What are the responsibilities and job description for the Clinical Research Coordinator position at Advarra?
About Advarra:
Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance for over 3,500 sponsors, CROs, institutions, academic medical centers, and research consortia.
With trusted and unequaled independent oversight committee services, innovative software solutions for sites, sponsors, and CROs, and experienced consultants with deep-seated connections across the industry, Advarra has the expertise and technology needed to advance clinical research and help our clients make the world a healthier place.
About the Opportunity:
Do you have an interest in joining talented and passionate clinical research professionals?
Advarra is seeking a part-time and full-time Clinical Research Coordinator II to work onsite in the New York area. This is a consulting (contractor) role and does not include benefits.
Clinical Research Coordinator II
The Clinical Research Coordinator II will plan, direct, and coordinate clinical research projects along with evaluating and analyzing clinical data.
Credentials and Qualifications:
- Experience with biological lab experiments
- 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 clinical, health related, scientific, business or research experience.
- Certified Clinical Research Professional (CCRP)/Certified Clinical Research Coordinator (CCRC)/Society of Clinical Research Associates (SOCRA) certifications or equivalent preferred
- Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
