Data Compliance Coordinator

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

THE OPPORTUNITY

We have an exciting opportunity for a Data Compliance Coordinator to join our Clinical Research Group (CRG) in Manchester, supporting the management and delivery of UK clinical studies at our Manchester research site.

Reporting to the Manager, Data Compliance, you’ll join a close-knit team responsible for data management and compliance across our clinical research studies.

Acting as an important link between clinical trial sponsors and the research site, you’ll work directly with sponsor representatives while managing study and patient data, maintaining essential documentation and ensuring the quality and integrity of clinical trial information.

This is an excellent opportunity for someone looking to build their career in clinical research and gain valuable experience working across multiple studies in a global scientific organization.

This is a fully onsite position in Manchester, working 37 hours per week.

• Monday–Thursday: 8:00am–4:30pm
• Friday: 8:00am–4:00pm

WHAT YOU WILL DO:

In this role, you will:

Support the management of UK clinical studies conducted through our Manchester site

Act as a key operational link between clinical trial sponsors and the research site

Work directly with sponsor representatives and clinical research stakeholders

Manage and maintain accurate clinical study and patient data

Complete electronic Case Report Form (eCRF) data entry and resolve data queries

Maintain Investigator Site Files (ISF) and other essential study documentation

Coordinate data management and compliance activities across multiple studies

Prepare for monitoring visits and support timely follow-up actions

Help ensure study activities meet ICH/GCP, regulatory and data protection requirements

Perform quality checks to maintain high standards of data accuracy, completeness and integrity

Collaborate with colleagues across the site to support an efficient and positive clinical trial experience for participants

REQUIREMENTS:

Minimum 1 year of relevant experience in clinical research, data management, or related field

Technical certification may be required for certain positions

Strong knowledge of ICH/GCP guidelines and regulatory requirements

Proficient in electronic Case Report Form (eCRF) data entry and query resolution

Experience maintaining Investigator Site Files (ISF) and study documentation

Excellent attention to detail and quality control capabilities

Strong time management skills with ability to handle multiple studies simultaneously

Proficiency in Microsoft Office applications

Ability to learn and apply medical terminology

Strong verbal and written communication skills in English

Ability to work both independently and collaboratively in a team environment

Experience with monitoring visit preparation and follow-up

Knowledge of data protection regulations and compliance requirements

Physical ability to be stationary for extended periods and perform computer work

Ability to travel occasionally as needed