Advarra is a global leader in clinical research, dedicated to advancing human health through ethical review services, innovative technology, and deep industry expertise. The company bridges gaps in clinical trials by connecting patients, sites, sponsors, and CROs in a unified ecosystem to accelerate research.
Why Join Advarra?
- Mission-Driven Work: Contribute to advancing clinical research that improves lives.
- Inclusive Culture: A collaborative environment that values diversity, equity, and inclusion.
- Professional Growth: Opportunities to work with cutting-edge clinical trial management tools.
Job Description: Research Associate III
Key Responsibilities
- Interpret clinical trial protocols to design study calendars and budgets.
- Develop case report forms (CRFs) for clinical studies.
- Utilize Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems.
- Collaborate with managers to ensure high-quality deliverables.
- Track and report work progress using internal case management tools.
- Participate in team discussions to enhance project outcomes.
Basic Qualifications
- 2+ years of experience in clinical research.
- Knowledge of Good Clinical Practice (GCP) and clinical trial regulations.
- Proficiency in MS Office and business software.
- Strong organizational and teamwork skills.
Preferred Qualifications
- Experience as a clinical trial coordinator, data manager, or pharmacovigilance professional.
- Background in records management or clinical operations.
