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    • Proficient in electronic Case Report Form (eCRF) data entry and query resolution.
    • Knowledge of data protection regulations and compliance requirements.
    • View all Thermo Fisher Scientific jobs - Birmingham jobs - Compliance Officer jobs in Birmingham
    • Salary Search: Data Compliance Coordinator salaries in Birmingham
    • See popular questions & answers about Thermo Fisher Scientific
    • These research study duties can include activity tracking, data inputting, clinic preparation support and research documentation maintenance.
    • Verifies site compliance with electronic data capture requirements.
    • Conducts Source Document Review of appropriate site source documents and medical records.
    • Administrative/secretarial experience in a medical setting: 1 year (preferred).
    • The medical administrator plays a key role in ensuring that patients receive…
    • To provide support and advice to the SAS Tutor involved in the management and delivery of postgraduate medical and dental education.
    • (7.5 hour shift per day).
    • Pension - 5% employer contribution based on qualified earnings.
    • VIVUP - Supermarket & High Street Discounts & Employee Assistant…
    • Maintaining strict confidentiality when handling medical and personal information.
    • Confident working with detailed medical records and written information.
    • Data entry of patient information.
    • Code patient data as required on EMIS Web.
    • Processing incoming and outgoing mail.
    • Summarising and digitising patient records.
  • View similar jobs with this employer
    • Have extensive administration experience within a healthcare / medical setting, such as hospitals, GP surgery etc.
    • Completing redactions for SAR requests.
    • The department supports homecare activity across the Trust processing invoices relating to outsourced Homecare services that provide Pharmacy supplies direct to…
    • Confidence working with data, systems and administrative processes.
    • Accurately entering, validating and maintaining participant and scheme data.
    • Tasks may include data entry and audit, preparation, upload, and tracking of materials and/or reporting.
    • They have excellent self-awareness to know when to…
    • Experience with medical terminology and/or within research or clinical settings is desirable.
    • Ability to find, analyze, interpret, summarize, and compile data…
    • Excellent attention to detail, particularly when entering and checking data.
    • Appointment will be subject to standard entry requirements including receipt of two…
    • Undertake a range of administrative duties, including data entry, document processing and scanning.
    • In this vital role, you will be the friendly face and first…

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Job Post Details

Data Compliance Coordinator
Thermo Fisher Scientific
·
3.4
Birmingham B15 2SQ
Full-time
Apply on company site

Job details

Pay information not provided
Full-time
Monday to Friday
Birmingham B15 2SQ

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

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