Clinical Research Physician (Principal Investigator)

Quick Facts

Role: Clinical Research Physician (Principal Investigator)

Schedule: Monday through Friday

Description

You will conduct and coordinate daily clinical trial activities at the site as Principal Investigator, ensuring participant safety and ethical execution in accordance with FDA, ICH, GCP, and HIPAA guidelines. The role includes overall site leadership to improve efficiencies and ensure protocol/GCP/regulatory compliance, while supporting participant eligibility, study delivery, and retention.

Responsibilities

• Ensure medical well-being and safety of study participants and the ethical execution of clinical trials per FDA, ICH, NIH, GCPs, and HIPAA, as well as study protocols and company policies
• Provide overall site leadership with focus on efficiency, patient safety, and protocol/GCP/regulatory compliance
• Evaluate and assess participants to ensure only eligible participants enroll
• Support successful study delivery and participant retention
• Collaborate with sponsors, clients, and team members
• Record data and participant information accurately according to protocol and GCP
• Participate in protocol training for site staff
• Attend Investigator Meetings (IMs) and continuing education to stay current on recruitment activities and issues
• Perform other assigned duties based on participant needs, protocols, and/or site requirements

Requirements

• MD or DO degree
• Active physician license in good standing in the state of practice
• Board certification in the candidate’s specialty area
• Clinical skills and procedures within the specialty area
• Proficiency with MS Office, electronic health records, and web applications; ability to type proficiently (40+ wpm)
• Strong organizational skills and attention to detail; math proficiency
• Strong written and verbal communication skills
• High level of urgency, integrity, and dependability
• Ability to work independently to identify problems and implement solutions
• Ability to handle highly sensitive information confidentially and professionally in compliance with HIPAA
• Bilingual English/Spanish proficiency highly preferred
• Clinical research experience preferred

Benefits

• Work-life balance: sites operate Monday through Friday