Entry Level - Clinical Research Associate

Role overview

Medpace is hiring an entry-level Clinical Research Associate for a full-time role based in London. This position is suited to people with a background or strong interest in medicine, health, or life sciences who want to build a career in clinical research, support the development of drugs and medical devices, and contribute to bringing new therapies to patients. The role involves travel across the UK and is initially fully office-based, so candidates must live within commuting distance of the central London office to make the most of the training provided.

Who tends to succeed in this role

Medpace notes that successful CRAs often come from a variety of healthcare and science-related backgrounds, including nursing, dietetics, pharmacy support, pharmaceutical or device sales, biotechnology engineering, PhD or Pharm.D studies, health and wellness coordination, site coordination, clinical research coordination, and research assistance.

PACE training program

Selected candidates join the PACE® Training Program, designed to help them develop the confidence and practical knowledge needed to perform CRA duties effectively. The program uses interactive learning, guided discussion, and hands-on exercises to strengthen core CRA capabilities and support the transition toward working independently.

Key advantages of the role

This position offers a dynamic work environment with changing day-to-day responsibilities, exposure to multiple therapeutic areas, close collaboration with regulatory and therapeutic experts, a defined path for promotion and career growth, and the possibility of mentoring and management opportunities. Compensation is described as competitive and includes a bonus program.

Responsibilities

• Carry out site qualification, initiation, monitoring, and closeout visits in line with the approved protocol.
• Maintain regular communication with site staff, including coordinators, physicians, and other team members.
• Check that investigators have the appropriate qualifications, training, staffing, tools, facilities, and laboratory support needed for the study.
• Compare medical records and source documents with case report form entries, flag errors to site teams, support good documentation practices, and report protocol deviations according to SOPs, GCP, and regulatory standards.
• Confirm that only eligible participants are being enrolled by the investigator.
• Review regulatory documents.
• Track accountability and inventory for investigational products and/or medical devices.
• Review adverse events, serious adverse events, concomitant medications, and related illnesses to ensure data is reported accurately and in line with the protocol.
• Evaluate site performance in patient recruitment and retention and suggest improvements where needed.
• Prepare monitoring reports and follow-up letters summarizing findings, deviations, deficiencies, and recommended corrective actions to help ensure compliance.

Qualifications

• A bachelor’s degree is required; a background in health or life sciences is preferred.
• Candidates should be prepared to travel nationally about 60% to 80% of the time.
• Working knowledge of Microsoft Office is needed.
• Strong communication and presentation abilities are an advantage.
• A valid driver’s licence is mandatory.
• Applicants must be willing to work fully from the office during the main training period.

About Medpace

Medpace is a full-service clinical contract research organization supporting Phase I to Phase IV development for biotechnology, pharmaceutical, and medical device companies. The company focuses on accelerating the development of safe and effective treatments through a scientific, disciplined approach and combines local regulatory and therapeutic expertise across major disease areas. It is headquartered in Cincinnati, Ohio, and employs more than 6,000 people across over 40 countries.

Why join Medpace

Medpace emphasizes people, purpose, and passion, with a mission to make a meaningful difference now and in the future. The organization says its work over more than 30 years has benefited patients and families across many disease areas.

Perks and benefits

• Flexible working environment
• Competitive compensation and benefits
• Competitive paid time off packages
• Structured career progression with professional growth opportunities
• Company-sponsored employee appreciation events
• Health and wellness initiatives for employees

Awards

• Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
• Has repeatedly received CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility.

Next steps

A member of the Medpace team will review applications and contact shortlisted candidates with the next steps.