What we will accomplish together: Alsinova is looking on a regular basis for Medical Affairs Consultants to join our consulting team for clients' projects (from big pharma to small biotech) based in Belgium. 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.

You:

• Relevant scientific degree essential (MD, PhD or PharmaD).
• Minimum 2 years Biotechnology / Pharmaceutical field experience.
• Proven track record of relationship development in the industry.
• Prior exposure to complex matrix organizations or experience working as part of a virtual team is a plus.
• Demonstrable multitasking, project management, and execution skills.
• Proficiency with computer skills, such as MS Office.

Our Benefits Joining Astek means choosing:

• an experience accelerator, where every assignment is an opportunity to progress
• access to a multitude of technically exciting projects for our clients as well as internally
• individualized, local support for a tailored career path
• continuous learning, thanks to our internal training academy
• a friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practices Let's move forward.