Study Manager

Nexus Life Sciences

Cambridge

Presencial

GBP 35.000 - 45.000

Jornada completa

Hace 5 días
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Descripción de la vacante

Nexus Life Sciences in Cambridge seeks a proactive Study Manager to lead end-to-end delivery of regulated studies (GLP/GCP) and to oversee method validation and sample analysis. You will act as the primary client contact, building partnerships and guiding programme progression while ensuring timely, high-quality data and study reports are delivered.

The ideal candidate holds a degree in Biological Sciences, Biochemistry, Immunology, or related field, with GxP laboratory exposure and strong

Formación

  • Degree in Biological Sciences, Biochemistry, Immunology, or related field.
  • Experience in a GxP laboratory (GLP/GCP preferred).
  • Knowledge of immunoassay platforms (ELISA, LBA, MSD) is advantageous.
  • Strong understanding of EMA/FDA bioanalytical validation guidelines.
  • Excellent communication skills with ability to present scientific data clearly.

Responsabilidades

  • Lead end-to-end delivery of regulated studies (GLP/GCP).
  • Make robust scientific decisions aligned with EMA and FDA guidance.
  • Oversee method validation and sample analysis with scientific authority.
  • Act as primary client contact, building strong partnerships and supporting programme progression.
  • Ensure timely delivery of high-quality data and study reports.

Educación

Biological Sciences / Biochemistry / Immunology degree

Herramientas

ELISA
LBA
MSD

Descripción del empleo

Study Manager

Location: Cambridge, England, United Kingdom (On-site)

About the Company

A leading contract research organisation is looking for a skilled scientist or study coordinator to step into the role of study manager and support in the delivery of client drug development studies.The study manager will be someone with good organisation understanding of molecular techniqeus such as ELISA, MSD as well as being experienced working in a regulated environment.

Responsibilities
  • Lead end-to-end delivery of regulated studies (GLP/GCP).
  • Make robust scientific decisions aligned with EMA and FDA guidance.
  • Oversee method validation and sample analysis with scientific authority.
  • Act as primary client contact, building strong partnerships and supporting programme progression.
  • Ensure timely delivery of high-quality data and study reports.
Qualifications
  • Degree in Biological Sciences, Biochemistry, Immunology, or related field.
  • Experience in a GxP laboratory (GLP/GCP preferred).
  • Knowledge of immunoassay platforms (e.g. ELISA, LBA, MSD) is advantageous.
  • Strong understanding of EMA/FDA bioanalytical validation guidelines.
  • Excellent communication skills with ability to present scientific data clearly.
Pay range and compensation package

Salary - (£35,000 to £45,000 DOE)

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