Job Description
About the Company:\n\nWe 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.\n\nAbout the Role:\n\nWe 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.\n\nKey Responsibilities:\n\nClean, standardise, and prepare clinical trial data for analysis.\nBuild and manage study databases, ensuring data accuracy and validation.\nRaise data queries and liaise with clinical centres to resolve issues.\nTrain trial personnel to improve data collection quality.\nMaintain Trial Master Files (TMF) and ensure compliance with GCP and ICH regulations.\nSupport regulatory teams with data for reports (e.g., Annual Progress Reports).\nSkills & Qualifications:\n\nEssential:\n\nPhD or Master’s degree in a STEM subject (e.g., Bioinformatics, Genetics, Statistics, Computer Sciences).\nExperience with Electronic Data Capture (EDC) systems and clinical trial documentation.\nStrong understanding of data management best practices and regulatory requirements (GCP & UK GDPR).\nExcellent communication skills to present actionable insights.Desirable:\n\nKnowledge of cancer development and genetics.\nExperience in clinical trial management or monitoring.\nProficiency in scientific programming (Python, R) and version control (Git).Why Apply?\n\nJoin a mission-driven company making a real impact in healthcare.\nWork in a collaborative, innovative environment at the forefront of biotechnology.\nCompetitive salary and benefits package