Job Description

The Life Science Career Network
CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.
Our client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a world-leading pipeline in Neuroscience and Dermatology with one of the strongest pipelines of Phase II/III studies in the world.
We are currently looking for a:
Director Real World & Innovative Evidence
on a 1 year-contract, with possibilities of extension, based in Basel, Switzerland.
In this role, you will be responsible for creating and executing evidence strategies that provide scientifically robust real-world evidence (RWE) to support product development, market access, and healthcare decisions.
Main Responsibilities:

• Develop and implement integrated evidence strategies in collaboration with internal stakeholders to ensure robust value demonstration of our medicines.
• Serve as a thought leader and change agent, driving the creation and execution of Global RWE/Integrated Evidence strategies.
• Design and deliver scientifically rigorous evidence solutions tailored to corporate priorities, impacting patient outcomes and societal benefit.
• Build strong partnerships with Medical Societies, Academic Institutes, payer bodies, and data owners to advance RWD research collaborations.
• Lead innovative data and analytic platforms, ensuring cross-functional and cross-geographical best practice sharing.
• Collaborate with key markets to provide timely, actionable evidence supporting product access, reimbursement, medical education, and patient advocacy.

Qualifications and Experience:

• Relevant working/residency permit or Swiss/EU-Citizenship required.
• At least 7 years in biopharma, academia, healthcare provider/payer, or consultancy with deep RWD/RWE expertise.
• Proven track record in delivering impactful evidence for regulatory approval, market access, and clinical adoption.
• Experience leading cross-functional teams and collaborating with Clinical, Commercial, Market Access, and Regulatory functions.
• Expertise in research methodology, statistical methods, and epidemiological research.
• Excellent communication, leadership, and strategic thinking skills.

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us.