Clinical Medical Affairs IIIPosted: November 8, 2009
Clinical Medical Affairs III
Responsible for strategy, development, management and implementation of clinical trials. Develops and networks with key opinion leaders and customers to develop and implement clinical trials, participate in investigator selections, organization of investigator meetings, and writing of protocol documents for regulatory submissions. Develops budgets, schedules, and performance standards for self and project. Develops and implements publications and communication plans arising from phase IV studies. Manages all other medical marketing initiatives. Provides medical support and input to marketing teams regarding product. Opportunity to provide strategic input into global clinical development plans. Requires 8+ years experience.
Physician will work with the IM Group and will be assigned to specific projects. Will be expected to provide support to the clinical team as directed by the clinical leader. This support will include, but may not be limited to, the following services: preparation of regulatory documents and responses, protocol writing, review of clinical data, medical review of newly received and updated CIOMS reports from DSS on a monthly basis, data safety monitoring, CRF review, report writing and review and delivery of manuscript publications.
Would prefer an MD with at least 8-10 years of pharmaceutical industry experience.
Client is interested in having strong clinical research background and significant experience working on new drug applications.
Location: RARITAN, NJ
Duration: 06 months
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