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Clinical Research Project Manager (Part-Time, Maternity Cover)

Mitra Bio
London

Apply Now

Job details

Part-time | Fixed term contract

Qualifications

Clinical research

Full job description

Competitive
London

May 14, 2026

Company description

Mitra Bio is building the future of skincare through cutting-edge science and technology. Backed by Khosla Ventures, Illumina, and Innovate UK, we help people better understand their skin over time using simple, non-invasive skin sampling and advanced data analysis. Our goal is to make highly personalised skincare more effective, accessible, and science-driven.

Role description

We’re looking for a highly organised, proactive, and experienced Part-Time Clinical Research Project Manager to join us on a 12-month fixed-term maternity cover contract supporting one of Mitra Bio’s core clinical studies.

This role is ideal for someone who enjoys bringing structure to complexity, thrives in fast-moving environments, and is confident operating independently. You’ll play a critical role in ensuring the successful delivery of a multi-centre molecular diagnostics clinical study, acting as the central coordination point across clinical sites, vendors, investigators, and internal teams.

You’ll report into the Head of Market Access / CEO and work closely with both internal and external stakeholders to ensure study timelines, regulatory submissions, budgets, and operational delivery remain on track. This is a hands-on role with real ownership and visibility across the business.

Contract details

12-month fixed-term contract (maternity cover)
July 2026 – June 2027
Part-time: 16 hours per week

What you’ll own

Day-to-day coordination and delivery of a multi-centre molecular diagnostics clinical study
Management of study timelines, recruitment targets, and operational milestones across participating sites
Oversight of protocol amendments, ethics submissions, and Trial Master File (TMF) management
Study budget tracking, vendor coordination, and reconciliation of site payments and invoices
Ensuring study activities remain compliant with GCP, IVDR, and regulatory requirements
Facilitating communication and accountability across investigators, vendors, clinical sites, and internal teams

What we’re looking for

3+ years of experience managing clinical trials or clinical research projects
Experience coordinating international or multi-centre clinical studies
Comfortable operating independently and proactively solving problems
Hands-on experience with ethics committee submissions and protocol amendments
A strong understanding of Good Clinical Practice (GCP) and clinical trial operations
Highly organised, detail-oriented, and able to manage multiple moving pieces simultaneously
Communicate clearly and confidently with both scientific and operational stakeholders
Comfortable working in fast-moving startup or evolving environments
Experience in molecular diagnostics, genomics, or next-generation sequencing workflows
Experience supporting grants or clinical evidence generation projects

We’re particularly interested in hearing from people who are proactive, pragmatic, and excited about cutting-edge clinical research in a fast-moving environment.

Must haves

Based in or near London and available to work in-person with the team on a hybrid basis
Diagnostics or medtech experience
Experience managing clinical study operations and timelines independently
Comfortable working cross-functionally with external sites, vendors, and internal stakeholders
Willingness to travel internationally if required

Nice to haves

Prior startup, biotech experience
Familiarity with regulatory affairs processes
Experience with grants, clinical evidence generation, or translational research projects

What we offer

Flexible part-time working arrangements
High ownership and direct impact on a business-critical clinical programme
The opportunity to work at the intersection of science, diagnostics, and consumer health
A collaborative, ambitious team of scientists, engineers, and operators building something genuinely new
Strong in-person/hybrid culture, fast feedback loops, and minimal bureaucracy
Backing from world-class investors and experienced founders
The opportunity to contribute to the future of personalised skincare and longevity science

Interview process

30 minute screen with Talent Acquisition
1 hour interview with Head of Market Access and Scientific Operations Manager
Final conversation with CEO

Diversity, Equity & Inclusion

At Mitra Bio, we believe the best ideas, products, and breakthroughs come from diverse perspectives and lived experiences. We are committed to building an inclusive environment where people feel respected, supported, and empowered to do their best work.

We welcome applicants of all backgrounds, identities, experiences, and ways of thinking, including those who may not meet every qualification listed in the job description. If you’re excited about the role and believe you could make an impact, we’d love to hear from you.

We are committed to creating a fair and accessible hiring process and building a team that reflects the diverse communities we serve.

Apply Now

Refine Your Search

biotech ceo jobs

Clinical Research Project Manager (Part-Time, Maternity Cover)

Solutions Engineer

Chief Development Officer

VP Product

Functional Genomics Scientist

Head of Functional Genomics

Protein Scientist

Head of Product

Head of Majors, Customer Success

Senior Manager - UKI Medical Technology Practice

Sr. Commercial Business Development Manager

PR & Communications Manager

Finance Manager

Executive Assistant

AI Engineering Lead

VP, Business Development

Chemistry Principal Scientist

Community Manager

Talent Acquisition Specialist

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