Senior Clinical Project Manager
| Location | United Kingdom | 
| Discipline: | Clinical Operations | 
| Job type: | Permanent | 
| Salary: | ££75,000 - £90,000 | 
| Contact name: | Joe Pearce | 
| Contact email: | joe.pearce@rbwconsulting.com | 
| Contact phone: | +44 1293 584 300 | 
| Job ref: | SCPMUK | 
| Published: | about 8 hours ago | 
| Expiry date: | 03 Dec 2025 23:59 | 
Senior Clinical Project Manager – Small Biotech | Rare Diseases
📍 Remote, UK
💼 Clinical Operations
🧬 Phase II/III Trials
🌍 Global Scope
💰 £75,000 - £90,000 (plus benefits)
RBW Consulting is working with a growing biotech company focused on developing treatments for rare and underserved diseases. With a strong commitment to patient outcomes and innovation, this organization is seeking a Senior Clinical Project Manager to lead and manage global clinical trials across multiple regions.
🔍 The Role:
This is a strategic and hands-on position, ideal for someone with deep clinical operations experience and a passion for rare disease research. You’ll be responsible for managing global clinical studies, overseeing internal and external resources, and ensuring high-quality trial delivery.
🧠 Key Responsibilities:
Lead the planning, execution, and oversight of global clinical trials, ensuring alignment with timelines, budgets, and regulatory standards.
Manage relationships with CROs, vendors, and internal stakeholders to ensure smooth trial operations.
Contribute to protocol development, study design, and operational strategy.
Monitor trial progress, identify risks, and implement mitigation strategies.
Support regulatory submissions and interactions as needed.
Ensure compliance with ICH/GCP and local regulatory requirements.
Collaborate cross-functionally with departments such as Regulatory, Medical Affairs, and Quality.
Represent the company at investigator meetings and external engagements.
✅ Ideal Profile:
Life sciences degree (advanced degree preferred).
Significant experience in clinical operations within biotech setting.
Proven track record in managing global clinical trials, ideally in rare or complex disease areas.
Proven ability to develop study-related documents unassisted (such as developing SOPs or contributing to protocols from operational perspective).
🌱 Why Join?
Be part of a mission-driven biotech with a high-impact pipeline.
Influence clinical strategy and contribute to shaping global programs.
Work in a collaborative, science-led culture with strong values.
Competitive compensation and flexible remote working.
To apply:
Please click ‘apply’ or contact Joe Pearce for any further information
About RBW Consulting:
RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.
We are an equal opportunities Recruitment Business and Agency:
RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.
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