Data Manager (Clinical Trials)

Our corporate activities are growing rapidly, and we are currently seeking a Clinical Data Manager to join our UK Data Management team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. This role takes on the responsibility as a leader in data management tasks which take place for the entire duration of a clinical trial. The Data Management team works in conjunction with other departments within Medpace to ensure high data quality. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
Develop and review Data Management procedures for clinical trials with sponsor companies and other departments;
Lead the design and validation of the CRF specifications and edit checks for the electronic data capture system used for each study;
Coordinate overall Data Management by serving as primary contact for the sponsor, external data providers, and all project team members;
Interact with external data providers, and all project team members in the cross functional team; and
Attend bid defence meetings, teleconferences and face to face sponsor meetings as the lead representative from Data Management.
Qualifications Bachelor’s Degree in a Science or Mathematics related field with strong Data Management experience in Clinical Trials; OR
Master’s Degree in a Science or Mathematics related field with good Data Management experience in Clinical Trials;
Experience operating as primary contact for Data Management activities, including project oversight and direct vendor or client interaction;
Computer experience with database, spreadsheet, and EDC software (i.e. SAS, Oracle Clinical, and/or Rave preferred);
Possess an understanding of database structure and processes in data management; and
A basic knowledge of medical terminology is needed, as well as knowledge of clinical research methodologies.
Medpace OverviewMedpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
Hybrid work-from-home options (dependent upon position and level)
Competitive PTO packages
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Flexible work schedule
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
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