As an ISO 9001 certified, organisation PHARMExcel prides itself in delivering high quality and results driven clinical services. Our broad portfolio ranges from non -interventional, CTIMP, ATMP, rare disease and medical devices investigations. You will be working with the best of the best including key opinion leaders, world class academics and entrepreneurs across the biotech and medtech sectors.
About the role
As a Senior CS-PM at PHARMExcel, you will take key responsibility for the execution and delivery of your client’s programme of work. Whether it is an advanced therapy trial, drug trial, non-interventional or medical device clinical investigation, you will be the driving force behind your studies.
As the main point of contact for our clients and clinical operations team, you will ensure integrity, compliance, and excellence in every phase of trial delivery.
We’re looking for a leader and a driver-someone who is not afraid to challenge the status quo. You will be confident and knowledgeable, building trust with your clients by guiding and supporting them.
At PHARMExcel you’ll be part of our supportive and welcoming team that is all about helping each other grow. We are looking for someone who will bring that same positive, collaborative spirit to the role of Senior Clinical Study-Project Manager.
You will:
- Be responsible and accountable for your allocated clinical studies and investigations
- Be a role model and mentor, guiding junior team members with clinical expertise and confidence.
- Work alongside your fellow CSPMs and the Senior operational leaders to help shape and drive progress and change.
- Work autonomously, ensuring studies are on time, on budget, and exceed client expectations.
- Work flexibly and collaboratively across internal functions and external stakeholders.
- Champion quality, innovation, and continuous improvement.
- Support senior management with departmental goals and delivery
Key responsibilities
- Take ownership of end-to-end project delivery
- Act as the primary liaison with sponsors, investigators, and clinical operations team
- Ensure compliance with GCP, ICH, ISO 14155, and applicable EU/US regulatory frameworks (when required).
- Oversee financial performance, risk management, and resource planning of your clinical studies
- Supervise and support cross-functional project teams.
- Contribute to proposals, bids, and client meetings
About you
We are looking for someone who thrives in a fast-paced, high-accountability environment.
You bring:
- 8+ years of clinical research experience with at least 4+ years in demonstrable project management positions either in a CRO, pharma or biotech environment.
- Minimum of a life sciences degree or equivalent but ideally Masters/PhD.
- Strong knowledge of GCP, ICH, ISO 14155,
- Experience in project and financial management of clinical studies.
- Excellent organisational and communication skills.
- Confidence working independently while nurturing a positive team culture.
- Confident working at pace and managing multiple deliverables.
- Excellent technical skills (Microsoft suite, CTMS, PM tools)
Must have:
- Positive mindset, passion and integrity
- Team spirit and true sense of collaboration
- Drive and a spring in their step
- Can do attitude and a growth mindset
Nice to have:
- Experience in medical devices
- International clinical trial regulation experience
What you will receive
- Competitive salary + 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 & travel incentives
- Professional memberships paid for
- 24/7 confidential Employee Assistance Programme (EAP)
- Wellbeing, ESG, and charity initiatives
- Supportive and collaborative work culture
Why PHARMExcel?
You will be joining a supportive, forward-thinking team that truly values people. With an exciting portfolio, opportunities for growth, and a culture of trust and collaboration-you will be empowered to make an impact from day one.
We do not just deliver trials-we build lasting relationships and strive to raise the bar in clinical research.
Equal Opportunity Statement
PHARMExcel is an equal opportunities employer and does not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, pregnancy or maternity, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability or age. Our ethos is to respect and value people’s differences, and to help everyone achieve and be their best at work as well as in their personal lives so that they feel proud of the part they play in our success. We believe that all decisions about people at work should be based on the individual’s abilities, skills, performance and behaviour and our business requirements. PHARMExcel operates a zero-tolerance policy to any form of discrimination, abuse or harassment.
Ready to make a difference
Apply today and be part of something exceptional at PHARMExcel!
Please note the closing date for 16th March 2026, applications received after this date may not be reviewed.
For further information contact: Jenny Barnett, HR Consultant, [email protected]