Data coordinator Work, Jobs in Birmingham, Wmd (with Salaries)

Data Compliance Coordinator
Thermo Fisher Scientific —Birmingham
- Full-time
- Computer literacy
- English
- Quality control
Contracts & Data Coordinator
Community Housing —Kidderminster
- £34,653 a year
- Full-time
- Microsoft Excel
- Customer service
- Data analysis skills
- Free parking
- Store discount
Quick apply
1d
Data Coordinator
Orbit Group —Stratford-upon-Avon
- £25,422 - £27,964 a year
- Computer skills
- Leadership
3d

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Data Compliance Coordinator

Thermo Fisher Scientific -
Birmingham

Apply Now

Job details

Full-time

Qualifications

Clinical research
Computer literacy
English
Microsoft Office Suite
Quality control
Data entry
Good Clinical Practice (GCP)
Medical terminology
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
Time management

Full 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.

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

Apply Now

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