Graduate - Clinical Operations

MSD in the UK; Greater London; On-site; GBP 26,000 - 34,000; Full time

Job summary

Merck Sharp & Dohme LLC in the UK offers a 24-month Clinical Research Graduate Programme to gain hands-on experience in trial coordination, study management and process improvement.

As a trainee Clinical Trial Co‑ordinator, you will support UK study teams, undertake supervised field visits to trial sites, and receive training on management systems.

Based in Moorgate, London, you will develop practical skills in a global biopharmaceutical environment.

Qualifications

• Completed or expected to complete a BSc degree in Life Sciences, Pharmacy or related discipline.
• Strong planning, analytical and organisational skills.
• Interest in clinical research, healthcare innovation and development of medicines and vaccines.
• Strong attention to detail with documenting and regulatory compliance.

Responsibilities

• Support coordination and delivery of clinical trials, ensuring activities meet study requirements.
• Contribute to clinical research initiatives and continuous improvement activities.
• Maintain essential study documentation and reporting through clinical systems and study management tools.
• Collaborate with study teams and finance partners to support budgeting and forecasting throughout the study lifecycle.

Skills

Adaptability

Budget Development

Clinical IT

Clinical Research

Clinical Trial Management

Data Analysis

Data Management

Drug Development Research

Financial Tracking

Global Clinical Studies

GCDMP

ICH GCP Guidelines

Project Management

Education

BSc in Life Sciences, Pharmacy or related discipline

Job description

Job Description

24-Month Clinical Research Graduate Programme offering hands-on experience in clinical trial coordination, study management, process improvement, and cross-functional collaboration within Clinical Research. As part of the Clinical Research team, you will work as trainee Clinical Trial Co‑ordinator. Providing office-based support to the teams that work on our company clinical programmes in the UK. The opportunity to conduct field visits at trial sites based in the UK under supervision. Throughout your twenty-four months here, you will be given the opportunity to gain a full insight into the principles and practices of a Clinical Research Department within a global company. Working in a professional and friendly environment, you will support the members of our study teams, whilst developing your knowledge and practical skills in setting up and conducting clinical trials. Experiences will include field visits to our trial sites and training on our clinical management systems and processes.

This role will be based in our modern state-of-the-art co-working facilities in Moorgate, London. This site, at the heart of London provides fantastic amenities, support services and collaborative workspaces with convenient transport links.

We are a global biopharmaceutical leader committed to enhancing the lives of individuals through a diverse portfolio of prescription medicines, oncology treatments, life-saving vaccines, and animal health products. Our unwavering dedication to delivering innovative solutions is the driving force behind everything we do.

Responsibilities

• Support the coordination and delivery of clinical trials, ensuring activities are completed accurately, efficiently, and in compliance with study requirements.
• Contribute to key Clinical Research initiatives that support the successful delivery of local studies and continuous improvement activities.
• Manage and maintain essential study documentation and reporting through clinical systems and study management tools.
• Collaborate with study teams and finance partners to support budgeting, forecasting, and financial tracking activities throughout the study lifecycle.
• Build knowledge of clinical research processes, systems, regulations, and best practices through structured training and practical experience.
• Support internal meetings, team events, and cross-functional projects while developing strong stakeholder management and organisational skills.

Requirements

• Completed, or due to complete, a BSc degree (or equivalent qualification) in Life Sciences, Pharmacy, Biomedical Sciences, or a related discipline.
• Demonstrates planning, analytical and organisational skills.
• Interest in clinical research, healthcare innovation, and the development of new medicines and vaccines.
• Strong attention to detail, with the ability to manage documentation, track activities, and maintain accurate records in a highly regulated environment.

Eligibility Criteria for Undergraduates

We are looking for students based in the UK who complete their undergraduate degree between 2025 and 2027.

Important Note

• We do not provide sponsorship for UK work visas during or after the graduate program.
• To be eligible for the 2-year program, you must have the right to work in the UK for its entire duration (Until August 2029).

Start Date

September 2027

Equal Opportunity Employer

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Project Temps (Fixed Term)

Relocation

No relocation

VISA Sponsorship

No

Travel Requirements

No Travel Required

Flexible Work Arrangements

Not Applicable

Shift

Not Indicated

Valid Driving License

No

Hazardous Material(s)

no

Job Posting End Date

10/13/2026

• A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

#UKFT26

Required Skills

Adaptability, Adaptability, Budget Development, Business Process Improvements, Clinical IT, Clinical Research, Clinical Trial Management, Clinical Trials Operations, Clinical Trial Support, Conducting Meetings, Data Analysis, Data Management, Drug Development Research, Financial Tracking, Global Clinical Studies, Good Clinical Data Management Practice (GCDMP), ICH GCP Guidelines, Implement Training Programs, Interpersonal Relationships, Life Science, Meeting Facilitation, Meeting Organization, Prioritization, Process Implementations, Project Management {+ 7 more}