Medpace
Clinical Data Reviewer - Oncology
Bio and life sciences
This role has closed. It is kept here for your records.
- Location
- London
- Opened
- 3 Aug 26
- Closes
- No date listed
UK visa sponsorship
Medpace UK Limited is on the gov.uk register of licensed sponsors.
Rating: A rating
Routes: Skilled Worker, Global Business Mobility: Senior or Specialist Worker
A licence means the employer can sponsor; it does not promise this role is sponsored. Check the posting.
Does Medpace sponsor UK visas? Licence and open rolesAbout the role
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Reviewer to join our Global Clinical Coding & Support team.
This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous nursing expertise and can develop and grow your career even further, then this is the opportunity for you!
*Stable schedule with no weekends, no work on Medpace holidays, and flexible work schedule*
Responsibilities
Comprehensive manual review of clinical data collected in trials
Development of clinical review guidelines for specific therapeutic areas
Interface with Data Management team to assure query resolution
Seeking specialisation in Oncology
Qualifications
Bachelor’s Degree in Nursing, or more advanced clinical degree
Professional / or Post-Qualification Nursing experience, preferably in Oncology
General knowledge of clinical trial processes and/or experience working with clinical data
TRAVEL: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.