About Parexel

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®.

About the Role

We are seeking experienced Global Study Managers (GSM) with strong oncology trials experience to join our team in a remote capacity in the UK. As a GSM you will be responsible for global study activities from start up through conduct and study close.

The Global Study Operations Manager has responsibility for study management aspects of assigned studies, including vendor and budget management.

You will support clinical research activities that advance new treatments for patients and collaborate with global cross‑functional teams.

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 Global Study Manager can explore career paths and expand skills across clinical research.

These will be fully remote home-based positions.

Key Responsibilities

• Global Study level implementation of Start-up and Site Activation Plans

• Responsible for global/regional study level Recruitment Strategy

• Responsible to support the development of global study level plans

• Communication with both global and local teams, internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans

• Responsible for study vendor management and oversight including follow up and coordination of vendor deliverables

Candidate Profile

You’ll thrive in this role if you bring:

• Extensive experience in clinical trial project management across international trials

• Global experience working in clinical research, healthcare, or a regulated environment

• The ability to collaborate across teams and communicate clearly

• A patient‑focused mindset and strong attention to detail

• The ability to work independently and exercise your own judgement

Required Qualifications

• M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential. (Master’s is preferred)

• Minimum of 5 years’ relevant experience in clinical trial management

• Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.

• Strong communication, organization, and problem‑solving skills

• Fluency in English, both written and spoken

• Prior and demonstrable experience working at a senior level within Study start up is preferred.

If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.