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This position involves monitoring and oversight of clinical sites to ensure the timely and successful execution of clinical studies, resolving study-related discrepancies. The role includes ensuring compliance with protocol and all regulatory policies, procedures, and guidelines during clinical studies by training and guiding investigators and study coordinators, and following up on corrective actions. Additionally, the CRA will ensure the validity of the study by identifying and resolving discrepancies, obtaining missing data, and tracking routine aspects of clinical documents, which may include protocols, case report forms (CRFs), memos, correspondence, reports, and other required documents. The CRA may also conduct new CRA orientation, onboarding, and training activities.
Undertake additional projects and tasks as needed. The successful candidate will work collaboratively across cross-functional teams, including Quality, Compliance, Product Development, and Engineering. Prior experience in clinical research or clinical trials and a solid understanding of related processes are required. The role demands a quick thinker, adaptable to evolving workflows, proactive in seeking clarification, resourceful, and capable of independent work. Creativity in problem-solving and openness to innovation are valued. The candidate should learn internal processes quickly and work independently with minimal supervision, taking initiative in a fast-paced environment.
Bachelor's degree in Biology, Health Sciences, Mathematics, Computer Science, or related field. Certifications like CCDM are a plus but not required.
Pay ranges between $42-49/hr based on experience. The Planet Group of Companies is an equal opportunity employer committed to diversity and inclusion.
Employment type: Full-time
Job function: Research, Analysis, IT
Industry: Staffing and Recruiting
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