Real World Evidence (RWE) Manager

We are IMETA

ROPU IMETA is a Regional Operating Unit consisting of 6 mid-sized Operating Units: India, Turkey, Southern Africa (South Africa & Sub Sahara Africa) Northeast & West Africa, Near East & UAE, Saudi Arabia, Gulf & East Africa (SAGEA).

IMETA is home to more than 47 nationalities. We are a myriad of color and culture and embracing this diversity is one of our greatest opportunities.
We are a powerhouse of talent, and we work together to ensure that we grow, nurture, and retain our talent. Uniting and working together is the key to our success.

The Position:

The Real-World Evidence (RWE) Manager supports the Medical Affairs and Market Access teams by coordinating the operational aspects of RWE projects and processes, including the development, conduct, reporting and disclosure of these activities (e.g. NIS, NTA, ECR) . RWE manager will contribute to improved oversight and process adherence for RWE activities, enhanced collaboration both cross-functionally/cross-regionally and between the company and external collaborators, and the generation of high-quality RWE to inform internal and external decision making.

This role will report to the Regional Head of Quality Medicine, Real World Evidence & Medical Excellence Human Pharma.

Responsibilities:

• Oversee and manage RWE projects, including Non-Interventional Studies (NIS), Non-Trial Activities (NTA), Investigator-Initiated Studies (IIS), External Collaborative Research (ECR), and digital initiatives.
• Collaborate with Project Owners in Medical Affairs or Market Access teams and country organizations to ensure successful project execution across all phases (development, approval, conduct, reporting, and transparency).
• Set up and manage projects in relevant systems (e.g., CTMS, eCTMF, external funding platforms) while ensuring compliance with local/global regulations, SOPs, and safety/disclosure requirements.
• Facilitate communication and alignment between internal teams and external stakeholders (e.g., HCPs, CROs). Provide support to external collaborators for funding applications and activity management.
• Conduct gap analyses, develop local RWE plans, and integrate cross-functional perspectives to generate relevant data and evidence. Provide strategic input on RWE activities and ensure accurate oversight of project status and budgets.
• Lead CRO selection, contracting, and monitoring in collaboration with Medical Advisors, purchasing, and legal teams. Act as the primary contact for CROs.
Serve as a key user for RWE systems (e.g., CTMS, eCTMF, disclosure platforms) and support cross-functional teams in process coordination, best practice sharing, and continuous improvement initiatives.

Requirements:

• Relevant degree (e.g. MPH, MSc, BSc, or Ph.D. in epidemiology, health economics/ outcomes research, medicine, pharmacy/pharmacology, life sciences or similar) or other professional training combined with training and experience working with real-world data.
• Minimum 5 years of pharmaceutical industry experience with minimum 2 years of Real-World Evidence work experience.
• Experience in running clinical studies in the pharmaceutical industry or CRO e.g., database review, registry, is preferred.
• Excellent Knowledge of the pharmaceutical industry and drug development/commercialization process.
• Expertise in Real World Evidence design, execution, governance and reporting.
• Protocol writing, understanding of different types of data sources, methodologies, and relevant software
• Effective planning and analytical skills
Collaborative and efficient project management.

What’s Next?

We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.

Screening:

In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.