and indication prioritization - Analyze large-scale biobank and population datasets to identify genetic associations and disease mechanisms relevant to therapeutic programs - Collaborate with the Real-World Evidence (RWE) team to analyze clinical datasets including electronic health records (EHR), claims databases, registries, and longitudinal cohort data - Conduct statistical and computational analyses to characterize disease progression, patient heterogeneity, and treatment outcomes using real-world datasets - Translate genetic findings and clinical observations into hypotheses that inform biomarker strategies, patient stratification, and clinical trial design - Develop scalable analytical workflows to integrate genetics, omics, and clinical data sources - Work collaboratively with cross-functional teams including Discovery Biology, Clinical Development, Translational Medicine, and Data Science to support program decisions - Present results to internal stakeholders and contribute to reports, project discussions, and scientific publications - Manage multiple projects simultaneously and communicate progress and findings effectively to project teams and leadership - Adhere to data governance and compliance standards when working with sensitive clinical datasets Requirements - PhD in Biostatistics, Statistical Genetics, Epidemiology, Bioinformatics, Computational Biology, Biomedical Data Science, or a related quantitative discipline - 3+ years of experience in human genetics, biomedical data science, or real-world data analytics - Strong experience leveraging AI/LLMs to accelerate end-to-end research workflows, including coding, data analysis, literature synthesis, and report generation - Experience working with biobank-scale datasets and real-world data sources such as EHR, claims databases, registries, or population cohorts - Strong background in statistical genetics, epidemiology, or observational data analysis - Experience integrating genetics, omics, and clinical datasets - Proficiency in R or Python for large-scale data analysis - Excellent problem-solving, analytical, and communication skills - Ability to work effectively in a fast-paced, collaborative, and cross-functional research environment Preferred - Post-doc and industry experience - Experience analyzing large-scale population genetics datasets such as UK Biobank, FinnGen, All of Us, or Genomics England - Familiarity with analytical frameworks including phenome-wide association studies (PheWAS), Mendelian randomization, causal inference methods, and survival analysis - Experience working with real-world clinical data models such as OMOP / OHDSI - Experience collaborating with clinical development or real-world evidence teams - Experience applying machine learning or advanced statistical methods to biomedical datasets - Strong interest in translating human data into actionable insights for drug development Benefits - Competitive salary range: $145,000—$165,000 USD - Excellent benefits package - Candidates must have current, valid authorization to work in the country where this role is located

🏢 Summary: Full-time onsite Associate Medical Director/Medical Director role focused on advancing RNAi-based cardiometabolic therapies from late-stage clinical research through regulatory submissions. The position involves leading clinical study design, safety monitoring, data interpretation, and cross-functional collaboration for cardiac, lipid, and obesity programs. 🗂️ Requirements: M.D. or MD/Ph.D., Research experience in pharmaceutical, biotechnology, or academic settings, Hands-on translational research experience, Understanding of drug development processes, Knowledge of Good Clinical Practices, Knowledge of FDA regulations and regulatory requirements, Ability to evaluate external scientific advice, Strong scientific and medical communication skills, Ability to work independently in a fast-paced team environment, Project management skills, Strong clinical, scientific, and technical skills, Valid work authorization in the country where the role is located 📃 Skills: RNAi, siRNA, GCP, FDA, NDA, MAA, IRB, Biometrics, ClinicalTrials, Regulatory, Pharmacology, Cardiology, Endocrinology 🏢 Description: Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company focused on developing RNA interference (RNAi)-based therapies for genetically driven diseases. The Associate Medical Director/Medical Director will report to the head of cardiometabolic clinical development and will be instrumental in bringing new RNAi therapies to patients. This individual will collaborate with scientific and clinical teams to advance drugs from late-stage clinical research through NDA filings, with an initial focus on siRNA programs targeting cardiac and metabolic indications including lipids and obesity. This is a full-time onsite position based at the corporate headquarters in Pasadena, CA. Responsibilities - Support the conceptualization, design, development, execution, and communication of clinical studies across therapeutic areas - Act as a medical lead within cross-functional