CONTRACT CLINICAL RESEARCH ASSOCIATE

A senior-level position in Clinical Research, under some supervision of Project/Program Managers this position participates in the planning, designing, and executing of high quality clinical studies to ensure safety and effectiveness of products. Candidate works with confidential patient and company data, and interfaces with a variety of internal and external stakeholders. Depending upon Clinical requirements may be directly involved in the monitoring of trials. The person in this role may be asked to represent Clinical function on teams. Based upon Clinical requirements, may monitor on-going compliance to study protocols and site adherence to global regulatory guidelines.Assists clinical project manager with developing/maintaining project timeline, managing study budget, and preparing routine operations reports.
REQUIREMENTS
Requirements: Bachelor's-level degree required. Degree in science/health related field (e.g., Biology, Nursing,
Biomedical or Veterinary Sciences) preferred. 5 years experience in clinical/scientific research, nursing, or medical devices/pharmaceutical industry required. 2-3 years of clinical monitoring experience required. Project management experience preferred. EDC experience is a must.