Clinical Research Project Coordinator
2 weeks ago
About Advarra:
Advarra is dedicated to enhancing the safety, efficiency, and speed of clinical research. Our comprehensive solutions are designed to protect trial participants, empower clinical sites, ensure regulatory compliance, and optimize research outcomes for a diverse range of sponsors, CROs, institutions, academic medical centers, and research consortia.
With unparalleled independent oversight committee services, innovative software solutions tailored for sites, sponsors, and CROs, and a team of seasoned consultants with extensive industry connections, Advarra possesses the expertise and technology necessary to propel clinical research forward and assist our clients in creating a healthier world.
About the Opportunity:
Are you interested in collaborating with skilled and dedicated clinical research professionals?
Advarra is looking for a part-time Clinical Research Coordinator II to work onsite. This is a consulting (contractor) position for a duration of 6 months and does not include benefits.
Role Overview: The Clinical Research Coordinator II will be responsible for planning, directing, and coordinating clinical research initiatives while also evaluating and analyzing clinical data.
Qualifications:
- A Bachelor's degree with three (3) years of relevant experience in clinical, health-related, scientific, business, or research fields, or an Associate's degree with four (4) years of relevant experience.
- Preferred certifications include Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or Society of Clinical Research Associates (SOCRA).
- Current training in human subjects protection, Good Clinical Practice, and HIPAA Privacy regulations.
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