Project Manager in Cheshire

Project Manager in Cheshire

Cheshire Full-Time 49500 - 60500 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead innovative gene therapy projects and collaborate with top scientists.
  • Company: Join a pioneering biotech firm at the forefront of gene editing.
  • Benefits: Competitive salary, private medical insurance, and growth opportunities.
  • Other info: Work in a vibrant life science campus with great amenities.
  • Why this job: Make a real impact in biotech while developing your skills in a dynamic environment.
  • Qualifications: Advanced degree in Life Sciences and extensive project management experience required.

The predicted salary is between 49500 - 60500 £ per year.

Pencil Biosciences is a seed stage biotech company developing the novel Break FreeTM gene editing platform. The proprietary gene editor offers unique platform properties including an unparalleled safety profile with applications in therapeutics, diagnostics, and cell engineering.

Pencil Biosciences is advancing an internal in vivo gene-editing therapeutics programme. We are seeking a highly collaborative Project Manager to play a pivotal role in driving our technology from R&D proof-of-concept into clinical translation. Reporting directly to the CEO and working closely with Research Directors, you will be a central figure across the organization. This position offers exposure to all areas of the business while maintaining a core focus on supporting our R&D teams.

This high-impact, hands-on role requires technical fluency and a dynamic approach. You will balance multiple functional areas, including internal R&D alignment, resource planning, third party technology & service evaluations, and vendor management. You will lead key outsourced workstreams with CROs and CDMOs—encompassing preclinical mouse model studies, reagent sourcing (LNPs, mRNA, ssDNA), and CMC workflows.

Sitting alongside an experienced team of gene editors, molecular biologists, and protein engineers, you will help onboard new processes, optimize workflows, and facilitate cross-functional knowledge transfer. While first-hand laboratory experience in gene editing is preferred, extensive wet-lab background is not required.

You will drive forward such activities as:

  • Project Governance: Maintain operational oversight across all internal projects, tracking progress, milestones, and deliverables alongside research teams.
  • Vendor & Partner Management: Lead engagements with CROs, CDMOs, and CMC partners, overseeing preclinical animal studies and ensuring external projects are delivered on time and within budget.
  • Strategic Operations: Coordinate key company outputs, including IP filing pipelines, board materials, and internal/external technology evaluations.
  • Cross-Functional Collaboration: Partner with wet-lab scientists and computational biologists to maintain clear communication and drive multi-faceted project tracks.

We would like to hear from you if you have:

  • Advanced degree (BSc/MSc/PhD) in Life Sciences with 5–10+ years of project management experience in biotech or pharma.
  • 5+ years in a dedicated PM role managing complex, interwoven internal and external project tracks.
  • Strong technical background in therapeutic development and fluency in scientific terminology.
  • 3+ years of hands-on expertise using professional project management tools.
  • Proven track record managing CROs/CDMOs and holding external partners accountable to timelines and deliverables.
  • Experience supporting in vivo mouse model work for drug discovery and development.
  • Outstanding communication, problem-solving, and interpersonal skills with an ability to thrive in a multidisciplinary, fast-paced environment.
  • Familiarity with vendor vetting, contract negotiation, and implementing service agreements.

Nice to Have:

  • Direct laboratory or operational experience building preclinical data packages for CTA/IND filings.
  • Familiarity with regulatory documentation processes (CTA/IND filings).
  • Background in Cell & Gene Therapy (CGT) products and platforms.
  • Foundational understanding of gene-editing technologies (including therapeutic and bioproduction applications).
  • Practical familiarity with intellectual property.

Pencil Biosciences perks and benefits:

  • Competitive salary
  • Private Medical Insurance
  • Intellectually stimulating working environment
  • An opportunity to learn both business and science
  • Excellent growth opportunities

The positions will appeal to individuals looking for the challenge of building a technology and being able to take it and move it towards a clinic. We are a small team and have a range of specialists, as such we are looking for people to drive the work and independently take charge of key scientific areas.

Location: Our office and lab facilities are located in Alderley Park, Cheshire, an established life science campus south of Manchester in beautiful Cheshire. In addition to the world class laboratory and office facilities, it offers a multitude of recreational amenities including gym, trails, pub, restaurants and cafes.

Project Manager in Cheshire employer: Pencil Biosciences Limited

Pencil Biosciences is an exceptional employer, offering a unique opportunity to work at the forefront of gene therapy innovation in a collaborative and intellectually stimulating environment. Located in Alderley Park, Cheshire, employees benefit from state-of-the-art facilities and a vibrant community with access to recreational amenities, fostering both personal and professional growth. With a focus on employee development and a hands-on approach to project management, this role provides the chance to make a significant impact in advancing groundbreaking therapeutic technologies.

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Contact Details:

Pencil Biosciences Limited Recruitment Team

We think you need these skills to ace Project Manager in Cheshire

Project Management
Technical Fluency
Vendor Management
Cross-Functional Collaboration
Communication Skills
Problem-Solving Skills
Resource Planning