CLINICAL RESEARCH COORDINATOR III
Job description
To manage all aspects of assigned clinical studies including education. To develop protocol-specific systems and documents. To act as a consultant within area of clinical expertise. To identify various stakeholders to ensure adequate design, implementation, and testing of study aims. To assess and determine solutions for operational shortcomings for data procurement in protocol design. To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.
Duties and Responsibilities:
- Collects data via surveys, interviews, and medical record extraction.
- Coordinates collection of biospecimens.
- Enrolls and maintains engagement with study participants.
- Coordinates participant recruitment with study physicians.
- Submits protocol amendments to IRBR.
- Review Data managements system for completion and errors of survey data.
- Assist with electronic and hard copy research data management.
- Perform other duties as assigned.
Annual Salary Range: $60,835 - $98,855
Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement.
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.
Additional Skills Preferred:
- Excellent organizational skills with great attention to detail.
- Capable of independent as well as collaborative work.
- Excellent documentation skills.
- Effective interpersonal and communication skills.
- Proficiency in all MS Office applications
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