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Medical Affairs Consultant (candidate pool), Belgium
Client: Keyrus Life Science
Location: Belgium
Job Category: Other
EU work permit required: Yes
Job Reference: f6843f84ba84
Job Views: 4
Posted: 26.04.2025
Expiry Date: 10.06.2025
Job Description
Job Description
Keyrus Life Science is frequently seeking Medical Affairs Consultants to join our consulting team for various client projects (ranging from large pharma to small biotech) based in Belgium.
This description illustrates how your potential role could look. Once a specific project and client are identified, you will be informed and have the opportunity to be presented to our client.
Your potential challenges could include:
* Developing and maintaining the highest scientific and medical expertise across different therapeutic fields and related specialties, especially in areas impacting the company.
* Maintaining up-to-date knowledge of local pharmaceutical regulations in collaboration with Regulatory Affairs and ensuring adherence to company policies and procedures.
* Attending national and international meetings and congresses for education, engagement, and scientific exchange.
* Supporting the development and implementation of a local Medical Affairs Plan and strategy to promote best clinical practices and corporate objectives.
* Providing accurate and comprehensive scientific information to decision-makers and healthcare providers.
* Identifying and addressing staff training needs, and providing medical leadership for training programs for commercial and other teams.
* Responding to Medical Information inquiries internally and externally, in line with global resources and local regulations.
* Engaging with Key Opinion Leaders and stakeholders, including professional organizations.
* Supporting the assessment of new indications, patient pathways, diagnostic practices, and management strategies in relevant disease areas.
* Assisting in clinical study feasibility, trial management, and disease registry activities.
* Ensuring publication activities comply with SOPs, including filing, archiving, and communication.
* Updating dissemination plans periodically and maintaining timelines for publication delivery.
* Providing updates on scientific publication activities as required.
* Participating in regulatory document submissions and other medical affairs documentation.
Profile
* Minimum 2 years’ experience in Biotechnology/Pharmaceutical fields.
* Fluent in English; French and/or Dutch are valuable assets in Belgium.
* Prior Medical Affairs experience is essential.
* Proven relationship development skills and ability to present complex scientific data.
* Experience working in matrix organizations or virtual teams is a plus.
* Strong multitasking, project management, and organizational skills.
* Excellent interpersonal, communication, presentation, persuasion, and influence skills.
* Proficiency in MS Office.
What We Offer
Join a growing team in Belgium, serving as a key contact within the Consulting department on Keyrus Life Science projects. Enjoy an active role in a dynamic, international environment with professional colleagues.
We provide comprehensive training and a competitive salary package with attractive benefits (company car, petrol card, vouchers, insurance, etc.) tailored to your experience.
Who We Are
Keyrus Life Science is an international provider of Consulting, CRO, and Functional Services, committed to transparency, integrity, and excellence. Our human-centered approach and high-quality services distinguish us in the industry. We support all stages of drug development, including Project Management, Clinical Operations, Pharmacovigilance, Regulatory Affairs, Data Management, Medical Review, and more.
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