The Senior Clinical Research Coordinator (CRC) oversees and administers clinical research studies and associated activities
This position will assist with the development and management of study budgets
The Senior CRC will assist with the review of protocol requirements and assist with the collection of impact statements needed to properly assign costs to each assessment/procedure
The Senior CRC shall cooperate as necessary with the Geneva Corporate Manager to ensure that studies remain financially healthy, including but not limited to, the review of monthly budget reports as well as budget forecasts
The Senior CRC assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed
This position may recruit and coordinate research subjects, as appropriate, and serves as principal administrative liaison for the project

Bachelors degree or equivalent work experience required; masters degree preferred
8 years’ experience in clinical research preferred
5+ years non-profit, research, or healthcare experience desired
Certified Clinical Research Coordinator (CCRC) certification preferred
Demonstrated competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines

Senior Clinical Research Coordinator

Key skills