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Clinical Data Manager / Data Coordinator

JR United Kingdom

Cambridge

On-site

GBP 40,000 - 80,000

Full time

3 days ago

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An innovative biotech company is seeking a Clinical Data Manager/Data Coordinator to play a crucial role in their clinical studies. This position involves managing trial data, ensuring compliance with GCP and GDPR standards, and collaborating with clinical and laboratory teams. As part of a dynamic and purpose-driven environment, you will have the opportunity to enhance your skills while contributing to groundbreaking cancer diagnostics. This full-time role requires a strong educational background in STEM and hands-on experience with clinical data management, making it an exciting opportunity for those passionate about advancing healthcare.

PhD or MSc in a STEM field required.
Experience with EDC systems and clinical trial data management.

Clean, standardise, and validate clinical trial data.
Build and maintain study databases, ensuring compliance.

Clinical trial data management

Data cleaning and validation

Programming skills (Python, R)

Version control (Git)

Knowledge of GCP and GDPR

Trial site monitoring

PhD in a STEM field

MSc in a STEM field

Electronic Data Capture (EDC) systems

Medidata Rave

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Clinical Data Manager / Data Coordinator, Cambridge

Client:

SciPro

Location:

Cambridge, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

Posted:

24.04.2025

Expiry Date:

08.06.2025

Job Description:

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.

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