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Senior Clinical Manager

Location: Northeast

Prepare clinical protocols and oversee
development of case report forms.

Develop investigational site study budgets and spearhead contract negotiations with sites.

Monitor clinical trial investigative sites and/or direct activities of vendors (CROs) tasked with monitoring clinical trial sites in accordance with GCPs and company SOPs.

Interact with study coordinators and other
related site personnel.

Participate in the preparation of clinical databases
and final clinical trial reports.

Monitor of central laboratories and other contractors.

Supervise, as needed, clinical study managers in developing of protocols, case report forms
and monitoring plans.

Qualifications:

4 years minimum experience in clinical research
in a pharmaceutical company.

Available for 20-30% travel

Superior organizational and interpersonal skills