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Senior director, gma study management

Dublin
Novartis Ireland
Manager
Posted: 7h ago
Offer description

Senior Director, GMA Study Management
Novartis Ireland – Locations: Dublin, Ireland / London, UK / Barcelona, Spain. Please only apply if you can work at one of these locations. Novartis does not provide relocation support.
Summary
Step into a high‑impact leadership role where your expertise will shape the future of global medical affairs studies. Drive excellence in study operations, lead a talented team, and collaborate with cross‑functional partners worldwide to deliver innovative, high‑quality studies.
Responsibilities

Lead GMA study operations for assigned therapy area from strategic planning through execution and delivery.
Oversee Study Management Team to ensure timely, high‑quality delivery of studies in the portfolio.
Liaise with stakeholders to plan, consolidate, and forecast budgets and resources at the therapy area level.
Drive prioritisation and provide operational input into early planning and budgeting of studies.
Oversee planning and resourcing of interventional studies in collaboration with Global Clinical Operations and Clinical Development teams.
Deliver non‑interventional studies, research collaborations, and investigator‑initiated trials, managing spend and forecasts.
Represent Study Management operations at Therapy Area Medical Affairs Team meetings.
Serve as single point of contact for high‑level study management activities within assigned therapy area.
Build and maintain external relationships with institutions and key opinion leaders involved in GMA studies.
Foster a culture of empowerment, collaboration, and continuous improvement within the Study Management Team.

Qualifications
Essential for the Role

Master’s degree in a scientific discipline; PhD or Doctor of Pharmacy preferred.
At least 12 years of pharmaceutical industry experience with global development and clinical operations expertise.
Demonstrated ability to lead complex, international, multidisciplinary teams in a matrix environment.
Strong understanding of clinical development activities, trial management, and outsourcing processes.
Proven leadership, strategic thinking, analytical, and organisational skills.
Experience in operational aspects of clinical studies, including planning, execution, and budget management.
Excellent English language skills, both written and verbal.
Strong problem‑solving, negotiation, and conflict‑resolution abilities.

Desirable for the Role

Experience in Cardio, Renal, and Metabolism therapy areas.

Commitment to Diversity & Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Why Novartis
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other to achieve breakthroughs that change patients’ lives.
Benefits and Rewards
Learn about the many ways Novartis supports you personally and professionally in our handbook.
Details

Seniority level: Director
Employment type: Full‑time
Job function: Research, Analyst, and Information Technology
Industries: Pharmaceutical Manufacturing

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