Medical Expert - Clinical Science (all genders)

Headquarter - Wedel: 06.11.2026
Medical Expert - Clinical Science (all genders)
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About medac

We are a strong community: with more than 2,000 employees worldwide, we are committed to improving human health. Our work is more than just a job. With a career at medac, you can make a real difference in the industry. Look into this job opportunity and become part of an exceptional workforce.

About the Role


Hands-on Medical Expert responsible for clinical-scientific and regulatory activities across the product lifecycle, with a strong focus on the preparation of high-quality regulatory documentation, scientific data interpretation, support of global submissions and lifecycle management activities.

Acts as a cross-functional scientific partner, translating clinical and scientific data into clear medical and regulatory conclusions. Contributes to benefit-risk assessments, evidence-based decision-making and health authority interactions in close collaboration with Clinical Development, Regulatory Affairs and Pharmacovigilance.

Supports clinical trials through medical monitoring activities and serves as a medical advisor to Clinical Development teams.

Provides medical-scientific oversight of Managed Access Programs (MAP) and Named Patient Use (NPU) requests, including medical assessment of individual requests and benefit-risk evaluations to support approval decisions.

Participates in scientific evaluations and due diligence activities for new product opportunities, including assessment of clinical data, unmet medical need and benefit-risk profiles.

Key Responsibilities


  • Author, review and lead high-quality clinical and regulatory documents (CTD), including Clinical Overviews & Clinical Summaries, Clinical Expert Statements, Risk Management Plans (RMPs), SmPCs, CCDS, PILs, PSURs/DSURs and other lifecycle management documents
  • Interpret and integrate clinical and scientific data into robust medical-scientific and regulatory positions
  • Ensure medical and scientific consistency, quality and compliance across submission and lifecycle documentation
  • Support benefit-risk evaluations and medical-scientific assessments across the product portfolio
  • Evaluate Managed Access Program (MAP), Named Patient Use (NPU) requests and provide evidence-based medical recommendations to support approval decisions
  • Provide medical monitoring support for assigned clinical trials
  • Serve as a medical advisor to Clinical Development teams, contribute medical expertise to clinical development documents and activities
  • Support clinical development programs through scientific input into study design, development plans and evidence-generation activities
  • Participate in scientific evaluations and due diligence activities for new product opportunities, including assessment of clinical data, unmet medical need and benefit-risk profiles

Your Profile


  • Medical Doctor
  • Several years of experience in Clinical Development, Clinical Science, Medical Affairs, Medical Monitoring, Regulatory Affairs or a comparable role within the pharmaceutical industry
  • Strong scientific writing and communication skills, including experience in authoring CTD Module 2.5 and 2.7 documents
  • Experience with benefit-risk assessments and regulatory interactions
  • Solid understanding of global drug development, clinical research, regulatory requirements and lifecycle management
  • Experience as Medical Monitor and/or scientific support of clinical trials is desirable
  • Experience in the scientific evaluation of licensing opportunities and/or due diligence activities is preferred
  • Ability to provide medical guidance and translate complex scientific information into clear and actionable recommendations
  • Proactive, collaborative and hands-on working style with strong cross-functional communication skills
  • Fluent in English; German is an advantage



Our employees are our greatest asset. And to show our appreciation, we offer attractive benefits: 


  • Your work-life balance is important to us. We offer flexible working hours with the option of working a proportion of those hours remotely, 30 annual vacation days and an excellent cafeteria  
  • Attractive salaries and success-based bonuses for all medac employees 
  • Individual training opportunities: Our medac academy offers a wide range of programmes including leadership training, coaching essentials and language classes 
  • A funded pension scheme and other social benefits 
  • We care for our employees beyond the workplace and provide advice on caring for elderly relatives as well as offering counselling
  • We promote sports and activities to improve our employees’ health 

Are you looking for a new professional challenge and a job with a meaning?

We are a strong community of exceptional people from different countries, with diverse backgrounds, strengths and talents, united by our deep motivation to make a difference in healthcare. As an employer, it is our firm belief that by connecting, we can achieve more. And we are dedicated to providing an environment in which each and every member of our community feels valued and has equal opportunities for success and growth – regardless of where they come from, what they think or what they believe. At medac, we are committed to diversity, equality and inclusion in the workplace.

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