Data Compliance Coordinator
Birmingham, United Kingdom
- Pay
- Pay not listed
- Work setting
- Not stated
- Employment
- Not stated
What you’ll work on
Full postingIn this role, you'll ensure data quality and regulatory compliance while contributing to meaningful clinical research that improves health outcomes.
From the employer’s posting
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. DESCRIPTION: Join our team at Thermo Fisher Scientific as a Corporate Compliance Associate II supporting clinical trials across our research sites. In this role, you'll ensure data quality and regulatory compliance while contributing to meaningful clinical research that improves health outcomes. You'll coordinate operational compliance activities across multiple studies, maintain critical documentation, and work closely with monitors and sponsor representatives to uphold the highest standards of data integrity. As part of our clinical research portfolio, you'll play an essential role in optimizing participant experiences in clinical trials and enabling life-changing therapies to reach those who need them. 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 • Bilingual skills may be required for specific positions • 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
Posting record
Report an error- Status in our records
- Live
- First seen by us
- Oct 21, 2026 · 8 days ago
- Recorded sightings
- 30
- Last seen by us
- Oct 30, 2026
- Reposted
- once since Aug 11, 2026
These dates show when we found the posting. Check the employer’s website to confirm it is still accepting applications. We count a repost when the same title and location comes back as a new listing within 60 days of the last one coming down. Some hiring systems expire listings on a schedule, so repost rates vary by system.
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Job description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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.DESCRIPTION:
Join our team at Thermo Fisher Scientific as a Corporate Compliance Associate II supporting clinical trials across our research sites. In this role, you'll ensure data quality and regulatory compliance while contributing to meaningful clinical research that improves health outcomes. You'll coordinate operational compliance activities across multiple studies, maintain critical documentation, and work closely with monitors and sponsor representatives to uphold the highest standards of data integrity. As part of our clinical research portfolio, you'll play an essential role in optimizing participant experiences in clinical trials and enabling life-changing therapies to reach those who need them.
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
• Bilingual skills may be required for specific positions
• 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
Source details
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- Pay
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- Location & working pattern
Birmingham, United Kingdom
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