Remote Clinical Research Coordinator: Trials & Compliance
Thorne
South Carolina
À distance
USD 65 000 - 80 000
Plein temps
14 jours+
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Avantages offerts par ce poste
100% company-paid medical, dental, and vision insurance
401(k) plan with employer matching contributions
Gym membership reimbursement
Paid time off and holiday leave
Résumé du poste
A leading health solutions company is seeking a Research Coordinator to support clinical studies, ensuring compliance and efficiency. This role involves managing research protocols, participant interactions, and regulatory documentation. Candidates must hold a bachelor's degree in Life Sciences and have at least 5 years of experience in clinical operations. The position offers competitive compensation and comprehensive benefits, making it an excellent opportunity for those passionate about health and wellness.
Qualifications
Minimum of 5 years of experience in clinical operations roles.
Experience in designing and managing human clinical trials.
Strong understanding of IRB regulations and compliance.
Responsabilités
Support clinical research programs for new and existing products.
Manage compliance with clinical protocols and guidelines.
Coordinate participant recruitment and data collection.
Lead development of research study documents.
Connaissances
Clinical operations expertise
Project management
Regulatory knowledge
Organizational skills
Attention to detail
Formation
Bachelor’s degree in Life Sciences or related field
Description du poste
A leading health solutions company is seeking a Research Coordinator to support clinical studies, ensuring compliance and efficiency. This role involves managing research protocols, participant interactions, and regulatory documentation. Candidates must hold a bachelor's degree in Life Sciences and have at least 5 years of experience in clinical operations. The position offers competitive compensation and comprehensive benefits, making it an excellent opportunity for those passionate about health and wellness.
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