teams including medical, scientific, clinical, safety, program management, and regulatory staff - Communicate protocols and study information with clinical site investigators and staff - Interpret clinical trial data and communicate results accurately - Provide ongoing clinical monitoring including eligibility assessment, toxicity management, and drug safety surveillance - Contribute to IRB submissions, protocols, study reports, publications, and regulatory submissions including NDA/MAA filings - Provide scientific and clinical guidance to Clinical Trials Management, Biometrics, Global Drug Safety, Regulatory, and Project Management teams - Identify key opinion leaders and participate in advisory board meetings - Deliver scientific presentations at advisory boards and scientific meetings - Identify and evaluate medical needs and new applications of RNA interference therapies - Monitor developments in RNA interference across industry and academia - Support licensing activities and partner relationships Requirements - M.D. or MD/Ph.D. with research experience - Hands-on translational research experience in pharmaceutical, biotechnology, or academic environments - Understanding of the drug development process - Knowledge of Good Clinical Practices, FDA regulations, and regulatory requirements - Ability to evaluate expert scientific advice - Strong written and verbal scientific communication skills - Ability to work independently in a fast-paced team environment - Strong clinical, scientific, and technical skills - Strong interpersonal and collaboration skills - Sense of urgency with problem-solving initiative - Project management skills and results-oriented mindset Preferred - Fellowship training in cardiology or endocrinology - Research focused on lipids or obesity Benefits - Competitive salary and benefits package - California pay range: $260,000–$310,000 USD - Candidates must have valid authorization to work in the country where the role is located.

🏢 Summary: Senior Regulatory Affairs leadership role responsible for driving global labeling strategy and managing end-to-end regulatory labeling activities across development and post-approval phases. The position leads cross-functional collaboration, ensures compliance with global regulatory requirements, and oversees preparation, review, and maintenance of core and regional labeling documents. It also supports health authority interactions, policy development, and continuous improvement of labeling processes. 🗂️ Requirements: Bachelor's degree in life sciences, computer science, or related science discipline, Minimum 8+ years in biotech or pharmaceutical industry managing product labeling across at least two major geographic regions, Experience developing and maintaining global regulatory labeling throughout all development phases, Knowledge of FDA guidance documents and advertising promotion regulations, Experience negotiating with regulatory authorities and leading cross-functional discussions, Ability to review and ensure accuracy and compliance of regulatory labeling documents, Strong knowledge of MS Word formatting, PDF compliance, and validation tools, Valid work authorization in the country where the role is located 📃 Skills: Regulatory, Labeling, FDA, CCDS, USPI, SmPC, Veeva, RIM, AI, MSWord, PDF 🏢 Description: Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage regulatory labeling through all phases of development and post-approval (end-to-end) ensuring that the latest requirements and standards are met. The ideal candidate will have experience collaborating with product and clinical development, medical, market access, and commercial stakeholders to generate phase and time-appropriate target product profile and labeling drafts, has successfully negotiated with health authorities, and global regulatory experience. Responsibilities Collaborate cross-functionally to develop labeling strategy and lead cross-functional Labeling meetings. Manage development, review, approval, and version control of labeling documents, including Target Product Labeling, Core Labeling (e.g., Company Core Data Sheet [CCDS]), and Regional Labeling (e.g., USPI, EU SmPC), in a timely manner according to internal SOPs and external regulatory requirements. Maintain expertise regarding key labeling requirements and stay current with labeling guidelines/regulations as they pertain to the development/maintenance of labeling and advise key stakeholders on the application of these labeling principles. Research the content of other labels in the same therapeutic class, including competitor labeling, to help guide the team in developing labeling text, including contingency strategy development for negotiation with regulatory authorities. Responsible for proofreading and departmental QC work; ensure quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency between labeling documents). Liaise with cross functional members and stakeholders to obtain input pertaining to labeling including resolution of key regulatory issues and labeling changes . Partner with Clinical