Expire in: 23 days
Our client is a global pharmaceutical organisation conducting novel drug discovery & development projects across a broad range of therapeutic areas including Neuroscience, Inflammation, Immunology and Oncology etc.
In this role you will be supporting the delivery of clinical studies from protocol development through to final reporting and archiving. It’s a great opportunity for someone early in their clinical research career who enjoys organisation, collaboration, and continuous improvement.
Working closely with the Clinical Project Manager, you will help ensure studies run smoothly by coordinating plans, documentation, systems, and partners. You’ll play a central role in keeping teams aligned, maintaining high-quality records, and ensuring timelines and regulatory requirements are met.
Key responsibilities
* Maintain an accurate and audit-ready Trial Master File (TMF) through ongoing review and follow-up
* Support the preparation, review, and finalisation of key study documents (e.g., protocols, amendments, consent forms, plans, submissions, and reports)
* Coordinate meetings, communications, and decision tracking across cross-functional teams and external partners
* Assist with oversight of vendors and investigational sites, including training coordination and issue resolution
* Set up and maintain study data in clinical systems, perform quality checks, and respond to system queries
Key requirements
* Bachelor’s degree (or equivalent) in a relevant scientific, healthcare, or business discipline
* 1–2 years’ experience in clinical research (e.g., trial coordination, monitoring support, or project support)
* Exposure to clinical trials across phases I–IV is advantageous
* Strong attention to detail with the ability to manage multiple priorities
* Confident using office tools and clinical systems, with a focus on data quality
* Clear, professional communication skills and ability to work across global teams
* Proactive, organised, and keen to learn, with a practical approach to problem-solvingAssociate Clinical Project ManagerDo not include the following in your job application, CV, or cover letter:
You should not be asked for payment or irrelevant information. If you have concerns about a job advert or employer, seek guidance on how to proceed.
Looking for your next career move? Join a top company hiring Associate Clinical Project Manager job near me in Slough, Berkshire! This is your chance to work on exciting projects, grow professionally, and enjoy a rewarding career with competitive pay and excellent benefits. Whether you're an experienced professional or looking to take the next step, this role offers the perfect opportunity to enhance your skills and make an impact. Don’t miss out—apply today via Vita CV and take your career to the next level!
© Vita CV: Registered in England and Wales (16187919).
Vita CV uses cookies to enhance your experience, analyze site traffic, and personalize content. By continuing to browse, you agree to our use of cookies.