Clinical Project Manager
LINK Medical is a trusted Nordic CRO and regulatory service provider, supporting Biotech, Pharma, and MedTech companies with tailored solutions and full-service expertise.
This permanent position is open at our offices in Sweden, Norway, Denmark and Germany
LINK Medical is searching for a Senior Clinical Project Manager (CPM) in one of our offices in Stockholm, Uppsala, Lund, Oslo, Copenhagen or Berlin. As a CPM you will be part of new and innovative projects at LINK Medical. This position is one of the most demanding, challenging, and exciting ones in our company. It takes a special talent to be a successful CPM. You must have very good knowledge of clinical trials, and how to obtain high quality deliverables within timelines and budget. You find inspiration in motivating your project team, and in building and maintaining relationships of trust and confidence with our customers. You keep calm during stressful situations and show patience and endurance while driving your projects forward. We offer an international environment and a unique LINK team of highly specialized and talented colleagues who work together to creatively solve challenges and deliver high-quality results. We offer a competitive salary, career development, and opportunities to learn and grow.
Responsibilities
Ensure that the projects are delivered with high quality, according to scope, on time, within budget, and in accordance with regulatory requirements
Act as primary point of contact for the customer
Follow up third parties/vendors
Participate and present at bid-defense meetings
Communicate actively with project team and stakeholders
Mentor and coach new/junior PMs
Contribute in developing and reviewing procedures/SOPs
Desired qualifications
Natural science degree at university level
Experience from clinical project management from CRO or pharmaceutical industry
Experience from managing cross-functional teams
Experience from Sponsor Oversight and vendor selection
Experience from clinical trials or research within oncology, ATMP or biologics is desirable but not a requirement
Good knowledge in English, in both speech and writing, is a requirement.
Personal characteristics
Self-driven, able to show initiative and work independently
Lead, manage and be a strong motivator for the project team
Structured, organized, and able to prioritize
Very good cooperative ability to create a good relationship with our customers
LINK Medical offers
We offer an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given meaningful tasks requiring efficient collaboration between industry, clinical and scientific teams and the authorities. We offer a competitive compensation.
Contact information
If you would like to know more or have any questions about the position, please contact Hiring Managers Elin Nilsson, Director Clinical Project Management, elin.nilsson@linkmedical.eu or
Maria Fernström, Sr. Director Clinical Project Management, Early Stage Services, maria.fernstrom@linkmedical.eu
All applications are treated confidentially.
Last day for submitting your application: 2026-04-15
- Department
- Clinical Development
- Role
- Clinical Project Management
- Locations
- København, Berlin, Oslo, Lund, Stockholm, Uppsala
- Remote status
- Hybrid
- Employment type
- Full-time
About LINK Medical
LINK Medical is a Nordic CRO, Drug Development and Regulatory service provider offering an exceptionally wide range of expertise, flexible services, and innovative technologies for the biotech, Medtech and pharmaceutical industries across Northern Europe and beyond. We are much more than an international, full service CRO – we have one of the largest Regulatory teams in the Nordics, linking all stages of your product development, from concept and strategy to beyond marketing approval. Our close network of experts and senior advisors is the link to our proven record of quality services as a trusted partner to lead each product on its unique development journey.