Regulatory and cross-functional teams to support labeling supplements and updates, and health authority interactions related to labeling Ensure the dissemination of approved labeling documents and supporting documentation. Maintain controlled records for all labeling changes and communicate labeling updates to stakeholders at the time of implementation. Build partnerships with key stakeholders from other functions to ensure that strategic business goals are met through the sharing of knowledge and expertise. Participate in any relevant continuous improvement efforts for the end-to-end labeling process. Monitor global regulatory environment and assess impact of changes on business and product labeling activities. Facilitate policy development and updates with internal stakeholders. Requirements Bachelor's degree in life sciences, computer science, or related science discipline Minimum 8+ in the biotech or pharmaceutical industry leading the development/maintenance of product labeling across two or more major geographic areas. Knowledge of advertising promotion regulations and FDA Guidance documents issued with some technical experience in aspects of drug development and labeling Experience leading cross-functional meetings and facilitating strategic discussions, such as negotiating with internal stakeholders and regulatory authorities on complex labeling issues. Ability to review regulatory labeling documents for accuracy and adherence to regulatory requirements, noting deviations and inconsistencies. Strong knowledge of document formatting (MS Word documents, PDFs compliance, and validation tools) Ability to maintain highest degree of professionalism, integrity and diplomacy Preferred Experience with regulatory information management systems (e.g., Veeva RIM, Registrations). Knowledgeable in emerging technologies, including AI applications in regulatory operations. Experience supporting global inspection readiness. California pay range $210,000—$230,000 USDArrowhead provides competitive salaries and an excellent benefit package. Candidates must have current, valid authorization to work in the country where this role is located. California Applicant Privacy Policy

🏢 Summary: Director of Regulatory Affairs role responsible for leading global labeling strategy and execution across all development phases and post-approval activities. The position manages end-to-end regulatory labeling processes, collaborates cross-functionally, and ensures compliance with global regulatory requirements. It requires extensive experience in biotech/pharma labeling, health authority negotiations, and regulatory documentation management. 🗂️ Requirements: Bachelor's degree in life sciences, computer science, or related science discipline, Minimum 8+ years in biotech or pharmaceutical industry leading product labeling across at least two major geographic areas, Knowledge of advertising promotion regulations and FDA Guidance documents, Experience negotiating with regulatory authorities on complex labeling issues, Ability to review regulatory labeling documents for accuracy and regulatory compliance, Strong knowledge of document formatting and compliance tools (MS Word, PDF validation tools), Valid work authorization in the country where the role is located 📃 Skills: Regulatory, Labeling, FDA, CCDS, USPI, SmPC, Veeva, RIM, MSWord, PDF, AI 🏢 Description: Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage regulatory labeling through all phases of development and post-approval (end-to-end) ensuring that the latest requirements and standards are met. The ideal candidate will have experience collaborating with product and clinical development, medical, market access, and commercial stakeholders to generate phase and time-appropriate target product profile and labeling drafts, has successfully negotiated with health authorities, and global regulatory experience. Responsibilities Collaborate cross-functionally to develop labeling strategy and lead cross-functional Labeling meetings. Manage development, review, approval, and version control of labeling documents, including Target Product Labeling, Core Labeling (e.g., Company Core Data Sheet [CCDS]), and Regional Labeling (e.g., USPI, EU SmPC), in a timely manner according to internal SOPs and external regulatory requirements. Maintain expertise regarding key labeling requirements and stay current with labeling guidelines/regulations as they pertain to the development/maintenance of labeling and advise key stakeholders on the application of these labeling principles. Research the content of other labels in the same therapeutic class, including competitor labeling, to help guide the team in developing labeling text, including contingency strategy development for negotiation with regulatory authorities. Responsible for proofreading and departmental QC work; ensure quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency between labeling documents). Liaise with cross functional members and stakeholders to obtain input pertaining to labeling including resolution of key regulatory