Clinigen

Global pharmaceutical services and medicine access

Medical Affairs Lead

Biology & BiotechConfirmed live in the last 24 hours

Full-timeRemote in GermanyRemote

About the Job

Requirements

A bachelor's degree or higher in a scientific discipline such as medicine, pharmacy, or life sciences, or a related field.
Strong knowledge of therapeutic areas relevant to the company, including haematology and oncology.
Strong communication and presentation skills.
Ability to build and maintain relationships with key opinion leaders.
Understanding of regulatory requirements and guidelines related to medical affairs activities.

Responsibilities

Identify, engage, and build strong relationships with key opinion leaders in the medical community.
Collaborate with key opinion leaders to gather insights and feedback and ensure their understanding of the company's products and therapeutic areas.
Maintain regular customer contact through one-to-one meetings, electronic platforms, group meetings, scientific meetings, and symposia as necessary.
Represent the company to health authorities and medical professionals as required.
Participate in medical scientific meetings, training, and scientific advisory boards as required.
Conduct educational programs for healthcare professionals, including physicians, nurses, and other relevant stakeholders.
Provide training on product knowledge, clinical data, and relevant scientific information.
Serve as a scientific resource for internal teams on medical and clinical aspects of company and partner products.
Stay informed about developments in medical science and relevant therapeutic areas.
Align product strategy with best clinical practice and guidelines.
Understand and describe patient journeys in key hospitals, highlighting drivers and barriers to achieving company goals.
Collaborate with clinical operations teams to support clinical trial planning and execution.
Provide input into study protocols, investigator brochures, and other clinical documents.
Ensure accurate and ethical dissemination of medical information to healthcare professionals.
Respond to medical inquiries in compliance with regulatory guidelines.
Lead planning and development of the product medical plan.
Contribute to product strategy formulation and lifecycle development.
Develop and communicate current, factually based scientific and medical content to support the safe and correct use of company and partner products.
Ensure product communications are compliant, factually supported, and aligned with local guidelines.
Collaborate with Medical Information on material and communication sign-off procedures.
Develop, maintain, and deliver training materials for assigned products or therapy areas to relevant internal and external staff.
Support and lead product team meetings as necessary.
Work with marketing, regulatory affairs, and sales to integrate medical strategies into broader business plans.
Participate in internal meetings to share medical insights and contribute to strategic discussions.
Collaborate with other business units to provide medical support and insights as needed.
Contribute to cross-functional initiatives aligned with overall business goals.
Coordinate with internal stakeholders, commercial teams, and market access to engage key institutions and healthcare professionals.
Support business development teams in screening opportunities and collecting information from key opinion leaders.

Medical Affairs Lead

Clinigen · Germany (Remote) · Full-time · Posted 2026-02-23

Workplace: remote

Department: EU, US & ROW

Description

Role Description

In this role, you will be responsible for establishing and maintaining strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the medical community. You will play a pivotal role in supporting the company's medical strategy and ensuring the accurate and ethical dissemination of medical information.

This function will be key in supporting the Head of Medical Affairs in the growth of the Medical Affairs function and support the development of the companies scientific standing, they will therefore operate in both a strategic and operational capacity.

Key Responsibilities:

KOL Engagement

Identify, engage, and build strong relationships with key opinion leaders in the medical community.
Collaborate with KOLs to gather insights, feedback, and ensure their understanding of the company's products and therapeutic areas.
Ensure regular customer contact throughout one to one meetings, electronic platform, group meeting, scientific meetings and symposia as neccessary.
Represent Company to health authorities and medical professionals as and when required.
Active participation in medical scientific meetings, training and scientific advisory boards as required.

Medical Education

Conduct educational programs for healthcare professionals, including physicians, nurses, and other relevant stakeholders.
Provide training on product knowledge, clinical data, and relevant scientific information.
Serve as a scientific resource for internal teams, providing expertise on medical and clinical aspects of the company/partner's products.

Scientific Support

Stay abreast of the latest developments in medical science and therapeutic areas relevant to the company/partners.
Align product strategy with best clinical practice and guidelines.
Understand and describe patient journey in the key hospitals highlighting the key drivers and barriers to achieve Clinigen goals.

Clinical Trials Support and Medical Information Dissemination

Collaborate with clinical operations teams to support the planning and execution of clinical trials.
Provide input into study protocols, investigator brochures, and other clinical documents.
Ensure accurate and ethical dissemination of medical information to healthcare professionals.
Respond to medical inquiries and provide information in compliance with regulatory guidelines.
Lead the planning and development for the Product medical plan
Contribute to the formulation of product strategy and life cycle development
Develop content and communicate up to date and factually based scientific/medical communication messaging and content to ensure the safe and correct use of Clinigen/partners products
Ensure all product communications remain compliant, can be factually supported and aligned with local guidelines at all times.
In collaboration with Medical Information support the material and communication sign off procedure.
Develop, maintain and deliver training materials for assigned product/therapy area to all relevant internal and external staff members
Support and where necessary lead product team meetings

Cross-functional Collaboration

Work closely with cross-functional teams, including marketing, regulatory affairs, and sales, to integrate medical strategies into broader business plans.
Participate in internal meetings to share medical insights and contribute to strategic discussions.
Collaborate with other Business Units to provide medical support and insights as needed.
Contribute to the development and execution of cross-functional initiatives that align with the overall business goals.
Collaborate and align effort with internal stakeholders to engage with key institutions/HCPs including partnership with commercial and market access when needed
Support BD teams in screening opportunities and collecting information from KOLs

Requirements

· Bachelor’s degree or higher in a scientific discipline (medicine, pharmacy, life sciences, or related field).

· Strong knowledge of therapeutic areas relevant to the company, haematology, oncology.

· Excellent communication and presentation skills.

· Ability to build and maintain relationships with key opinion leaders.

· Understanding of regulatory requirements and guidelines related to medical affairs activities.

Benefits

Competitive salary
Discretionary Bonus
Annual salary review
Recognition scheme & employee of the year awards

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Apply at Clinigen

About the Company

Clinigen

Global pharmaceutical services and medicine access

Clinigen provides pharmaceutical services and medicines to help patients gain ethical access to treatments. It revives niche, hospital-only medicines and offers end-to-end services across the product lifecycle, including clinical trial supply, access programs, and global commercialization. Its three divisions—Clinical Services, Access and Commercialisation, and Lifecycle Services—work with pharma partners to manage regulatory affairs, pharmacovigilance, and market access across more than 100 countries for major pharma clients. The goal is to combine product revitalization with comprehensive lifecycle management to improve patient access worldwide.

Company size: 501-1,000
Company stage: IPO
Headquarters: Branston, United Kingdom
Founded: 2010

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