Senior Monitoring Liaison Associate - Basel

Responsibilities: -Coordinate all CRAs assigned to the study -First point of contact for all CRAs, help to address study specific questions -Review and feedback on monitoring related costs proposals -Author Monitoring Plan and Monitoring Logistic Sheet -Review of all visitor reports (SSV, SIV, MVR, COV) for assigned studies and sign off on behalf of CTL -Participate in CTT meetings/TCs on behalf of the CRAs and pass along CRA information. -Assume local trial leader responsibility -Assist in efficient management of monitoring related activities Requirements: - 6 years experience in clinical research - 3 years experience as CRA. ideally experience as LCRA or similar Role - Excellent GCP, ICH knowledge - Novartis SOP knowledge preferable - Medical Knowledge preferable - Bachelor`s degree in science or nursing is desirable - Fluent English (written and oral) For more information about this role or jobs within related specialist areas please send me your CV with your hourly rate expectation for immediate consideration. You can reach me on 0041 44 588 2600 Keywords: Senior Monitoring Liaison Associate, Sr (MLA), CRAs, CROs, Monitoring Plan, Monitoring Logistic Sheet, EDC Training, SSV, SIV, MVR, COV, Freelance, Switzerland, English, SSW/Contract

To find out more about Real please visit www.realstaffing.com [1]

Links:
------

[1] http://www.realstaffing.com