Clinical Research Project Manager

Mass General Brigham•Boston, MA

17h•Onsite

About The Position

Responsible for executing on a daily basis, the procedural, managerial and policy decisions made for the studies. Participates in all decisions made for the studies and identifies modifications of existing policies and procedures. Responsible for budget oversight and participates in grant writing and proposals. This role does not require patient care.

Requirements

Bachelor's Degree in a Related Field of Study required.
3-5 years of Research Related Experience required.
Familiarity with FDA regulations for investigating scheduled drugs in clinical trials.
Strong organizational skills.
Strong Communication skills.
Demonstrated analytical skills.
Effective problem solving skills.
Strong computer skills.

Responsibilities

Responsible for the coordination and implementation of research design process and study protocols at one or multiple sites.
On a daily basis, executes the procedural, managerial, and policy decisions made for the studies.
Helps prepare IND applications for scheduled substances.
Participates in all decisions made for the studies and the formulation of policies and procedures.
Identifies modifications needed and works to implement solutions.
Responsible for the development and oversight of project budgets.
Participates in grant writing and proposals.
Serves as the primary contact for outside vendors utilized to ensure efficient operation of the studies.
Responsible for the oversight of all supplies, equipment and files.