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
Desired qualifications
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
Personal characteristics
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
LINK Medical offers
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.