Medical Director – Gastroenterology/Hepatology

Medical Director – Gastroenterology/Hepatology Overview

• The Medical Director – Gastroenterology/Hepatology will provide strategic leadership for clinical trials and therapeutic advancements.
• Collaborate with multidisciplinary teams to ensure the successful planning and execution of clinical research projects.
• Act as the internal medical expert, interpreting results and contributing to clinical study reports.
• Engage in the development of new clinical projects, including study design and protocol creation.
• Participate in proposal and sponsor meetings to support business development initiatives.
• Hybrid work flexibility is available, with potential for fully remote arrangements based on experience.
• Join a collaborative environment focused on advancing global healthcare through clinical research excellence.
• Contribute to a purpose-driven organization committed to improving patient outcomes worldwide.

Medical Director – Gastroenterology/Hepatology Key Responsibilities & Duties

• Provide medical management and expertise for clinical trials, ensuring adherence to protocols and regulations.
• Contribute medical insights to study reports, regulatory documents, and scientific manuscripts.
• Manage safety issues in clinical trials, collaborating with teams for evaluation and resolution.
• Coordinate feasibility assessments, design processes, and educational efforts across departments.
• Review and edit medical documents to ensure accuracy and compliance with standards.
• Lead protocol adherence and guide teams in strict compliance with research policies.
• Support business development through active participation in sponsor engagements.
• Travel up to 20% for project-related activities and sponsor meetings.

Medical Director – Gastroenterology/Hepatology Job Requirements

• Doctor of Medicine (MD) with specialization in Gastroenterology or Hepatology.
• Eligibility to obtain a medical license; board certification preferred.
• Minimum of 2 years of experience; 5 years preferred in clinical research or pharmaceutical-related roles.
• Prior experience in clinical trial research and safety management is highly desirable.
• Strong knowledge of clinical trial protocols, regulatory requirements, and medical documentation.
• Ability to work in a hybrid environment with occasional travel requirements.
• Excellent communication and leadership skills to guide multidisciplinary teams.
• Proficiency in medical and scientific analysis, with a focus on therapeutic advancements.