Clinical Trial Manager; Oncology; UK; Home-based; FSP

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is a leading global clinical development partner delivering insights‑driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient‑focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry‑leading innovation, With Heart®.

We are seeking a Clinical Trial Manager (CTM) to join our team in a remote capacity in the UK. As a CTM, you will act as a member of the sponsor’s Development Operations team and will manage individual clinical trials and/or programs as part of their Clinical Trial Working Group.

You’ll join a fast‑paced, growth‑oriented environment focused on making a meaningful impact through the set‑up, execution and delivery of assigned trials and contribute to delivery of the sponsors pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.

With diverse teams and continuous learning opportunities, the Clinical Trial Manager can explore career paths and expand skills across clinical research.

• Manage external vendors and contract research organisations.
• Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual.
• Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents.
• Assist with protocol development and study report completion.
• Manage monitoring activities (may include routine on‑site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols.
• Provide guidance, direction, and management to CRAs.
• Track patient enrollment; qualify, initiate, monitor, perform closeout activities, and review site reports; and assist in coordination of data management activities.
• Coordinate study supplies.
• Negotiate contracts with vendors of clinical trial services.
• Review Informed Consent Forms, CRFs, and study related materials.
• Plan and participate in investigator meetings.
• Assist and support data query process.
• Assure regulatory compliance of investigational sites with sponsor’s SOPs and FDA and ICH guidelines.
• Ensures trial master file is current and maintained.

Please note that responsibilities may require a work schedule that may include working outside of “normal” work hours, to meet business demands.

You’ll thrive in this role if you bring:

• Experience in clinical trial project management, preferably across international trials.
• The ability to collaborate across teams and communicate clearly.
• A patient‑focused mindset and strong attention to detail.

• Bachelor’s, nursing…