Clinical Research Project Manager (Part-Time, Maternity Cover) in City of London

Clinical Research Project Manager (Part-Time, Maternity Cover) in City of London

City of London Part-Time 30000 - 40000 € / year (est.) Home office (partial)
Mitra bio

At a Glance

  • Tasks: Coordinate and manage a multi-centre clinical study in molecular diagnostics.
  • Company: Join Mitra Bio, a cutting-edge skincare tech company backed by top investors.
  • Benefits: Flexible part-time hours, high ownership, and direct impact on innovative projects.
  • Other info: Collaborative team culture with opportunities for growth and minimal bureaucracy.
  • Why this job: Be at the forefront of personalised skincare and contribute to groundbreaking research.
  • Qualifications: 3+ years in clinical trials, strong organisational skills, and proactive problem-solving.

The predicted salary is between 30000 - 40000 € per year.

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.

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 both the Head of Market Access and 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
  • Ability to 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
  • Willingness to travel internationally on occasion if required

We’re particularly interested in hearing from people who are proactive, pragmatic, and excited about cutting-edge clinical research in a fast-moving environment. The ideal candidate will be based in or near London and available to work in-person with the team on a hybrid basis.

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 chat with Talent Acquisition
  • 1 hour interview with Head of Market Access and Scientific Operations Manager
  • Final conversation with CEO

How to Apply

Please submit your CV and a short cover letter outlining your relevant clinical research experience and why you’re interested in Mitra Bio.

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

Clinical Research Project Manager (Part-Time, Maternity Cover) in City of London employer: Mitra bio

Mitra Bio is an exceptional employer, offering a dynamic and collaborative work environment where innovation thrives. As a part-time Clinical Research Project Manager, you'll enjoy flexible working arrangements while playing a pivotal role in advancing personalised skincare through cutting-edge science. With strong backing from world-class investors and a culture that values diverse perspectives, you'll have the opportunity to make a meaningful impact in a fast-paced, supportive setting located in or near London.

Mitra bio

Contact Detail:

Mitra bio Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Research Project Manager (Part-Time, Maternity Cover) in City of London

Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.

Tip Number 2

Prepare for those interviews! Research Mitra Bio and understand their mission in skincare and molecular diagnostics. Tailor your answers to show how your experience aligns with their goals and values.

Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or use online platforms to get comfortable with common questions. The more you practice, the more confident you'll feel when it’s time to shine.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the team at Mitra Bio.

We think you need these skills to ace Clinical Research Project Manager (Part-Time, Maternity Cover) in City of London

Clinical Trial Management
Project Coordination
Good Clinical Practice (GCP)
Regulatory Compliance
Budget Management
Vendor Coordination
Ethics Committee Submissions

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your relevant experience in clinical research. We want to see how your skills align with the role, so don’t be shy about showcasing your achievements!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Tell us why you’re excited about Mitra Bio and how your background makes you a perfect fit for this role. Keep it concise but impactful.

Showcase Your Organisational Skills:As a Clinical Research Project Manager, being organised is key. Use your application to demonstrate how you've successfully managed multiple projects or timelines in the past.

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!

How to prepare for a job interview at Mitra bio

Know Your Stuff

Make sure you brush up on your knowledge of Good Clinical Practice (GCP) and the specifics of clinical trial operations. Being able to discuss these topics confidently will show that you're not just familiar with the basics, but that you truly understand the complexities involved in managing clinical studies.

Show Your Organisational Skills

Since this role requires a high level of organisation, prepare examples from your past experiences where you successfully managed multiple moving pieces. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight how your organisational skills led to successful project outcomes.

Communicate Clearly

Practice articulating your thoughts clearly and confidently, especially when discussing technical aspects of clinical research. You’ll need to communicate with both scientific and operational stakeholders, so being able to convey complex information in an understandable way is key.

Be Proactive

Demonstrate your proactive problem-solving abilities by preparing to discuss challenges you've faced in previous roles and how you overcame them. This will show that you can operate independently and thrive in fast-moving environments, which is exactly what Mitra Bio is looking for.