issues and labeling changes . Partner with Clinical Regulatory and cross-functional teams to support labeling supplements and updates, and health authority interactions related to labeling Ensure the dissemination of approved labeling documents and supporting documentation. Maintain controlled records for all labeling changes and communicate labeling updates to stakeholders at the time of implementation. Build partnerships with key stakeholders from other functions to ensure that strategic business goals are met through the sharing of knowledge and expertise. Participate in any relevant continuous improvement efforts for the end-to-end labeling process. Monitor global regulatory environment and assess impact of changes on business and product labeling activities. Facilitate policy development and updates with internal stakeholders. Requirements Bachelor's degree in life sciences, computer science, or related science discipline Minimum 8+ in the biotech or pharmaceutical industry leading the development/maintenance of product labeling across two or more major geographic areas. Knowledge of advertising promotion regulations and FDA Guidance documents issued with some technical experience in aspects of drug development and labeling Experience leading cross-functional meetings and facilitating strategic discussions, such as negotiating with internal stakeholders and regulatory authorities on complex labeling issues. Ability to review regulatory labeling documents for accuracy and adherence to regulatory requirements, noting deviations and inconsistencies. Strong knowledge of document formatting (MS Word documents, PDFs compliance, and validation tools) Ability to maintain highest degree of professionalism, integrity and diplomacy Preferred Experience with regulatory information management systems (e.g., Veeva RIM, Registrations). Knowledgeable in emerging technologies, including AI applications in regulatory operations. Experience supporting global inspection readiness. California pay range $210,000—$230,000 USDArrowhead provides competitive salaries and an excellent benefit package. Candidates must have current, valid authorization to work in the country where this role is located. California Applicant Privacy Policy

🏢 Summary: Field-based Medical Science Liaison role focused on cardiometabolic diseases, supporting scientific engagement with healthcare professionals and advancing RNAi-based therapies. The position involves clinical education, scientific exchange, congress participation, and support for Medical Affairs initiatives and clinical trials. Candidates must have extensive MSL and cardiometabolic experience within biotech or pharmaceutical environments. 🗂️ Requirements: PhD, PharmD, MD, or DO degree, 5+ years of MSL experience, Cardiometabolic therapeutic experience, Medical Affairs experience in biotech or pharma, Strong verbal and written communication skills, Ability to interpret and communicate scientific data, Knowledge of healthcare delivery and managed care systems, Understanding of clinical research study design and execution, Project management skills, Ability to travel, Valid work authorization 📃 Skills: RNAi, MedicalAffairs, Cardiometabolic, Hypertriglyceridemia, Hypercholesterolemia, ClinicalTrials, Pharmacology, Endocrinology, Cardiology, Research, ManagedCare, ProjectManagement 🏢 Description: Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company developing RNAi-based medicines for diseases caused by gene overexpression. The company develops therapies that leverage RNA interference mechanisms to induce targeted gene silencing across multiple therapeutic areas, including liver and lung diseases. The Position We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join the Medical Affairs team in a field-based role. Candidates must be located within one of the assigned territories. MSLs are responsible for developing professional relationships with healthcare professionals through scientific engagement to support clinical stage and launch molecules. The role includes scientific exchange, clinical support, and collaboration with internal stakeholders. Responsibilities - Engage with cardiologists, endocrinologists, healthcare professionals, and stakeholders to educate on clinical and scientific evidence aligned with strategic imperatives - Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia - Synthesize and communicate clinical and scientific insights to internal stakeholders - Attend and present at scientific congresses and meetings to remain current on cardiometabolic developments - Respond to unsolicited inquiries consistent with MSL compliance standards - Support company-sponsored clinical trials through investigator site engagement - Support speaker training and ensure speakers remain current on disease and product data - Support national, regional, and local scientific congresses including opinion leader engagement and session coverage - Monitor and analyze scientific publications, clinical trials, and the competitive landscape in cardiometabolic therapeutics - Maintain