Clinical Database Programmer

Medpace

Greater London

On-site

GBP 45,000 - 60,000

Full time

29 hours ago
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Benefits offered by this job

Competitive compensation
Health benefits
WFH flexibility
Social events

Job summary

Medpace is seeking a full-time, office-based Clinical Database Programmer to join our Data Management team in London. You will help develop databases for clinical data capture and processing for analysis and reporting, collaborating with study teams to ensure timely, high-quality database delivery.

You will coordinate with Data Managers, perform validation, and gain knowledge across multiple EDC systems while contributing to global project teams in a fast-paced CRO environment.

Qualifications

  • Bachelor’s degree in computer science, mathematical science, life science or related field.
  • Basic level experience in at least one programming language.
  • Rave and/or C# or similar programming experience preferred.
  • Flexible and able to support a variety of studies.
  • Meticulous attention to detail.

Responsibilities

  • Coordinate with Data Managers to develop and maintain clinical study electronic data capture (EDC) databases according to company and/or sponsor standards;
  • Perform quality checks and validation testing in collaboration with colleagues in order to deliver a quality product to our Sponsors;
  • Gain and strengthen knowledge in the industry and in multiple electronic data capture systems;
  • Be an active member of multiple global project teams, and collaborate across several different functional areas.

Skills

Basic programming experience
RAVE
C#

Education

Bachelor’s degree in computer science, mathematical science, life science or related field

Tools

Rave
C#

Job description

Our global business is growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Data Management team in our London office. The position will work in a team to develop databases in which clinical data is captured and processed for analysis and reporting. This position plays a critical role on our study teams and quality, timely database development is instrumental to the company’s success. If you are interested in an exciting career where you have the opportunity to use your knowledge and expertise and can develop and grow your career even further, then this is the position for you!

Responsibilities
  • Coordinate with Data Managers to develop and maintain clinical study electronic data capture (EDC) databases according to company and/or sponsor standards;
  • Perform quality checks and validation testing in collaboration with colleagues in order to deliver a quality product to our Sponsors;
  • Gain and strengthen knowledge in the industry and in multiple electronic data capture systems;
  • Be an active member of multiple global project teams, and collaborate across several different functional areas.
Qualifications
  • Bachelor’s degree in computer science, mathematical science, life science or related field;
  • Basic level experience in at least one programming language;
  • Rave and/or C# or similar programming experience preferred, but not required;
  • Flexible and able to support a variety of studies;
  • Meticulous attention to detail
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.

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