Coordinates and manages the department/center’s research portfolio, maintaining working knowledge of projects, grant budgets, and IRB protocols
Job Summary
Coordinates and manages the department/center’s research portfolio, maintaining working knowledge of projects, grant budgets, and IRB protocols.
Responsible for administrative management, organization of, and participation in program meetings, scientific meetings, and CME programs.
Provides monitoring, review, and tracking of clinical data, preparation of study specific documents according to FDA regulations, and QA process implementation.
Matching Summary
Coordinates and manages the department/center’s research portfolio, maintaining working knowledge of projects, grant budgets, and IRB protocols.
Skills & Requirements
Must-have
regulatory experience
manage research portfolio
coordinate subcontracts
manage program funds
develop IRB protocols
track project timelines and budgets
manage IRB process
Nice-to-have
demonstrated leadership skills
strong organizational skills
exceptional interpersonal skills
self-directed and results driven
ability to work independently and as part of a team
Key Requirements
Bachelor’s degree preferred or Associate degree
Two years clinical research experience or project management experience