Senior Safety Manager

As a Senior Safety Manager at LINK Medical, you will play a central role in delivering high\-quality pharmacovigilance services to our clients and ensuring compliance with global regulatory requirements.

Key responsibilities

• Focus on pre\-marketing safety activities within clinical development projects, but may also undertake postmarketing tasks as required


• Provide safety expertise in client projects, tailored to your experience and role


• Manage and deliver delegated projects efficiently, on time, and within budget


• Perform operational PV activities, including SAE handling, SUSAR reporting, and periodic safety reporting


• Contribute to Safety Management Plans and other key safety deliverables


• Participate in clinical trial teams and provide input to clinical development and safety strategy


• Advise clients and colleagues on safety\-related matters


• Develop training materials and deliver internal and external training


• Act as an active member of the Safety SME group, contributing to procedures and best practices


• Collaborate closely with colleagues across LINK Medical, both locally and internationally


• Contribute to the development of LINK Medical’s safety service offerings

• Degree (MSc or BSc) in Pharmacy, Life Sciences, or a related natural/health science discipline


• Minimum 5 years of experience in clinical safety/pharmacovigilance


• Solid theoretical and hands\-on knowledge of clinical trial safety, including applicable regulatory requirements


• Experience working in a CRO or other service\-oriented environment is an advantage


• Fluency in English and at least one Scandinavian language


• Strong general IT skills and proficiency in standard office tools


• Experience with safety databases (e.g. HALOPV) is considered an advantage

• Proactive and self\-driven, with the ability to take initiative and work independently


• Demonstrates accountability and takes ownership of actions and deliverables


• Detail\-oriented with a strong focus on quality and accuracy


• Committed to continuous professional development and expanding expertise


• Actively shares knowledge and contributes to team learning


• Collaborative team player who builds trust, motivates others, and fosters a positive team spirit


• Business\-minded with the ability to identify and contribute to new opportunities


• Delivers high\-quality work with professionalism and maintains a respectful and service\-oriented approach toward clients and colleagues

We offer an exciting and challenging position in a European CRO and Regulatory Service Provider that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given engaging assignments requiring efficient collaboration with industry partners, clinical and scientific teams and the regulatory authorities, and you will have the opportunity to further develop your competencies in different areas according to your aspirations and the customer’s and LINK Medical needs. We offer a competitive compensation and benefit scheme for all employees.

Contact information

If you would like to know more or have any questions about the position, please contact Berit Nautrup Andersen, Safety Director (berit.nautrup.andersen@linkmedical.eu). All applications are treated confidentially.

Last day for submitting your application: 08\-Aug\-2026.

Applications will be reviewed on an ongoing basis.

Dette opslag er fra indeed. Se originalopslag ↗