Senior Medical Data Reviewer

Senior Medical Data Reviewer

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Senior Medical Data Reviewer at ICON, you will provide expert medical oversight of clinical trial data, ensuring accuracy, consistency, and patient safety. You will support complex programmes, mentor colleagues, and contribute to the development of robust medical review practices.

What You Will Do:

You will take ownership of clinical research deliverables, applying your expertise to complex challenges.

Key responsibilities include:

• Performing advanced medical review of clinical data listings, patient profiles, and safety datasets to assess plausibility, consistency, and protocol adherence.
• Identifying trends, potential safety signals, or data quality issues and collaborating with study teams to drive resolution.
• Contributing to or leading the development of medical review plans, guidelines, and tools for complex studies or programmes.
• Providing medical input into database lock readiness, interim analyses, and regulatory submission preparation.
• Collaborating with pharmacovigilance, biostatistics, and data management to support integrated safety and efficacy evaluations.
• Mentoring junior medical data reviewers and supporting continuous improvement of review methodologies.

Your Profile:

You will have a strong foundation in clinical research, with the experience to work independently and guide others.

Required qualifications and experience:

• Medical degree or advanced clinical qualification (e.g., MD, MBBS, PharmD) with relevant clinical experience.
• Extensive experience in clinical research, medical monitoring, pharmacovigilance, or related roles within CRO, pharma, or biotech.
• Deep understanding of clinical trial design, GCP, safety reporting, and medical terminology.
• Excellent analytical and critical-thinking skills, with a high level of attention to detail in data review.
• Strong communication and collaboration skills, with experience working in cross-functional, global teams.
• Ability to manage multiple studies and priorities while maintaining high quality and timelines.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply