Executive Director, Global Medical Affairs Therape job in San Diego, CA| Recruit Arrow
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Title
Executive Director, Global Medical Affairs Therape
Location : California, San Diego
Refer job # HYRF338231
 
Job Responsibilities and Requirements: RESPONSIBILITIES: Provides expert opinion on the current trends in the pathophysiology, diagnosis, existing and emerging treatment options as well as unmet medical needs in the therapeutic area to inform key medical and business decisions. Build mutually-valuable partnerships within the medical community though the design, planning and execution of the Medical Affairs program. Coordinate Medical Affairs activities across therapeutic area and regions so that activities are consistent, aligned to strategy, and leverage each other. Develop strong relationships with global key opinion leaders, key professional societies, and organizations in collaboration with regional medical affairs and clinical colleagues through scientific dialogue pertinent to Celgene I&I interest. Participate in, support, and develop key global clinical and medical affairs strategies in conjunction with global commercial counterparts. Provide ongoing and interactive technical and medical expertise to execute on these strategies. Actively participate in global strategy development via team meetings. Provide expertise into the phase 3b/4 development programs and lifecycle management activities for Celgene compounds within therapeutic area as well as business development opportunities. Participate in formal scientific review of submitted Investigator Initiated Trials and related medical affairs activities (e.g. registry/database projects, epidemiological surveys etc.). Provide timely and interactive feedback to achieve optimal study designs and to ensure adequate study progress. Provide medical support to country and regional medical affairs organizations, including developing and delivering training curriculum and content. Chair and develop content for advisory meetings with opinion leaders. Develop content for medical symposia. Actively participate on global promotional review committees to ensure content is medically appropriate and compliant with internal and external requirements. QUALIFICATIONS SKILLS: M.D., D.O., or equivalent degree with work experience in the area of neurology. Minimum 8 years of progressive experience in the therapeutic area, preferably in the biotech or pharmaceutical industry or similar academic institution, is required. Excellent written and oral communication skills, including strong formal presentation skills. Excellent planning and organization skills. Strong interpersonal skills commensurate with the need to effectively manage teams of peers and to work closely with both external physicians/scientists and numerous in-house support groups. Ability to maintain the highest degree of confidentiality and integrity, represent the company's high ethics, moral behavior, and professionalism. Demonstrated ability to maintain scientific credibility while being commercially supportive, and to communicate scientific results and effectively respond to data queries from customers and/or consultants. High proficiency in problem solving ability and strong scientific analytical skills. Knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies. Basic knowledge and appropriate application of biostatistics; proficiency using standard software suites. Experience working in an international environment. Ability to travel (frequent travel will be required). Proficient in Microsoft Office applications including PowerPoint and Outlook.
 
Contact the Following Recruit Arrow Office:
Los Angeles
202 S Lake Ave, Unit 250
Pasadena, California 91101
Email: jobs@recruitarrow.com
 
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