Associate Director / Medical Writer - Real-World Evidence

1w1 week ago

Ipsos

Singapore, SG · Full-time · S$180,000 – S$280,000

About this role

As Associate Director / Medical Writer – Real-World Evidence, draft, edit, and finalise scientific documents including study protocols, statistical analysis plans, study reports, manuscripts, abstracts, and conference posters. Translate complex data from real-world studies like retrospective analyses, registries, and chart reviews into clear, compelling narratives for different audiences. Support development of evidence summaries, value dossiers, slide decks, and client-facing materials.

Ensure all written materials are scientifically accurate, clearly presented, and aligned with project objectives and client requirements. Adhere to relevant publication standards, data privacy requirements, and ethical guidelines. Participate in internal quality review processes and incorporate feedback to deliver high-standard outputs.

Work closely with project managers, epidemiologists, and data analysts to ensure scientific accuracy and consistency across deliverables. Contribute to project planning discussions, helping shape communication strategies and timelines. Support literature reviews and background research to inform study design and contextualise findings.

Join Ipsos, one of the world’s largest research companies managed by researchers and ranked #1 full-service research organization for four years. With presence in 90 markets and over 75 data-driven solutions, collaborate with global experts to deliver top-quality research for 5000+ clients. Proudly Great Place to Work Certified in 2022 & 2023.

Requirements

2–5 years of experience in medical writing, scientific communication, or related roles in the life sciences sector (consultancy, CRO, pharma, or academia)
Proven ability to write clear, accurate, and engaging scientific content for a variety of audiences
Strong understanding of clinical research, epidemiology, or real-world evidence generation
Excellent attention to detail, with strong editing and quality-control skills
Ability to manage multiple projects simultaneously and deliver high-quality work under deadlines
Advanced degree (MSc, MPH, PhD, PharmD, or similar) in life sciences, public health, epidemiology, or a related field preferred
Strong command of written English; additional Asian languages are a plus

Responsibilities

Draft, edit, and finalise scientific documents including study protocols, statistical analysis plans, study reports, manuscripts, abstracts, and conference posters
Translate complex data from real-world studies (e.g., retrospective analyses, registries, chart reviews) into clear, compelling narratives tailored to different audiences
Support the development of evidence summaries, value dossiers, slide decks, and other client-facing materials
Ensure all written materials are scientifically accurate, clearly presented, and aligned with project objectives and client requirements
Adhere to relevant publication standards, data privacy requirements, and ethical guidelines
Participate in internal quality review processes and incorporate feedback to deliver high-standard outputs
Work closely with project managers, epidemiologists, and data analysts to ensure scientific accuracy and consistency
Contribute to project planning discussions and support literature reviews