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:

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

Essential:

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

Knowledge of cancer development and genetics.
Experience in clinical trial management or monitoring.
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