Senior Director, GMA Study Management

12 - 15 years

25 - 30 Lacs

Posted:14 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

As Senior Director, GMA Study Management, you will drive excellence in study operations, lead a talented team, and collaborate with cross-functional partners worldwide. Your strategic vision and operational expertise will ensure the successful delivery of innovative, high-quality studies that advance patient care and scientific knowledge. Join us to make a meaningful difference on a global scale, while fostering a culture of empowerment, collaboration, and continuous improvement.
 
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, collaborating with Global Clinical Operations (GCO) and Clinical Development (CD) 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.
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

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