Senior Clinical Project Manager

1w1 week ago

Relation Therapeutics

London, GB · Contract · £70,000 – £95,000

About this role

Relation is an end-to-end biotech company developing transformational medicines, leveraging single-cell multi-omics from patient tissue, functional assays, and machine learning to drive disease understanding. We seek an experienced Clinical Project Manager to support execution of future clinical and observational research programmes. This role coordinates internal teams and external partners for efficient, high-standard delivery.

You will work closely with clinical operations, translational science, data science, and external CRO partners to advance the pipeline toward the clinic. Responsibilities include leading day-to-day operational management and ensuring smooth programme delivery. This position helps build operational foundations at an early stage of clinical development.

At the heart of London, our state-of-the-art wet and dry laboratories foster interdisciplinary collaboration. We are rapidly scaling technology and discovery teams amid dual GSK collaborations on fibrosis, osteoarthritis, and our internal osteoporosis programme. Innovation thrives through diversity and inclusive teams where everyone contributes unique perspectives.

Joining Relation offers a chance to shape culture, influence strategic direction, and impact patients' lives. Become part of an exceptionally talented team pushing drug discovery boundaries. Help transform groundbreaking science into impactful therapies.

Requirements

Experience managing clinical or observational studies within biotech, pharma, or CRO environments
Strong project management skills
Familiarity with coordinating clinical operations and translational science teams
Experience working with CRO partners and external vendors
Knowledge of study start-up activities including site feasibility
Ability to track study progress, manage risks, and ensure regulatory compliance
Proficiency in preparing clinical study documentation and plans

Responsibilities

Lead day-to-day operational management of clinical and observational studies
Coordinate timelines, milestones, and deliverables across internal teams and external partners
Support study start-up activities including site identification, feasibility, and vendor selection
Manage CROs, clinical vendors, and academic collaborators
Ensure studies are delivered on time, within scope, and in compliance with regulatory and ethical standards
Track study progress and proactively identify risks and mitigation strategies
Support preparation of study documentation including protocols, study plans, and operational plans
Contribute to the development of scalable clinical operations processes

Benefits

Work in state-of-the-art wet and dry laboratories in central London
Collaborate on GSK partnerships tackling fibrosis, osteoarthritis, and osteoporosis
Join a rapidly scaling innovative TechBio company
Contribute to inclusive teams fostering diversity and interdisciplinary collaboration