Real World Evidence Manager, ROPU ASKAN

BOEHRINGER INGELHEIM SINGAPORE PTE. LTD.; Singapore; On-site; SGD 150,000 - 190,000; Full time

Job summary

Boehringer Ingelheim Singapore Pte. Ltd. seeks an experienced Real World Evidence Manager to drive evidence generation across ASEAN, South Korea, and New Zealand. The role bridges science, business, and patient priorities to inform decision-making.

You will oversee RWE projects (NIS, NTA, IIS, ECR), coordinate timelines and budgets, and engage with HCPs, CROs, and partners while ensuring compliance with regulations. Strong cross-functional collaboration and data storytelling are essential.

Qualifications

• At least 3 years of Real World Evidence work experience, preferably in pharma.
• Knowledge of Real World Evidence design, execution, and reporting.
• Understanding of drug development and commercialization.
• Excellent English communication and stakeholder management.

Responsibilities

• Lead RWE projects including NIS, IIS, ECR across ASEAN, SK, NZ.
• Coordinate planning, approval, execution, reporting, and disclosure.
• Maintain data integrity in CTMS and related platforms.
• Ensure compliance with local and global regulations and SOPs.
• Manage timelines, budgets, risks, and stakeholder alignment.
• Collaborate with Medical Affairs, Market Access, Legal, Procurement, Compliance.

Skills

Project management

Presentation skills

Communication skills

Problem solving

Negotiation skills

Data literacy

Storytelling

Cross-functional collaboration

Prioritization

Education

MPH

MSc in Epidemiology/Health economics/outcomes research

BSc in life sciences

PhD in epidemiology or related

Tools

CTMS

eCTMF

ENCEPP

ClinicalTrials.gov

Job description

THE POSITION

The Real World Evidence (RWE) Manager connect rigorous science, business and patient priorities, generating evidence that changes decisions and improves patient outcomes across diverse markets. It 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). This position 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. It is in charge of leading the gap analysis process regionally and integrated evidence, as well as overseeing all RWE initiatives within ASEAN, South Korea, and New Zealand (ASKAN) region.

Tasks & responsibilities

• Manage Real World Evidence (RWE) projects, including Non-Interventional Studies (NIS), Non-Trial Activities (NTA), Investigator-Initiated Studies (IIS), External Collaborative Research (ECR), digital initiatives, and other evidence-generation activities.
• Provide project, process, and system management support throughout the project lifecycle, from planning and approval through execution, reporting, publication, and disclosure.
• Maintain projects in relevant systems such as CTMS, eCTMF, external funding platforms, and NTA systems, ensuring data accuracy and compliance.
• Ensure all RWE activities comply with local and global regulations, SOPs, business practices, safety reporting, and transparency requirements.
• Oversee project timelines, budgets, risks, and deliverables, ensuring clear stakeholder alignment and communication.
• Support engagements with external experts, healthcare professionals (HCPs), CROs, and research partners, including CRO selection, contracting, and vendor oversight.
• Act as the primary contact for CROs and monitor vendor performance throughout project execution.
• Maintain oversight of the regional RWE portfolio and provide project status updates, reports, and insights to support decision-making.
• Serve as a key user for RWE-related systems and disclosure platforms, including CTMS, eCTMF, ENCEPP, and ClinicalTrials.gov.
• Coordinate cross-functional collaboration among Medical Affairs, Market Access, Legal, Procurement, Compliance, and Corporate stakeholders.
• Drive continuous improvement, best practice sharing, and capability building to strengthen RWE planning, governance, and execution across the ASKAN region.

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.
• At least 3 years of Real World Evidence work experience; ideally in pharmaceutical industry
• Knowledge of Real World Evidence design, execution, and reporting
• Knowledge of the pharmaceutical industry and drug development/commercialization process
• Strategic thinking and ability to translate business and patient needs into evidence-generation plans
• Experience in running clinical studies in the pharmaceutical industry or CRO e.g., database review, registry, is preferred
• Experience working cross-functionally and across countries
• Presentation, project management, communication, problem solving and negotiation skills and gap assessment experience, data literacy and storytelling
• Proven ability to manage priorities, resources, vendors, and external partnerships.
• Excellent organizational, planning, and time management skills.
• Proficiency in written and spoken English.