Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. 

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. 

Make an Impact as an Associate Clinical Data Manager at Worldwide

Clinical data plays a critical role in advancing research and ensuring high-quality clinical trial outcomes. As an Associate Clinical Data Manager, you will support the delivery of accurate, reliable, and timely clinical data, helping study teams make informed decisions throughout the trial lifecycle.

Working closely with Lead Data Managers and cross-functional teams, you will contribute to study start-up, conduct, and close-out activities while ensuring data quality and compliance with study requirements. Your work will directly support the successful execution of clinical trials and the delivery of results that matter.

This is an excellent opportunity for a clinical data professional looking to build upon their data management experience, expand their technical expertise, and take ownership of key study activities within a collaborative global environment.

Where You'll Work

This is a remote role open to candidates based in United Kingdom. You will collaborate with global teams across multiple time zones.

What You'll Do

• Support Lead Data Managers with study start-up, conduct, and close-out activities across assigned clinical trials.
• Prepare and maintain key data management documentation, including Data Management Plans (DMPs), CRF Completion Guidelines (CCGs), and Data Transfer Agreements (DTAs).
• Perform and support user acceptance testing (UAT) for new study database builds and mid-study updates.
• Review, clean, and validate clinical trial data to ensure accuracy, completeness, and quality.
• Reconcile data from external sources such as Serious Adverse Events, IRT systems, and central laboratories.
• Generate and maintain study reports in accordance with study documentation and reporting requirements.
• Support database lock activities to help ensure timely study milestones and deliverables.
• Contribute to process improvement initiatives by providing feedback and recommendations to data management leadership and subject matter experts.
• Act as Lead Data Manager for one or more studies when required.

What You'll Bring

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience.
• 1–3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
• Proficiency in English.
• Strong attention to detail with a commitment to data accuracy and quality.
• Good written and verbal communication skills and the ability to collaborate effectively with study teams.
• Basic knowledge of clinical data management methodologies, best practices, and technologies.
• Basic understanding of clinical trial processes and key study documents, including protocols, statistical analysis plans, CRFs, and study reports.
• Ability to manage assigned responsibilities effectively while contributing to the successful delivery of clinical trial data.

Discover the Difference

We love knowing that someone is going to have a better life because of the work we do.  Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.