Data Compliance Coordinator Manchester, United Kingdom

Meeveem Limited; Manchester; Hybrid; GBP 28,000 - 38,000; Full time

Job summary

Thermo Fisher Scientific in Manchester is seeking a Data Compliance Coordinator to support UK clinical studies at the local site. You will handle data management, regulatory compliance, and sponsor-site coordination in a fast-paced environment.

The role requires 1 year of clinical research experience, proficiency with eCRF and ISF, and strong English communication. This onsite position offers regular hours and collaboration across a global clinical research team.

Qualifications

• Minimum 1 year of experience in clinical research or data management.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Proficient in eCRF data entry and data query resolution.
• Experience maintaining ISF and study documentation.
• Excellent attention to detail and quality control.
• Strong time management and ability to manage multiple studies.
• Proficiency in Microsoft Office; ability to learn medical terminology.
• Strong English written and verbal communication.
• Ability to travel occasionally.

Responsibilities

• Support the management of UK clinical studies conducted through our Manchester site.
• Act as an 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.

Skills

Attention to detail

Time management

English communication

Education

Clinical Research Certification

Tools

eCRF data entry

ISF management

MS Office

Job description

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:

• 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 applicationsAbility 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