Candidate will develop and direct the Clinical Pharmacology Program in an environment of rapid growth. Roles include protocol development as consultant to Sponsors, clinical/safety oversight of ongoing studies, on-site management of study operations in conjunction with the director of site operations and administration of IRB related processes.
Candidate will coordinate activities with operational, regulatory, project management, data management and QA groups within Clinilabs, and should therefore be an effective communicator, team member and leader. Candidate will also participate with Business Development activities and responses to RFPs.
Requirements:
- M.D. (board certified) with post graduate training in clinical pharmacology
- Licensed in the State of New York
- Familiar with/trained in GCP, HIPAA and 21CFR part 11 compliance
- Knowledge of pharmacokinetic and pharmacodynamic principles
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