Study Director

VRS Equipment Leasing Limited

Cambridge

On-site

GBP 60,000 - 90,000

Full time

14 hours ago
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Job summary

Study Director role in our Cambridge facility focuses on overseeing regulated bioanalytical projects with PK, ADA and biomarker analyses, ensuring GLP/GCP compliance and top-tier scientific standards. You will guide studies and act as the scientific point of contact for internal teams and external clients, providing strategic direction and oversight.

The ideal candidate holds a BSc or MSc in biology or related field, with proven regulated-study experience and strong communication skills.

Qualifications

  • A relevant degree (BSc/MSc in Biology or related field).
  • Specialist knowledge & experience in PK, 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.

Responsibilities

  • Oversee, manage, and provide strategic direction for PK, ADA and biomarker studies.
  • Serve as scientific point of contact for internal teams and external clients.
  • Ensure delivery to high scientific and regulatory standards.

Skills

Regulated studies experience
Bioanalysis expertise
GCP/GLP knowledge
Scientific communication
Project management

Education

BSc/MSc in Biology or related field

Tools

Gyrolab
MSD
Immunoassay

Job description

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

The experience expected from applicants, as well as additional skills and qualifications needed for this job are listed below.

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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