At a Glance
- Tasks: Manage and coordinate early-phase clinical studies in a fast-paced biotech environment.
- Company: Innovative biotechnology company focused on developing precision medicines for serious diseases.
- Benefits: Collaborative culture, opportunity to work with industry leaders, and career growth potential.
- Other info: Join a dynamic team dedicated to transforming healthcare through innovative solutions.
- Why this job: Make a real impact in advancing cutting-edge therapies while gaining valuable experience.
- Qualifications: Experience in clinical trials, strong organisational skills, and ability to work across teams.
The predicted salary is between 55000 - 65000 £ per year.
We're working with an innovative clinical-stage biotechnology company developing next-generation precision medicines for serious diseases with significant unmet need. Leveraging advanced platform technologies and a highly collaborative scientific approach, the company is advancing a growing pipeline of early clinical and translational programmes.
Following recent progression into clinical development, the organisation is entering an exciting phase of growth and is expanding its operational capabilities to support ongoing and future clinical studies globally. The company offers a fast-paced, collaborative, and science-driven environment with the opportunity to work across cutting-edge therapeutic programmes alongside experienced industry leaders.
We are seeking an experienced and highly organised Clinical Project Manager to support the delivery of early-phase clinical programmes across a growing pipeline. This individual will play a central role in the operational management and cross-functional coordination of Phase 1/2 clinical studies, working closely with internal teams, CROs, vendors, and external partners to ensure high-quality and timely execution of clinical development activities.
The ideal candidate will bring strong operational oversight experience within biotech or CRO environments, alongside the ability to operate effectively within a lean and fast-moving organisation.
- Clinical Trial Delivery & Oversight
- Support the planning, execution, and oversight of Phase 1/2 clinical studies across multiple programmes
- Track study timelines, milestones, risks, and deliverables to ensure successful study execution
- Ensure studies are conducted in compliance with protocol, GCP, SOPs, and regulatory requirements
- Monitor vendor performance, timelines, quality metrics, and study deliverables
- Support issue escalation, risk mitigation, and resolution of operational challenges
- Cross-Functional Project Coordination
- Coordinate activities across Clinical Operations, Clinical Development, Regulatory, Translational Medicine, Biomarkers, Data Management, Biostatistics, Safety, and CMC teams
- Support preparation and maintenance of study plans, governance materials, and project trackers
- Prepare operational updates, study status reports, and risk assessments for internal leadership
- Support inspection readiness and maintenance of audit-ready documentation
- Contribute to building scalable clinical operations infrastructure within a growing biotech environment
- Support study start-up planning for future pipeline programmes
- Assist with feasibility assessments, study planning, and operational strategy discussions
Qualifications:
- Early-phase biotech experience
- Experience supporting global or multi-regional clinical studies
- Proven experience managing or coordinating clinical trials within biotech, pharma, or CRO environments
- Strong understanding of Phase 1/2 clinical trial operations
- Excellent organisational, communication, and project management skills
- Comfortable operating across scientific and operational teams
Clinical Trials Project Manager in City of London employer: Hlx Life Sciences
Join an innovative clinical-stage biotechnology company that is at the forefront of developing next-generation precision medicines. With a fast-paced, collaborative work culture and a commitment to employee growth, you will have the opportunity to work alongside industry leaders on cutting-edge therapeutic programmes. This role not only offers the chance to make a meaningful impact in the field of medicine but also provides a supportive environment for professional development and operational excellence.