clinical and scientific expertise and industry business acumen - Develop territory-specific opinion leader and account plans - Communicate clinical and scientific information accurately and clearly - Document quantitative and qualitative accomplishments - Provide scientific support for medical information inquiries - Develop scientific content for medical education initiatives - Support Medical Affairs special projects and initiatives - Collaborate cross-functionally across teams - Act in accordance with company policies Requirements - PhD, PharmD, MD, or DO degree required - 5 years of experience as an MSL - Cardiometabolic therapeutic experience - Industry experience in Medical Affairs at a biotech or pharmaceutical company - High level verbal and written communication skills - Ability to collaborate effectively in a dynamic environment - Strong understanding of the cardiometabolic therapeutic area - Ability to interpret scientific data and translate findings into educational and research insights - Ability to identify unmet medical, educational, and research needs in the medical community - Understanding of healthcare delivery systems and managed care - Understanding of research study design and execution - Strategic thinking and ability to drive high-quality results - Ability to manage ambiguity and adapt to changing environments - Strong project management, organizational, and time management skills - Ability to travel - Current valid authorization to work in the country where the role is located Benefits - Competitive salary range of $190,000–$210,000 USD - Comprehensive benefits package

🏢 Summary: Field-based Medical Science Liaison role focused on cardiometabolic diseases, supporting scientific engagement with healthcare professionals and advancing RNAi-based therapies. The position involves clinical education, stakeholder relationship management, scientific congress participation, and support for clinical trials and Medical Affairs initiatives. 🗂️ Requirements: PhD, PharmD, MD, or DO degree, 5+ years of MSL experience, Cardiometabolic therapeutic area experience, Medical Affairs experience in biotech or pharma, Strong verbal and written communication skills, Ability to interpret and communicate scientific data, Understanding of healthcare delivery systems and managed care, Knowledge of research study design and execution, Project management and organizational skills, Ability to travel, Valid work authorization in the country of employment 📃 Skills: RNAi, MedicalAffairs, Cardiometabolic, ClinicalTrials, Hypertriglyceridemia, Hypercholesterolemia, PharmD, PhD, MD, DO 🏢 Description: Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company focused on developing RNAi-based therapies for diseases with a genetic basis. We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join the Medical Affairs team in a field-based role. Candidates must be located within one of the designated territories. Responsibilities - Engage with cardiologists, endocrinologists, healthcare professionals, and stakeholders to educate on clinical and scientific evidence aligned with strategic imperatives - Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia - Synthesize and communicate clinical and scientific insights to internal stakeholders - Attend and present at scientific congresses and meetings to stay current with developments in the cardiometabolic therapeutic area - Respond to unsolicited inquiries consistent with MSL compliance standards - Support company-sponsored clinical trials through investigator site engagement - Support speaker training and ensure speakers remain current with evolving disease and product data - Support scientific congresses including opinion leader engagement, session coverage, booth activities, and debriefs - Monitor and analyze scientific publications, clinical trials, and competitive landscape in the cardiometabolic therapeutic area - Maintain clinical and scientific expertise and industry business acumen - Develop territory-specific opinion leader and account plans - Communicate clinical and scientific information accurately and clearly - Document quantitative and qualitative accomplishments - Provide scientific support for Medical Information inquiries - Develop scientific content for medical education initiatives - Support Medical Affairs special projects and initiatives - Collaborate cross-functionally in a dynamic environment - Act in accordance with company policies Requirements - PhD, PharmD, MD, or DO degree required - 5 years of experience as an MSL - Cardiometabolic therapeutic experience - Industry experience in Medical Affairs at a biotech or pharma company - Strong verbal and written communication skills - Ability to collaborate effectively in a dynamic environment - Strong comprehension of the cardiometabolic therapeutic area - Ability to interpret scientific data and translate findings into educational and research insights - Ability to identify unmet medical, educational, and research needs within the medical community - Understanding of healthcare delivery systems and managed care - Understanding of research study design and execution - Proven strategic thinking and ability to drive results - Ability to thrive in an evolving environment - Strong project management, time management, and organizational skills - Ability to travel - Current valid authorization to work in the country where the role is located Benefits - Competitive salary range: $190,000–$210,000 USD - Excellent benefits package

