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Job summary
A prestigious educational institution in Boston is seeking a Research Specialist IV to provide on-site clinical oversight and administrative coordination for research studies. The role involves supervising sessions, ensuring participant safety, and managing study logistics. Ideal candidates will hold a doctoral degree and have 3–5 years of clinical research experience. This part-time position offers a varied hourly salary based on experience and responsibilities, emphasizing collaboration with investigators and compliance with regulatory standards.
Qualifications
3–5 years of experience in clinical research or related field.
Responsibilities
Supervise study sessions to ensure participant safety and protocol adherence.
Maintain regulatory and safety compliance with institutional and federal guidelines.
Manage study logistics, including scheduling, equipment setup, and data entry.
Contribute to data analysis, reporting, and preparation of manuscripts and presentations.
Collaborate with investigators and research staff to support study execution and dissemination.
Skills
Clinical oversight
Data analysis
Regulatory compliance
Logistics management
Education
Doctoral degree (PhD, MD, or equivalent)
Job description
A prestigious educational institution in Boston is seeking a Research Specialist IV to provide on-site clinical oversight and administrative coordination for research studies. The role involves supervising sessions, ensuring participant safety, and managing study logistics. Ideal candidates will hold a doctoral degree and have 3–5 years of clinical research experience. This part-time position offers a varied hourly salary based on experience and responsibilities, emphasizing collaboration with investigators and compliance with regulatory standards.