Medical Manager

hace 2 semanas

Ciudad de México Pfizer A tiempo completo

MEDICAL:
- Provides support and the necessary medical and scientific information of Pfizer Biopharmaceutical Group products to internal and external customers assuring compliance with Corporate and Local Procedures and applicable regulations providing full support to our local medical objectives.- Collaborates with Drug Safety Unit, Global/Regional Therapeutic Areas and Regulatory Affairs in preparation of the Risk Management Plan of the products under her/his responsibility.- Collaborates with Regulatory Affairs to review and assess the Local Language Document of the products under his/her responsibility- Management of the whole process of the Clinical and Research Collaborations and Local and Regional Non
- Interventional / Interventional Studies (different from BE studies) as per the applicable Pfizer processes, and to the therapeutic area under his/her responsibility following major milestones and budget.- Provide guidance with regards to do´s and don’ts to commercial colleagues, be role model with regards to Compliance.- Be the official spoke person with MD for their portfolio of products to healthcare authorities.- Manage and coach MSLs and/or other direct reports (if any).- Develop and maintain professional relationships with KOLs, Medical Societies and academic centers to be partners in CME projects- Manage Medical Affairs annual budget as planned.- Develop the Medical Affairs annual local plan, aligned to brand objective(s), and coordinate derived tactics.- Assure Medical Affairs plan execution with the collaboration of the MSL

CLINICAL RESEARCH- Together with the cross functional team identify and discuss the scientific question and determine the need to conduct locally sponsored clinical trials
- _e.g.,_ phase IV clinical trials, epidemiological, Pharmacoeconomics etc.) to support the strategies of the assigned Pfizer products.- Responsible of the locally sponsored clinical trials, proposing investigators, site identification, coordinates investigators´ meeting and once the clinical trial is ongoing will continue to have direct contact with investigators and the medical overview of the trial.- Management of the whole process of the Clinical and Research Collaborations and Local /Regional Non
- Interventional / Interventional Studies (different from BE studies) and compassionate access programs until their completion to assure adherence to Pfizer requirements and local regulations.- Collaborates with Drug Safety Unit, Global/Regional Therapeutic Areas and Regulatory Affairs in preparation of the Risk Management Plan along with the conduct of all Post Authorization Safety Studies (PASS) conducted as a result of a commitment to the MoH as a condition of marketing approval.- Lead the publication strategies of local clinical and epidemiological trials in adherence to the Pfizer requirements.- Participate before, during, and after audits and inspections when required and during the implementation of the Corrective Action/Preventive Action (CAPA) of the clinical studies under his or her responsibility.

MARKETING- Full involvement to provide scientific and medical inputs during the setup of new products, working together with Business Analytics and Insights area.- Collaborates during product launch process, including his/her participation in Strategic Planning/New Product meetings.- Collaborates with CBL/CPL in designing marketing campaigns. Provides medical and scientific knowledge during the development of Promotional Materials and/or activities of Pfizer products for the assigned therapeutic area.- Reviews and validates scientific contents of the activities sponsored by Marketing and Customer Engagement Programs together with the CBL/CPL.- Maintains close communication with Medical Associations, Ministry of Health and Academic Institutions for projects regarding Medical and Marketing Areas, including Continuous Medical Education Programs.- Develops with Key Opinion Leaders material for scientific presentations of the products entrusted.- Collaborate in the trainings of their portfolio of products under their responsibility.- Coordinates Medical aspects of scientific events (educational and/or promotional), selecting speakers and assuring ethics and scientific content (Communication management to Sales Force, Media, and Opinion Leaders) for Continuous Medical Education Programs.- Train the trainers and to their commercial colleagues on product and disease knowledge of their portfolio of products. Validate training materials.- Maintains close communication with Regional Team members of Pfizer products for the assigned therapeutic area, actively participating in teleconferences and in the annual meetings MM/PP (Medical Managers/Product Physician meeting).- Provides input, feedback, and collaborates in Market Research activities as needed.- Provides medical and scientific support to Corporate Affairs area in relation to public dissemination of Pfizer products for the assigned therapeutic area.- Acti

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