Sweden_Senior Medical Advisor

Om jobbet

Celltrion Group provides biosimilar and innovative biopharmaceutical medications to help increase patient access to advanced therapies around the world.

Celltrion Group offers biologics to about 110 countries, along with more than 30 global partners around the world. With hands-on experience and knowledge accumulated through years of working in the advanced pharmaceutical markets around the world, Celltrion Group has been securing distribution channels and providing patients with biosimilars at affordable prices.

About the Role

We are looking for a Senior Medical Advisor to our Swedish team. Working in partnership with the Nordic Medical team the Senior Medical Advisor will build partnerships with external medical experts to communicate evidence based scientific, technical and development matters primarily within Sweden.

Key Responsibilities:

• Establish and manage scientifically based relationships with clinical investigators, MEs, and other stakeholders in Sweden and Denmark
• Provide scientific and educational information to relevant MEs, speakers & investigators on data as appropriate
• Facilitate and maintain legitimate scientific exchange related to compounds and pipeline with MEs, speakers, and investigators to advance understanding of new scientific principles, research trends, and current scientific debate
• Maintain an accurate understanding of the following aspects of Celltrion Healthcare's biologic products: mechanism of action, production, indications, dosing, clinical studies, efficacy & safety, usage, maintenance of the products
• Providing market and clinical understanding of pipeline therapeutic areas
• Gathers external insights and utilizes insights to shape the product's scientific strategy
• Collaborates with colleagues to gather, analyze and report insights from all legitimate sources that may impact developmental plans, trial designs, launch strategies, current brand strategies and tactics
• Acts as a field-based reference point for non-promotional scientific and clinical expertise to field force and encourage self-sufficiency in the field force where feasible
• Identifies and tracks potential research opportunities that are closely aligned with development objectives through facilitating Clinical Research as agreed
• Responsible for milestone delivery in supported research projects
• Proactively develops scientific research concepts and ideas with investigators that deliver new data to enhance product profile
• Provide study and site level feasibility and research site recommendations
• Provide strategic support during the entire trial process to support study and patient accrual as appropriate, and manage the investigator relationship
• Manage the regulatory life cycle (reviewing/coordinating SmPC text and packaging mock-ups, creating mini SPC, mini text for patients, aRMM submission, FASS, Roda Webben, etc) at local level
• Manage the medical query from customers
• Manage the PV related tasks (safety cases reconciliation as per the SDEA, aRMM distribution, local PV SOP etc)

Background Requirements:

• Masters, PhD or other higher level scientific based qualification (e.g. medic, registered pharmacist etc.)
• Previous experience within Medical Affairs/Medical Advisor/MSL role in the pharmaceutical industry
• Experience in working with the biologic, biosimilar, and/or immunology products
• The ability to understand, process, communicate and present scientific information
• Strong presentation, communication and networking skills
• The ability to work accurately, with attention to detail
• Proven track record of cross-functional team working
• Ability to manage multiple projects and adapt priorities according to business and strategic needs
• Excellent verbal and written communication skills (Swedish, English)

If this job sounds like a fit for you, share us your CV and application by 18.4.2026.