We have an opportunity for a full time, permanent Senior CRA for an established company who are growing. If you only want contract, this is not the right role for you. Candidates MUST have medical device experience which includes 5-7+ years’ experience with on-site monitoring who know how to blend clinical study experience and knowledge with exceptional communication and interpersonal skills. Travel will be 50-60%. And no, that isn’t ‘code’ for 80% travel! This company is dedicated to conducting quality clinical research and not burn out their people. They are not looking for ‘big company, check the box’ type of clinical professionals.
Responsibilities include, but not limited to:
- Conducting pre-study, initiation, routine (as needed to ensure protocol compliance), and close-out visits.
- Training study coordinators/investigators on protocol including study procedures, CRF completion, enrollment, and informed consent.
- Working with staff at study sites to resolve data discrepancies; obtaining/reviewing/processing of regulatory and administrative documents from investigative sites.
- Maintaining investigational product accountability.
- Monitoring IRB requirements.
- Reporting findings from visits.