RWE Program Lead, ASKAN Region

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

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.