Clinical Data Manager / Data Coordinator
SciPro Cambridge, England, United Kingdom
Clinical Data Manager / Data Coordinator
SciPro are partnered with a growing biotech company developing an innovative new era of cancer diagnostics. They are looking for a Clinical Data Manager/Data Coordinator to support ongoing clinical studies by managing trial data and coordinating with clinical and laboratory teams.
Responsibilities:
* Clean, standardise, and validate clinical trial data.
* Build, manipulate and maintain study databases.
* Ensure data quality and compliance with GCP and data protection standards, and TMF.
* Liaise with and train trial and lab staff for accurate data collection.
* Assist with regulatory submissions and documentation.
* Support training of trial personnel on data processes.
Requirements:
* PhD or MSc in a STEM field (e.g. Bioinformatics, Statistics, Engineering etc).
* Hands-on experience with Electronic Data Capture (EDC) systems. Medidata Rave would be a plus.
* Track record of working with clinical trial data and documentation. Colorectal or Gynae cancer would be a plus.
* Knowledge of GCP and GDPR for clinical data.
* Programming skills (Python, R) and version control (Git).
* Trial site monitoring or coordination experience.
Progressing towards their biggest clinical trial to date and expanding into new areas of oncology, this is a pivotal position where you will make an immediate impact in a purpose-driven environment. With a thriving culture you can expect to develop your scientific programming skills alongside likeminded people.
This is a full-time, permanent role, 3 days a week onsite in South Cambridge.
Seniority level
Associate
Employment type
Full-time
Job function
Science and Information Technology
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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