Germany Manager mfd Medical Affairs

• Medical Strategy and Scientific Leadership :

Support and execute the Medical Affairs strategy locally for each therapy area through high-level scientific medical communications and other related medical activities including.

Provide medical and scientific expertise related to local phase IV studies design and deliverables (protocols clinical trials sites publications) and to initial review of local IST proposals.

Collaborate with cross-functional teams including Research and Development Clinical Operations and Commercial teams to ensure seamless integration of medical affairs activities.

• Scientific Communication :

Provide medical and scientific expertise to internal stakeholders external partners and customers on ophthalmology-related matters.

Provide input on / prepare local publications / abstracts / reports / medical reviews and if applicable local medical training materials.

Review and approve medical content to ensure accuracy and compliance.

Establish and maintain strong relationships with KOLs academic institutions and relevant medical societies within the ophthalmology field.

Collaborate with KOLs to gain insights gather feedback and identify opportunities for research collaborations and educational initiatives.

Provides local recommendations for expanding the EAME region pool of advocates speakers advisors speakers etc.

• Medical Education and Training :

Develop and deliver scientific and medical training to internal teams including sales marketing and customer support to ensure accurate and effective communication of product information.

Organize and participate in medical symposia advisory boards and educational events to raise awareness and understanding of ophthalmology products.

• Leadership and Team Management :

Lead and supervise a local Medical Affairs team.

• Function as Information Officer

Ensure that all internally or externally used information material both medical and promotional adhere to German laws (HWG MPG AMG) and adhere to regulatory guidelines and industry standards.

This includes also approval processes of EMEA projects during their implementation in Germany.

Qualifications : Education

• Medical degree (MD) or equivalent (PhD) (mandatory)
• Specialization in ophthalmology preferred (desirable)

Experience

• Substantial experience in the pharmaceutical biotech or medical device industry with a focus on ophthalmology (mandatory)
• In-depth knowledge of ophthalmology therapeutic areas and medical affairs best practices (desirable)

Other qualifications

• Excellent communication presentation and relationship-building skills.
• Familiarity with relevant regulations and guidelines related to medical affairs activities.
• In-depth knowledge of ophthalmology therapeutic areas and medical affairs best practices.
• Flexibility to travel as needed for scientific meetings conferences and KOL engagements.

Additional Information :

Grow your career at Santen

A career at Santen is an opportunity to make a difference. Through our long-term vision outlined in Santen 2030 we are committed to be a Social Innovator addressing the social and economic needs of people with visual impairments. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes education and treatment. At Santen we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.

The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs role requirements and individual qualifications regardless of race color ethnicity national origin / ancestry religion sexual orientation gender gender identity / expression age disability medical condition marital status veteran status or any other characteristic protected by law.

If you require any kind of accommodation during our recruitment process please let the recruiter from our team know.

Remote Work : Employment Type :

Key Skills

Proofreading, Adobe Acrobat, FDA Regulations, Manufacturing & Controls, Biotechnology, Clinical Trials, Research & Development, GLP, cGMP, Product Development, Chemistry, Writing Skills

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