Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward!

Proclinical is seeking a Director of RWE & Innovative Evidence to lead the development and implementation of evidence strategies that support healthcare decisions and inform business strategies. This role focuses on leveraging real-world evidence (RWE) and integrated evidence to optimize product development and value demonstration. You will collaborate with cross-functional teams and external stakeholders to drive innovative approaches in evidence generation, ensuring alignment with global and local needs.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Develop and execute integrated evidence strategies to support the value of medicines.
• Act as a thought leader and advocate for RWE and innovative evidence solutions.
• Identify evidence needs and recommend fit-for-purpose data and methodologies.
• Deliver high-quality, scientifically rigorous evidence aligned with corporate priorities.
• Collaborate with internal and external partners to ensure scientific rigor in study design and analysis.
• Build partnerships with medical societies, academic institutions, and other stakeholders for RWD research collaborations.
• Contribute to enterprise-wide initiatives and innovative data platforms to enhance evidence use.
• Work with key countries to develop evidence supporting product value, access, and advocacy.
• Define goals, identify gaps, and establish best practice standards for evidence generation.
• Prioritize funding and resources based on strategic trade-offs and therapeutic area needs.
• Stay updated on emerging trends, technologies, and methodologies in RWE.
• Foster a collaborative and entrepreneurial culture, promoting innovative ideas and solutions.

Key Skills and Requirements:

• Expertise in real-world data (RWD), RWE, and related disciplines for evidence generation.
• Strong understanding of drug development and ability to deliver impactful evidence for regulatory, market access, and clinical adoption.
• Experience with research methodologies, statistical methods, and observational/epidemiological studies.
• Proven track record in leading RWD research projects, including publications.
• Cross-functional experience with clinical development, market access, HEOR, medical, safety, and regulatory teams.
• Strong leadership, communication, and organizational skills.
• Ability to manage change, inspire teams, and implement new strategies effectively.
• Results-oriented with the ability to meet deadlines in a dynamic environment.
• Preferred: Extensive industry experience across drug development stages, prior Novartis experience, and a strong external network in RWE.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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