Associate Director, Global Clinical Trial Manager

Work Your Magic with us! Start your next chapter and join EMD Electronics.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers.

Location:

The Associate Director, Global Clinical Trial Manager is a hybrid position (3 days onsite, 2 days remote) located in the Boston area (Billerica). There will be minimal travel, possibly domestic and international, to meet business needs.

Your Role:

Reporting to the Head of Compound Operational Leads, the Global Clinical Team Manager (GCTM) has a key organizational role in supporting the Global Clinical Lead (GCL) by facilitating the management and delivery of cross-functional Clinical Team (CT) efforts.

The GCTM partners with the GCL to support activities that ensure the seamless translation of strategic elements of the Integrated Evidence Plan (IEP) into actionable clinical strategies and Clinical Development Plans. The role requires close collaboration with various functional sub-teams to ensure the delivery and integration of their functional plans (e.g. Biomarker Plan, Clinical Pharmacology Plan).

GCTMs serve as the operational enablers of the CT — ensuring that cross-functional plans are integrated, governance interactions are well-prepared and outcomes are clearly communicated, and any risk to program timelines are addressed through CT discussion and management. By maintaining accuracy of program timelines, budgets, and risk registers, this role directly protects the integrity of clinical development plans and enables faster, better-informed decisions at governance level.