Graduate - Clinical Operations

Merck Gruppe - MSD Sharp & Dohme; Greater London; Hybrid; GBP 28,000 - 36,000; Full time

Job summary

Merck Gruppe - MSD Sharp & Dohme in London offers a 24-month Clinical Research Graduate Programme providing hands-on experience in trial coordination, study management, and process improvement within a global biopharmaceutical leader. The role is based at Moorgate, London, with field visits to UK trial sites under supervision.

Training covers clinical management systems, regulatory practices, and cross-functional collaboration.

Qualifications

• BSc degree (or equivalent) in Life Sciences, Pharmacy, Biomedical Sciences, or related discipline.
• Strong planning, analytical and organisational skills.
• Interest in clinical research, healthcare innovation, and development of new medicines and vaccines.
• High attention to detail and ability to manage documentation in a regulated environment.

Responsibilities

• Support coordination and delivery of clinical trials, ensuring activities are accurate and compliant.
• Contribute to Clinical Research initiatives supporting local studies and continuous improvement.
• Manage and maintain essential study documentation and reporting through clinical systems.
• Collaborate with study teams and finance partners for budgeting, forecasting and financial tracking.
• Build knowledge of clinical research processes, systems, regulations, and best practices through training.
• Support internal meetings, team events and cross-functional projects with stakeholder management.

Job description

Location London, London, United Kingdom Job Type Full time

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‑Ordinateur. Providing office‑based support to the teams that work on our company clinical programs 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 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).

Required Skills

• 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

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.

Start Date

September 2027

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

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