Associate Director (m / f / d) Site Engagement

Locations : Germany, Poland, Netherlands, Croatia, or Spain

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

Your Role & Responsibilities as Manager

In this position, you will be responsible for ensuring the successful execution of Teva’s Site Relationship Management strategy. Working closely with Clinical Trial Liaisons (CTLs) and key business stakeholders, you will position Teva as the Sponsor of Choice for clinical trial sites. You will lead and support the development of strategic relationships with clinical sites, Contract Research Organizations (CROs), Medical Affairs, and other internal functions to establish a best-in-class site engagement model.

Your role will require you to effectively collaborate with a wide range of internal and external partners to address site-level challenges, ensure optimal study performance, and enhance recruitment efforts. You will also be responsible for coaching CTLs to act as true partners and representatives of Teva. You will work with cross-functional teams to resolve issues, share insights, and support continuous process improvements that align with Teva’s clinical goals.

Key Responsibilities

• Lead training, mentoring, and oversight of Clinical Trial Liaisons (CTLs).
• Ensure the execution of strategic partnership models and frameworks to be implemented across key clinical trial sites.
• Strengthen relationships with clinical sites through collaboration with CTLs, identifying performance challenges, and optimizing site engagement to become the Sponsor of Choice.
• Work alongside Medical Science Liaisons (MSLs) and clinical / medical colleagues to support site relationships and identify new clinical sites.
• Collaborate with the CTL group and broader Global Clinical Operations (GCO) team to address study-level challenges and resolve issues in a timely manner.
• Escalate unresolved study or site issues to the manager.
• Share insights, successes, and challenges from sites with management to support process optimization, mitigation, and future planning.
• Regularly report on site performance status and track engagement and enrollment metrics.
• Identify opportunities to enhance and support site-level recruitment efforts.
• Stay informed about market activities, trends, and regulatory changes affecting clinical recruitment and improve Teva’s clinical recruitment strategy.
• Demonstrate a deep understanding of clinical sites, site networks, and the competitive clinical trial landscape.
• Assist in deploying and executing site engagement strategies, tactics, and processes.
• Coach CTLs to embody Teva’s values and serve as effective partners with clinical sites.

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At Teva

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Research & Development