At PHARMExcel, we are a team driven by integrity, collaboration, and a genuine passion for clinical research. As an ISO 9001certified, organisation, we pride ourselves in delivering high-quality, client focused clinical services. 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. With our diverse pipeline of work, we are now looking for an exceptional l Senior Clinical Study Project Manager (CSPM) to join our expanding team.
The Role
As a Senior CSPM at PHARMExcel, you will take key responsibility for the execution and delivery of your client’s programme of work. Whether it is an ATMP, CTIMP, non-interventional or medical device clinical investigation, you will be the driving force behind your studies.
You will be the main point of contact for our clients and clinical operations team, ensuring integrity, compliance, and excellence in every phase of trial delivery.
You will be a leader and a driver and not scared of challenging the status quo. You will be confident and knowledgeable, building trust with your clients by guiding and supporting them.
We are looking for someone with a positive mindset and passion
You will be part of a 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!
You will:
- Be responsible and accountable for o your clinical studies and investigations
- Be a role model and mentor, guiding junior team members with clinical expertise and confidence.
- 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 and brings:
- 5+ years of clinical research experience in a CRO, pharma company, or CTU.
- A life sciences degree or equivalent.
- Proven clinical project and study management
- 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.
Must Have
- Passion and Integrity
- Integrity and Team Spirit
- Drive and a Spring in their step!
Nice to Have
- Experienced in medical devices
- International clinical trial regulation experience
What You will Get
- Competitive salary
- Generous annual leave + your birthday off
- Private medical insurance
- Company bonus (performance-based)
- 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 now or get in touch with our People Team!
careers@pharmexcel-cro.com
Contact: Dani Harrison, Head of People & Culture – dani.harrison@pharmexcel-cro.com