Study Director

VRS-UK

Cambridge

On-site

GBP 65,000 - 90,000

Full time

8 days ago

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Job summary

VRS-UK is seeking an experienced Study Director to lead regulated bioanalytical projects in a renowned biopharmaceutical lab. You will oversee PK, ADA and biomarker studies and serve as the scientific contact for internal teams and external clients.

The ideal candidate has a BSc/MSc in Biology or related field, hands‑on bioanalytical expertise, and proven GCP/GLP experience. Training is provided for complementary skills, with a strong focus on quality and regulatory compliance.

Qualifications

  • Degree in biology or related field (BSc/MSc).
  • Specialist knowledge of bioanalytical techniques in PK/ADA/biomarker studies.
  • Experience with GCP and GLP; managing regulated studies.
  • Excellent written and verbal communication; scientific contact for teams/clients.
  • Strong work ethic and willingness to learn; training provided for complementary skills.

Responsibilities

  • Oversee, manage and provide strategic direction for regulated studies.
  • Lead PK, ADA and biomarker studies to meet scientific and regulatory standards.
  • Act as scientific contact for internal teams and external clients.
  • Ensure delivery of high-quality data and compliant study execution.

Skills

Analytical mindset
Communication skills
Work ethic

Education

BSc/MSc in Biology or related field

Job description

Exciting new opportunity for an experienced and analytically minded Study Director seeking career progression with an internationally renowned and expanding Biopharmaceutical Laboratory!

In this diverse, multifaceted position, you will call upon your expertise in regulated studies to undertake a broad range of challenging bioanalytical projects for several world-leading organisations. Acting as a scientific point of contact for both internal teams and external clients, your work will focus on the oversight, management, and strategic direction of studies supporting PK, ADA and biomarker analysis, ensuring delivery to the highest scientific and regulatory standards.

The ideal candidate will have:
  • A relevant degree (BSc/MSc in Biology or related field)
  • Specialist knowledge & experience in bioanalytical techniques, particularly within PK, Anti-drug Antibody (ADA) & Biomarker studies
  • Proven experience working to GCP and GLP regulations, including managing and directing regulated studies
  • Excellent written and verbal communication skills, with the ability to act as a scientific point of contact
  • Strong work ethic and drive to learn
  • Candidates with strong experience in either regulated work or biological work are encouraged to apply, as training can be provided for the complementary skill set

This is an excellent opportunity to join a respected organisation, where scientific quality, collaboration, and professional development are genuinely valued.

Keywords: Project Manager, Study Director, Regulated studies, biology, Biopharmaceuticals, biotherapeutics, immunoassay, ELISA, bioanalysis, analysis, analytical, anti-drug, immunoaffinity, GLP, GCP, protein, peptide, antibodies, enzyme immunoassay, Gyrolab, MSD, Mesoscale Discovery, Cambridgeshire, Cambridge, Suffolk, East Anglia, Cambridge, Cambridgeshire, VRS9519PC

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