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Data Manager | Cancer Diagnostics | Cambridge

SoCode Limited

Cambridge

On-site

GBP 30,000 - 60,000

20 days ago

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Job summary

An innovative biotechnology start-up in Cambridge is seeking a Data Manager / Clinical Data Coordinator. Join a mission-driven team that is revolutionizing cancer diagnostics through cutting-edge research. This role involves managing clinical trial data, ensuring data quality, and collaborating with clinical and lab teams. You will play a vital role in improving early detection methods and minimizing unnecessary medical procedures. With a focus on regulatory compliance and data management best practices, this position offers an exciting opportunity to contribute to meaningful healthcare advancements in a dynamic and collaborative environment.

Qualifications

  • PhD or Master's degree in a relevant STEM subject is essential.
  • Experience with EDC systems and strong data management skills are crucial.

Responsibilities

  • Manage and prepare clinical trial data for analysis.
  • Ensure compliance with GCP and maintain Trial Master Files.

Skills

Data Management

Communication Skills

Problem-Solving

Clinical Trial Documentation

Regulatory Compliance

Education

PhD in STEM

Master's in STEM

Tools

Electronic Data Capture (EDC)

Python

R

Git

Job description

About the Company:

We are partnering with an innovative biotechnology start-up based in Cambridge. This company is at the forefront of developing minimally invasive cancer diagnostics, using cutting-edge research to improve early detection and reduce unnecessary medical procedures.

About the Role:

We are seeking a Data Manager / Clinical Data Coordinator to join a dynamic team. This role involves managing clinical trial data, ensuring data quality, and supporting trial coordination. You will work closely with clinical and lab teams, adhering to GCP, SOPs, and data security protocols.

Key Responsibilities:

  1. Clean, standardise, and prepare clinical trial data for analysis.
  2. Build and manage study databases, ensuring data accuracy and validation.
  3. Raise data queries and liaise with clinical centres to resolve issues.
  4. Train trial personnel to improve data collection quality.
  5. Maintain Trial Master Files (TMF) and ensure compliance with GCP and ICH regulations.
  6. Support regulatory teams with data for reports (e.g., Annual Progress Reports).

Skills & Qualifications:

Essential:

  1. PhD or Master's degree in a STEM subject (e.g., Bioinformatics, Genetics, Statistics, Computer Sciences).
  2. Experience with Electronic Data Capture (EDC) systems and clinical trial documentation.
  3. Strong understanding of data management best practices and regulatory requirements (GCP & UK GDPR).
  4. Excellent communication skills to present actionable insights.
Desirable:

  1. Knowledge of cancer development and genetics.
  2. Experience in clinical trial management or monitoring.
  3. Proficiency in scientific programming (Python, R) and version control (Git).

Why Apply?

Join a mission-driven company making a real impact in healthcare. Work in a collaborative, innovative environment at the forefront of biotechnology. Competitive salary and benefits package.

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