Job Description

12-Month Clinical Research Student Placement offering hands-on experience in clinical trial coordination, study management, regulatory processes, and site-facing clinical research activities.

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 programs in the UK. The opportunity to conduct field visits at trial sites based in the UK under supervision Throughout your twelve 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 study teams in the day-to-day coordination and delivery of clinical trials across a range of activities.
• Assist with the preparation, maintenance, and management of study documentation to support regulatory and ethics submissions.
• Support budgeting and financial tracking activities throughout the clinical trial lifecycle.
• Gain exposure to clinical trial sites by participating in on-site monitoring activities alongside experienced clinical research professionals.
• Contribute to departmental initiatives, meetings, and events while building knowledge of clinical research processes and best practices.
• Develop an understanding of clinical trial systems, regulations, and operational activities through structured training and practical experience.
  

Requirements:

• You must be currently studying at a UK university and will be looking to complete a 12-month student internship as part of your undergraduate degree.
• Studying towards a degree in Biomedical Sciences, Pharmaceutical Sciences or a related life sciences discipline.
• Working knowledge of Microsoft Office packages (e.g. Word, Excel, PowerPoint)
• Demonstrates an appreciation of current topics in clinical research and clinical trial conduct

 

How to Apply (Please Read):

Please complete the online application form by answering questions within the application and upload your CV and Cover Letter in a combined document in the ‘resume/CV’ section.

 

Our standard Future Talent recruitment process is: An online application, a virtual conversation and then a final assessment.

 

Next Steps:

In the event of your successful progression to the next stage, one of our future talent team will contact you within two - three weeks of the application closing date. 

 

Start Date:

June 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.

 

For more Information visit our Future Talent page!

 

#UKFT26

 

 

Required Skills:

Analytical Problem Solving, Analytical Problem Solving, Biomedical Research, Clinical Data Interpretation, Clinical Reporting, Clinical Research, Clinical Research Operations, Clinical Trial Development, Clinical Trial Management, Clinical Trial Management Systems (CTMS), Clinical Trials Monitoring, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, Health Economics, Life Science, Observational Studies, Office Applications, Patient Support, Patient Support Programs, Process Improvements, Project Management, Regulatory Documents {+ 7 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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:

Intern/Co-op (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.