**Looking for East Coast Candidates**
We have an opportunity with a biopharmaceutical company that is looking for a Clinical Monitoring Lead to join their team on a 6-month contract with a good possibility for conversion or extension!
Qualifications
- 5 years of experience in Oncology required
- Relevant experience of pharmaceutical drug development:
- Experience of minimum 1 year (ideally 2 years) of Lead CRA e.g. coordination of clinical activities/site management activities for the setup and running of international registrational studies (multiple sites/countries).
Responsibilities
- Take responsibility for coordinating the clinical monitoring activities, overseeing the CRO clinical /site management activities, and co-monitoring the assigned international Ph2/3 clinical studies in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and SOPs to the most rigorous standards of quality, timely delivery and within budget, in order to assist in the delivery of Clinical Development objectives and achieve clinical excellence.
- Coordinate the achievement of assigned clinical study deliverables within a matrix organization under the leadership of the Clinical Project Managers (CPM).
Please apply here directly if interested but If you are genuinely not interested, is there someone you can recommend?
