Senior Clinical Research Coordinator
3 days ago
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OnsitePart-timeMid
Summary
Advarra is seeking a Senior Clinical Research Coordinator to join their team in Brick, NJ. The role involves planning, directing, and coordinating clinical research projects while evaluating and analyzing clinical data.
About the Role
As a Senior Clinical Research Coordinator, you will be responsible for overseeing clinical research projects, ensuring compliance with regulations, and collaborating with various stakeholders to optimize research performance. This position requires onsite work two days per week and is a consulting role without benefits.
About You
Required:
- Bachelor’s degree with three (3) years of relevant clinical, health related, scientific, business or research experience or Associate’s degree with four (4) years of relevant experience.
- Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy.
Preferred:
- Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Associates (SOCRA) certifications or equivalent.
Benefits
- Part-time consulting role with flexible hours.
- Opportunity to work with a talented team of clinical research professionals.
Advarra
Advarra advances the way clinical research is conducted: bringing life sciences companies, CROs, research sites, investigators, and academia together at the intersection of safety, technology, and collaboration. With trusted IRB and IBC review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra provides integrated solutions that safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance. Advarra is advancing clinical trials to make them safer, smarter, and faster. For more information, visit advarra.com.
Brick, NJ