Clinical Research Coordinator II

Quick Facts

• Role: Clinical Research Coordinator II

• Schedule: Full Time, 40 hours/week (Monday–Friday)

• Shift: Days

• Weekend requirements: None

Description

Collects, compiles, and presents clinical data for assigned programs, ensuring accuracy, timeliness, and accessibility. Maintains clinical and/or research databases for specialty clinics and supports activities that may include process improvement, clinical effectiveness research studies, and patient/family education or community outreach.

Responsibilities

• Collect, compile, and present clinical research data

• Ensure data accuracy, timeliness, and accessibility

• Maintain clinical and research databases

• Support process improvement and clinical effectiveness/research studies

• Prepare information for patient/family education and/or participate in community outreach (as needed)

Requirements

• Bachelor's in Science or health-related field (equivalent experience accepted)

• 2 years of recent relevant experience

• Knowledge of federal and state regulations and international guidelines related to GCP

• Ability to interpret data and instructions from multiple formats

• Written and verbal communication skills for working with teams, supervisors, patients, and hospital personnel

• Strong time management and organizational skills; ability to prioritize and meet deadlines

• Computer skills, including Microsoft Office Suite (Word, Excel, Access, PowerPoint)

Benefits

Benefits available