🏢 Summary: Field-based Medical Science Liaison role focused on cardiometabolic diseases, supporting scientific engagement with healthcare professionals and advancing RNAi-based therapies through education, clinical support, and medical affairs collaboration. The position involves working with cardiologists and endocrinologists, supporting clinical trials, presenting scientific data, and contributing to medical education initiatives. 🗂️ Requirements: PhD, PharmD, MD, DO, 5+ years MSL experience, Cardiometabolic therapeutic experience, Medical Affairs experience in biotech or pharma, Strong verbal and written communication skills, Ability to interpret scientific data, Understanding of healthcare delivery systems and managed care, Research study design and execution knowledge, Project management skills, Ability to travel, Valid work authorization 📃 Skills: RNAi, Cardiometabolic, MedicalAffairs, ClinicalTrials, Endocrinology, Cardiology, Research, ProjectManagement, ManagedCare, Biotech, Pharma 🏢 Description: Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company developing RNAi-based medicines for genetically driven diseases. The Position We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join our Medical Affairs team in a field-based role. Candidates must be located within one of the assigned territories. MSLs are responsible for developing professional relationships with healthcare professionals through scientific engagement to support clinical stage and launch molecules. MSLs engage healthcare professionals through scientific exchange and provide clinical and scientific support. Responsibilities - Engage with cardiologists, endocrinologists, healthcare professionals, and stakeholders to educate on clinical and scientific evidence aligned with strategic imperatives - Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia - Synthesize and communicate clinical and scientific insights to internal stakeholders - Attend and present at scientific congresses and meetings to stay current with developments in the cardiometabolic therapeutic area - Respond to unsolicited inquiries consistent with MSL compliance standards - Support company-sponsored clinical trials through investigator site engagement - Support speaker training and ensure speakers remain up to date with disease and product data - Support scientific congresses including Opinion Leader engagement, session coverage, booth support, and company debriefs - Monitor and analyze scientific publications, clinical trials, and the competitive landscape in cardiometabolic therapeutics - Maintain clinical and scientific expertise and industry business acumen - Develop territory-specific Opinion Leader and account plans - Communicate clinical and scientific information accurately and clearly - Document quantitative and qualitative accomplishments - Provide scientific support for medical information inquiries - Develop scientific content for medical education initiatives - Support Medical Affairs projects and initiatives - Build and maintain strong cross-functional relationships - Act in accordance with company policies Requirements - PhD, PharmD, MD, or DO degree required - 5 years of experience as an MSL - Cardiometabolic therapeutic experience - Industry experience in Medical Affairs at a biotech or pharmaceutical company - Strong verbal and written communication skills - Ability to collaborate effectively in a dynamic environment - Strong understanding of the cardiometabolic therapeutic area - Ability to interpret scientific data and translate findings into educational and research insights - Ability to identify unmet medical, educational, and research needs - Understanding of healthcare delivery systems and managed care - Understanding of research study design and execution - Strategic thinking and ability to deliver high-quality results - Ability to manage ambiguity in a changing environment - Strong project management, organizational, and time management skills - Ability to travel - Current valid authorization to work in the country where the role is located Benefits - Competitive salary range: $190,000–$210,000 USD - Excellent benefits package

