NHS Professionals - Career Event: Clinical Trial Management – Medpace, London

Medpace; Greater London; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is inviting NHS and University professionals to transition into the clinical trials sector. This unique recruitment event in Central London offers a chance to learn from experienced industry insiders and explore opportunities within a global CRO. Attendees will gain insights into the clinical trial manager role while receiving foundational training to enhance their careers in drug development. Join a passionate team dedicated to improving patient outcomes and making a significant impact in the healthcare landscape.

Benefits

Flexible work environment

Competitive compensation and benefits package

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifications

• Experience in clinical trials from NHS or University settings.
• Fluency in English with strong presentation skills.

Responsibilities

• Manage day-to-day operations of clinical studies.
• Serve as primary contact for operational project-specific issues.
• Develop operational project plans and manage study vendors.

Skills

Clinical Trials Management

Presentation Skills

Team Collaboration

Risk Management

Education

Degree in Medicine or Life Sciences

Clinical Research Certification

Job description

Job Summary

NHS or University clinical research professional, considering a change to the Industry?

Medpace is delighted to host a recruitment event tailored to professionals working in the NHS or Academic setting (Clinical Trial Managers, Junior Doctors, Clinical Research Coordinators, Clinical Research Nurses, Clinical Practitioners etc) to be considered for the Clinical Trial Manager position at Medpace.

This is a rare and exciting opportunity for individuals seeking to make a switch to the clinical trials industry!

Join the Medpace hiring team for an exclusive onsite event at our London Office to hear from former NHS and University-lead clinical research professionals who made the switch into the private industry and discover how to transform your career at a global CRO.

LOCATION: Central London

DATE: Thursday 10th July 2025

APPLICATION CLOSE DATE: Monday 7th July 2025

This is an opportunity for public sector professionals to enter the industry, to receive solid foundational training, work in an international environment, and accelerate their career in the research and development of cutting-edge therapeutics. Attendance at this event will act as a first step in eventually obtaining a position with us.

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.

Responsibilities

Clinical Trial Manager:

• Manage and provide accountability for day-to-day operations of the studies conducted by Medpace on behalf of Biotech sponsors, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, SOPs and regulations
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables
• Maintain in depth knowledge of protocol, therapeutic area, and indication
• Lead internal project team and Provide cross-functional oversight of study team deliverables.
• Review and provide input for study protocol, database edit check specifications and final study report, when applicable
• Develop study-specific operational project plans
• Implement and manage a risk-based approach to project execution
• Responsible for management of study vendors
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables, including CRA trip report review

Qualifications

• Experience in clinical trials from an NHS and / or University setting (Clinical Trial Managers, Junior Doctors, Clinical Research Coordinators, Clinical Research Nurses, Clinical Practitioners etc).
• A background in one of our key therapeutic focus areas is of advantage, but not a must: Oncology, Cardiovascular, Renal / Gastrointestinal, Nuclear Medicine, Haematology or Radiopharmaceuticals
• Fluency in English with solid presentation skills
• Ability to work in a fast-paced dynamic industry within an international team
• Please include your cover letter in your application submission

Medpace Overview

Medpace 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

• Flexible work environment
• Competitive compensation and benefits package
• Competitive annual leave packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

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.

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