Medical Affairs F - M H/F Astek

Your mission (should you decide to accept it):

Your potential challenges will be various, depending on the clients' priorities. The list below gives you examples of our classic activities.

Your daily activities will be:

• Develop and continuously maintain the highest scientific and medical expertise in different therapeutic fields, and adjacent specialties, especially in areas which affect the company.
• Maintain a high level of knowledge of and appropriately implement current local pharmaceutical regulation in conjunction with Regulatory Affairs and ensure implementation of company policies and procedures.
• Attend appropriate national and international meetings and congresses for personal education and engagement and scientific exchange with the medical and scientific community.
• Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives.
• Ensure that accurate and comprehensive scientific information concerning the products is available to decision makers and healthcare providers
• Work closely with partners to identify and address staff training needs.
• Conduct and provide medical leadership to training programs for the commercial teams and other functions.
• Coordinate the timely and appropriate response to internal and external Medical Information enquiries, utilizing global medical information resources and in line with local regulatory requirements.
• Drive the identification, development, and alignment with Key Opinion Leaders, other important customers and stakeholders, including professional organizations.
• Support the implementation of medical affairs practices to assess new indications, the treating community, patient pathways, diagnostic practices, and management strategies in relevant disease areas.
• In conjunction with clinical operations support clinical study feasibility and effective study implementation and on-going management of company sponsored trials, including disease registries.
• Ensure all publication activities adhere to SOPs, which includes filing, archiving, and timely communications and follow-up with all key stakeholders.
• Ensure update of data dissemination plan at periodic intervals as deemed necessary.
• Maintain timelines and facilitated milestones to ensure timely delivery of publication material to scientific congresses and/or journals.
• Provide updates of scientific publication activities on a regular basis and/or as directed. This may include provision of updates in PowerPoint, word, or other formats.
• Participate in timely submission of regulatory documents or other medical affairs documents as needed.