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

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

London Part-Time 30000 - 40000 € / year (est.) Home office (partial)
Mitra Bio Ltd

At a Glance

  • Tasks: Coordinate and manage a multi-centre clinical study in skincare innovation.
  • 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 clinical programmes.
  • 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. 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 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.

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:

  • 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

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.

Clinical Research Project Manager (Part-Time, Maternity Cover) in London employer: Mitra Bio Ltd

Mitra Bio is an exceptional employer, offering a dynamic and collaborative work culture that thrives on innovation in the skincare industry. With flexible part-time arrangements and a strong emphasis on employee growth, you will have the opportunity to make a significant impact on cutting-edge clinical research while working alongside a passionate team in London. Our commitment to diversity, equity, and inclusion ensures that every voice is valued, making it a truly rewarding place to advance your career.

Mitra Bio Ltd

Contact Detail:

Mitra Bio Ltd Recruiting Team

StudySmarter Expert Advice🤫

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

Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those who might know someone at Mitra Bio. A friendly chat can sometimes lead to opportunities that aren’t even advertised.

Tip Number 2

Prepare for your interviews by researching Mitra Bio and their projects. Show us you’re genuinely interested in personalised skincare and how your experience aligns with their mission. Tailor your answers to reflect their values and goals.

Tip Number 3

Practice your problem-solving skills! Since this role requires independent thinking, be ready to discuss how you've tackled challenges in past projects. We want to see your proactive approach in action!

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re serious about joining our team at Mitra Bio.

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

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

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your experience in managing clinical trials and coordinating multi-centre studies. We want to see how your skills align with the role, so don’t be shy about showcasing your relevant achievements!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re excited about the role at Mitra Bio and how your proactive approach can contribute to our mission. Keep it concise but impactful!

Showcase Your Organisational Skills:Since this role requires a high level of organisation, give examples in your application that demonstrate your ability to manage multiple tasks and timelines effectively. We love seeing how you bring structure to complexity!

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!

How to prepare for a job interview at Mitra Bio Ltd

Know Your Stuff

Make sure you brush up on your knowledge of clinical trials, especially in molecular diagnostics. Familiarise yourself with Good Clinical Practice (GCP) and any relevant regulations. This will not only help you answer questions confidently but also show that you're genuinely interested in the role.

Show Your Organisational Skills

Since this role requires a high level of organisation, be prepared to discuss how you've managed multiple projects or timelines in the past. Bring examples of how you've successfully coordinated teams or handled complex situations, as this will demonstrate your ability to thrive in a fast-moving environment.

Communicate Clearly

Practice articulating your thoughts clearly and concisely. You’ll need to communicate with various stakeholders, so being able to convey complex information simply is key. Consider doing mock interviews with a friend to refine your communication style.

Be Proactive

During the interview, highlight instances where you've taken initiative or solved problems independently. Mitra Bio values proactive individuals, so sharing specific examples of how you've navigated challenges will resonate well with the interviewers.