Clinical Study Project Manager

Join PHARMExcel, an award-winning CRO where collaboration, expertise and a shared passion for improving patient outcomes drive everything we do.

As a growing organisation, we combine the flexibility of a remote-first culture with the support of a close-knit team, giving you the opportunity to work on exciting projects alongside industry-leading experts. You will collaborate with Key Opinion Leaders, world-class academics and innovative entrepreneurs across the Biotech and MedTech sectors, building your experience through diverse and meaningful clinical research programmes.

At PHARMExcel, you'll be supported to learn, develop and grow your career while making a genuine impact within a collaborative and people-focused environment.

About the role:

As a Clinical Study-Project Manager (CSPM) at PHARMExcel, you will lead the delivery of clinical studies with precision, expertise and a strong focus on quality. Whether it is an advanced therapy trial, drug trial, non-interventional study or medical device clinical investigation, you will be the driving force behind your studies, ensuring successful delivery from start-up through to close-out.

As the primary point of contact for clients and the clinical operations team, you will build strong relationships and ensure integrity, compliance and excellence throughout every phase of study delivery.

You will be part of a supportive and welcoming team that is passionate about helping each other grow and succeed. We are looking for someone who will bring the same positive, collaborative and solutions-focused approach to the role.

You will:

• Oversee the full lifecycle of clinical studies, ensuring delivery to agreed timelines, budgets and regulatory requirements.
• Act as a role model and mentor, supporting and developing junior team members through the sharing of knowledge, expertise and best practice.
• Collaborate with fellow CSPMs and senior operational leaders to drive continuous improvement, innovation and operational excellence.
• Take ownership of study delivery, ensuring projects remain on track, within budget and consistently exceed client expectations.
• Build effective relationships and work collaboratively across internal teams, sponsors, sites and external stakeholders.
• Champion quality, compliance and continuous improvement across all aspects of study delivery.
• Contribute to departmental objectives and support senior management in achieving strategic and operational goals.

You will bring:

• 5+ years' experience in clinical operations, study management or project management within a CRO, biotech or pharmaceutical environment
• Experience leading complex clinical studies from start-up through to close-out
• Strong knowledge of ICH-GCP and clinical research regulations
• Excellent stakeholder management and client relationship skills
• A proactive, solutions-focused approach with strong organisational skills
• The ability to balance quality, timelines and budgets while delivering exceptional client outcomes

We offer:

• Competitive pay + company bonus (performance based)
• Generous annual leave + your birthday off
• Private medical insurance
• Remote-first culture with flexible working
• Learning & development opportunities
• Family-friendly policies
• Professional memberships paid for
• 24/7 confidential Employee Assistance Programme (EAP)
• Wellbeing, ESG, and charity initiatives
• Supportive and collaborative work culture

Ready to Make a Difference?

If you are interested in joining our team, please send your CV and a covering letter, including your salary expectations, to careers@pharmexcel-cro.com. We look forward to hearing from you.