Real World Evidence Manager, ROPU ASKAN (Singapore, Singapore, Central Singapore)

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.

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