Principal Consultant Clinical Pharmacology & DMPK

Principal Consultant Clinical Pharmacology & DMPK LINK Medical is a trusted Nordic CRO and regulatory service provider, supporting Biotech, Pharma, and MedTech companies with tailored solutions and full-service expertise. I believe I'm a fit! LINK Medical is searching for a highly motivated Principal Consultant Clinical Pharmacology & DMPK in Stockholm, Uppsala or Lund. In this role, you will work in close collaboration with our local and international clients, being responsible for leading and managing Clinical Pharmacology and DMPK activities throughout the drug development lifecycle—ensuring scientific excellence, regulatory compliance, and efficient project delivery. Responsibilities · Provide expert scientific and regulatory guidance on clinical pharmacology, drug metabolism and pharmacokinetics (DMPK) aspects of drug development programs. · Lead and perform gap analyses and develop comprehensive clinical pharmacology development plans. · Conduct or oversee pharmacokinetic (PK) calculations, modelling, and analyses to support development decisions. · Monitor the implementation of clinical pharmacology and DMPK development plans and ensure timely follow-up. · Support clients in the selection, management, and coordination of activities with Contract Research Organizations (CROs). · Author or oversee the preparation of clinical pharmacology sections in regulatory documents such as IMPDs, NDAs, and MAAs. · Provide strategic input for regulatory interactions and submissions related to clinical pharmacology and DMPK. Desired qualifications · PhD in a relevant scientific field. · 5–10+ years of industry experience in clinical pharmacology and DMPK. · Experience across several drug classes such as small molecules, biologics, peptides, oligonucleotides, ATMPs, and/or vaccines. · Advantageous to have experience of modelling and simulation to support dosage selection, PKPD and/or population pharmacokinetic (popPK). · Experience of using WinNonlin software · Strong understanding of regulatory expectations within the relevant field. · Experience with global regulatory submissions such as IND, IMPD, etc. · Excellent communication and technical writing skills. · Proven project management experience with internal and external partners. · Proficiency in Microsoft Office applications. · Fluent in Swedish and English. Personal Characteristics · Proactive, collaborative, and scientific mindset. · Strong relationship-building and coordination skills. · Focusses on client needs, with strong communication and presentation skills. · Well-organized, able to work both independently and within teams. · Commercial awareness and negotiation ability. 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 in an international environment and values as honest and open communication are essential. You will be given meaningful tasks requiring efficient collaboration between industry, clinical and scientific teams, and the authorities. Besides a great working environment with dedicated and supporting colleagues, we also offer a competitive compensation, benefit scheme and great development opportunities for all employees. Contact Information If you would like to know more or if you have any questions about the position, please contact: Ulrika Andersson, Senior Director Drug Development, +46 76 492 4518, [email protected] All applications are treated confidentially and will be evaluated when received, so please apply as soon as possible. Please submit your application in English. Last day for application: 26 June, 2026. Department Early Stage Services Role Principal Consultant Clinical Pharmacology & DMPK Locations Stockholm, Uppsala, Lund Remote status Hybrid Employment type Full-time FTE 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. Founded in 1995 Co-workers 166+