Supervisor Research Programs - Center for Digestive Health

• Accountable for the supervision of all assigned clinical research personnel. Trains new clinical research staff in department research and administrative procedures, evaluates their performance, encourages and supports their further education, and fosters their personal and professional development. Handles performance problems up to and including termination.
• Organizes and manages clinical trials and other research studies.
• Conducts protocol reviews to assess the feasibility of potential studies. Seeks out new research opportunities. Participates in study site selection activities.
• Prepares and submits regulatory documents to study sponsors and any applicable regulatory agencies.
• Works with study investigators to develop recruitment and screening procedures. Composes recruitment documents such as letters and brochures.
• Composes documents, including informed consent forms and protocol abstracts. Creates other study documents and study management tools. Provides guidance and support to other research team members in this area.
• Maintains study and regulatory documentation.
• Carries out study visit tasks and procedures, arranging required tests and other appointments.
• Manages the distribution of workload and back up support for each research team member. Provides support and guidance to other members of the research team. Mentor research coordinators, nurses, assistants, and other clinical staff and trainees.
• Designs, establishes, and provides training programs for clinical research staff.
• Travels to investigator meetings or protocol specific training.
• Communicates with participants throughout the course of the study.
• Prepares grants for funding department research.
• Performs other duties as required or assigned.

• Bachelor’s degree with 5 years of relevant experience, or the equivalent in education and experience, required.
• Master’s degree and/or 10 years of relevant experience preferred.
• Excellent organizational, writing and office software skills required.

Required Licensure/Certifications

• Certification through the Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) required.

Dartmouth Health is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.