Intern Clinical Trial Coordinator

Job Description

As part of the Clinical Research team, you will work as trainee Clinical Trial Co-Ordinator: a. Providing office-based support to the teams that work on our company clinical programs in the UK & ROI b. 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.

Duties Proprietary

• Work on assigned project(s) under supervision

• Assist the study team in their daily activities

• Understand, develop and manage study documents relating to regulatory and ethics submissions

• Generate study budgets and review payments

• Field visits to trial Sites under supervision

• Participate in department level events such as Department and Townhall meetings and visits by internal or external guests.

Technical Specifications

• You will be looking to complete a 12-month placement in your third or penultimate year of study, returning to your course at the end of the placement

• Studying 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 Qualities we look for

• Demonstrates strong organisational skills

• Demonstrate strong analytical skills

• Operates with a high level of integrity, transparency and accountability

• Comprehends and aligns with our organisation’s core values

• Aligns and fosters a culture of diversity and inclusivity

• Demonstrates initiative, proactivity and academic curiosity

• Encourages and boosts their colleagues through teamwork

• Demonstrates clear and effective communication and demonstrates a desire to learn and improve their performance through feedback

Next Steps:

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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Analytical Problem Solving, Biological Sciences, Biomedical Sciences, Biopharmaceuticals, Biopharmaceutics, Business Integrity, Clinical Research, Clinical Testing, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, Life Science, Office Applications, Pharmacology, Process Improvements, Project Management, Reporting and Analysis, Site Initiation

 Preferred Skills:

Job Posting End Date:

10/7/2025

*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.