We are looking for an accomplished and driven Medical Affairs Manager - Europe to oversee medical and clinical functions across Europe for a pioneering Class III implantable medical device. This position plays a crucial role in shaping clinical strategies, facilitating medical education, and ensuring adherence to regulatory and quality standards.
About the Role :
As the regional medical authority, you will collaborate with healthcare professionals, clinical teams, and internal stakeholders to support therapy implementation. You will be responsible for supervising clinical studies, delivering specialized training, and refining patient care processes. Furthermore, you will work alongside leadership teams to integrate cutting-edge medical insights into both commercial and clinical initiatives.
Key Responsibilities :
* Oversee clinical research activities, ensuring alignment with regulatory requirements and organizational goals.
* Develop and execute training programs for healthcare providers, including physicians and multidisciplinary teams.
* Maintain medical documentation and ensure strict compliance with quality system protocols.
* Monitor and evaluate implant procedures across Europe to enhance patient outcomes.
* Serve as a key medical representative, engaging with leading experts, advisory boards, and healthcare institutions.
* Conduct internal training sessions and virtual seminars to support business and clinical objectives.
* Stay informed on evolving clinical research to guide advancements in therapy applications.
* Act as a liaison with global headquarters to ensure European medical affairs strategies align with broader corporate initiatives.
* Contribute to market expansion efforts by promoting awareness and acceptance of the therapy.
Qualifications :
* PhD in Medicine (preferred) or a relevant degree in biomedical sciences or a related field.
* Significant experience in medical affairs within the medical device sector, particularly involving Class III implantable devices.
* Strong background in clinical research, medical documentation, and regulatory compliance.
* Demonstrated expertise in training and educating healthcare professionals.
* Excellent communication and teamwork capabilities to coordinate cross-functional initiatives.
* Willingness to travel across Europe as required.
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