🏢 Summary: The Information Security Systems Analyst is responsible for administering and optimizing Microsoft Purview to ensure effective data governance, data loss prevention, and information protection within a regulated environment. The role focuses on managing sensitivity labels, DLP policies, eDiscovery, and insider risk management while supporting broader Microsoft 365 security operations. It involves monitoring compliance, investigating alerts, and collaborating with cross-functional teams to protect sensitive and regulated data. 🗂️ Requirements: Bachelor's degree in Information Security, Information Technology, Computer Science or related field or equivalent experience, 3+ years of experience in Information Security, IT compliance, or data governance, Hands-on experience administering Microsoft Purview or Microsoft 365 Compliance Center, Experience with at least two of the following: sensitivity labels, DLP, retention policies, eDiscovery, Insider Risk Management, Experience working in a regulated industry environment, Ability to investigate security alerts and interpret audit logs, Valid work authorization in the country of employment 📃 Skills: MicrosoftPurview, Microsoft365, DLP, eDiscovery, InsiderRiskManagement, Intune, Exchange, SharePoint, OneDrive, Teams, AuditLogs, SIEM, EDR, IAM, MCAS 🏢 Description: The Information Security Systems Analyst is responsible for the day-to-day administration, operation, and continuous improvement of the organization's Microsoft Purview platform, serving as the primary subject matter expert for data governance, data loss prevention (DLP), and information protection. This role operates at the intersection of information security, data governance, and regulatory compliance, ensuring that sensitive data - including intellectual property, clinical trial data, and personally identifiable information - is properly classified, protected, and governed in accordance with applicable regulations and internal policies. In addition to Purview-focused responsibilities, this analyst contributes to broader information security operations including troubleshooting endpoints, working in Microsoft 365, and Intune. Responsibilities The analyst will serve as the hands-on operational owner of Microsoft Purview, managing the platform on a daily basis across its core functional areas: Information Protection & Data Classification - Administer and maintain Microsoft Purview sensitivity labels, label policies, and auto-labeling configurations - Develop and refine classification taxonomies appropriate to pharmaceutical data types, including research data, regulatory submissions, and patient data - Review and tune auto-classification rules to minimize false positives and ensure accurate labeling across Microsoft 365 and connected data sources Data Loss Prevention - Build, maintain, and continuously tune DLP policies across Exchange, SharePoint, OneDrive, Teams, and endpoints - Investigate DLP policy matches and alerts, differentiate true policy violations from false positives, and refine rules without disrupting legitimate workflows - Document DLP incidents and escalate confirmed violations per the incident response process E-Discovery & Content Search - Support legal hold requests and eDiscovery collections - Work with Legal and HR to scope, execute, and export content searches in accordance with chain-of-custody requirements Insider Risk Management - Administer Purview Insider Risk Management policies and review alerts - Coordinate with HR, Legal, and Security leadership on confirmed or suspected insider risk cases - Maintain strict confidentiality in handling insider risk data Audit & Reporting - Generate and interpret Purview audit logs, compliance reports, and dashboard analytics - Provide regular reporting on DLP incidents, label adoption rates, policy effectiveness, and compliance posture - Identify trends and recommend adjustments to policies and configurations Platform Administration & Health Monitoring - Monitor the health and performance of the Purview platform - Apply configuration changes and updates in alignment with change management processes - Manage connector integrations with third-party data sources - Maintain clear documentation including runbooks, diagrams, standards, and exceptions - Triage security alerts and escalate as necessary Requirements - Bachelor's degree in Information Security, Information Technology, Computer Science, or related field, or equivalent practical experience - 3+ years of experience in Information Security, IT compliance, or data governance - Demonstrated hands-on experience administering Microsoft Purview or Microsoft 365 Compliance Center, including at least two of the following: sensitivity labels, DLP, retention policies, eDiscovery, or Insider Risk Management - Experience working within or supporting a regulated industry environment - Strong analytical and problem-solving skills - Effective written and verbal communication skills - Current, valid authorization to work in the country where this role is located Preferred - Microsoft certifications relevant to security and compliance such as SC-401 - Experience with Microsoft Defender for Cloud Apps (MCAS) - Experience supporting eDiscovery or legal hold workflows - Exposure to SIEM tools, endpoint detection and response (EDR) platforms, or identity and access management systems Compensation Wisconsin pay range $85,000—$100,000 USD California pay range $95,000—$110,000 USD Arrowhead provides competitive salaries and an excellent benefit package.