Job Description

Job Description: As a Global Project Manager, Real-World Evidence , you will lead complex, global real-world evidence studies and non-interventional studies. You will be responsible for strategic planning, execution, and oversight of these projects, ensuring timely delivery, high-quality outcomes, and compliance with regulatory requirements. Key Responsibilities: Strategic Leadership: Develop and implement strategic frameworks for real-world evidence studies, aligning with global business objectives. Identify and prioritize key research questions and study designs. Collaborate with cross-functional teams to develop innovative and impactful real-world evidence strategies. Project Management Excellence: Lead and manage complex, global real-world evidence studies from initiation to closure. Develop and implement robust project plans, timelines, and budgets. Oversee vendor selection, contract negotiation, and performance management. Proactively identify and mitigate risks, develop contingency plans, and ensure project deliverables meet quality standards. Regulatory and Compliance: Ensure adherence to regulatory requirements (e.g., GCP, ICH-GCP, GDPR) and ethical guidelines for real-world studies. Collaborate with regulatory affairs to obtain necessary approvals and ensure compliance throughout the project lifecycle. Stakeholder Management: Build strong relationships with key stakeholders, including clinical operations, medical affairs, regulatory affairs, and external partners. Effectively communicate project status, risks, and opportunities to stakeholders at all levels. Proactively address challenges and resolve conflicts to ensure project success. Requirements: Education: Advanced degree (Masters or PhD) in a relevant field (e.g., life sciences, health economics, epidemiology, statistics). Experience: 5-7 years of relevant experience in project management, clinical research, or real-world evidence. Language Skills: Fluency in written and spoken English. Competency Profile: Strong leadership skills and the ability to motivate and inspire teams. Proven track record of successfully leading complex, global projects. Deep understanding of real-world evidence methodologies and technologies. Excellent communication and interpersonal skills. Strong analytical and problem-solving skills. Ability to work independently and collaboratively 1 in a cross-functional team. Knowledge of regulatory requirements and ethical guidelines for clinical research and real-world evidence. About Novo Nordisk: Novo Nordisk, a global healthcare leader, is seeking a Senior Global Project Manager to join our Real-World Evidence Operations team in the Regions Operations Department of Global Medical Affairs, Global Business Services (GBS), based in Bangalore. Why Join Novo Nordisk: Impactful Work: Contribute to groundbreaking real-world evidence studies that shape healthcare decisions. Collaborative Culture: Work with a talented and diverse team of experts. Career Development: Benefit from ongoing professional development opportunities and a supportive work environment. Global Impact: Be part of a global healthcare leader making a difference in peoples lives. To apply, please email your resume and a cover letter highlighting your relevant experience and qualifications to [email protected] with the subject line "Senior Global Project Manager, Real-World Evidence Application - Bangalore." Novo Nordisk is an equal opportunity employer. We value diversity and encourage individuals from all backgrounds to apply. Disclaimer Related jobs