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.

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Share:

Location

Dublin, Warsaw, Johannesburg, Bratislava, Reading

Reference: JR162407

Benefits & Rewards

Inclusion & Belonging

Career Pathways

Environmental, Social & Governance

Inside ICON

Content type

Blogs

Publish date

01/17/2025

Summary

Five Reasons Why You Should Work at a Contract Research Organization

Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities tha

If you’re seeking a rewarding and fulfilling work environment, a career at a CRO might be the perfect fit.

Read more

Tips to make a lasting impression in a video interview

Career Progression

Publish date

05/10/2024

Summary

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video

Ace your virtual job interview with these proven video interview tips.

Read more

4 life sciences jobs that are taking off

Publish date

11/24/2022

Summary

Life sciences are undeniably an exciting area to start and pursue a career in.

In fact, the global life sciences space is predicted to be worth a massive $2 trillion in gross value by 2023. Co

Life sciences are undeniably an exciting area to start and pursue a career in.

Read more

View all

Similar jobs at ICON

Clinical Trial Liaison

Salary

Location

US, Blue Bell (ICON)

Location

Texas

North Carolina

Ohio

Rhode Island

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Liaison

Job Type

Permanent

Description

• As a Clinical Trial Liaison at ICON, CTLs combine deep therapeutic and scientific knowledge with strategic agility to influence investigators, elevate protocol understanding, and co-develop tailored e

• Reference

• JR162159

• Expiry date

• 01/01/0001

• Author

• Jamie Pruitt

• Read more

• Shortlist Save this role

• Read more

• Shortlist Save this role

• Medical Director

Salary

Location

UK, Reading

Location

Sofia

Copenhagen

Warsaw

Lisbon

Bucharest

Barcelona

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Medical Director

Job Type

Permanent

Description

• As a Medical Director at ICON, you will drive medical initiatives within project teams, guiding strategic direction and decision-making processes, and offer expert medical and scientific guidance, le