Job Description

Responsibilities

• Provide clinical oversight and medical expertise throughout the conduct of clinical trials.
• Contribute medical insight to study-related documents, including reports, regulatory submissions, and manuscripts.
• Address and manage safety concerns in clinical studies, collaborating with team members to evaluate trial-related risks and issues.
• Support business development efforts by participating in proposals and meetings with potential sponsors as needed.
• Work cross-functionally with other departments to support all phases of clinical studies, including feasibility evaluations, protocol design, training initiatives, medical information management, and review of medical documents.
• Ensure strict adherence to research protocols and lead others in compliance with organizational and regulatory standards.

Qualifications

• Medical Degree (M.D.) with specialization in Gastroenterology required
• Eligibility for medical licensure is mandatory
• Board certification is preferred
• Experience in clinical trial research is strongly preferred
• Previous involvement in pharmaceutical-sponsored clinical research is an advantage
• Willingness to travel up to 20%

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