At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.

Do you have a data entry/quality compliance background?

Interested in the dynamic clinical research industry?

We are currently looking to recruit a Data Compliance Coordinator for our clinical site in Hexham, United Kingdom.

Working 37 hours a week, Monday to Friday, this role will be responsible for oversight of data and quality control to the clinical trial process by ensuring all study documentation and source data is accurate and up to date.

Key responsibilities for a Data Compliance Coordinator are as follows:

• Coordinates operational compliance activities on one or more studies to ensure successful delivery of the studies.
• Ensures accurate and timely entry of all data in the CRF from the source notes, and tracks the flow of the CRF’s, queries, and patient recruitment statuses; reports out the flow of data.
• Maintains ISF and study trackers as delegated.
• Follows the QC process and checks that ICF’s are correctly completed.
• Ensures that protocol visit windows are scheduled according to the protocol requirements and reports deviations.
• QCs all supporting reports (laboratory reports/GP SDV/Consultant) to ensure they are reviewed and signed off by a physician within the appropriate timelines and flags any out of range values.
• Assist with archiving procedures if required.
• Assists monitors, sponsor representatives with the preparation of monitoring visits and query resolutions during monitoring visits.
• Identifies quality issues (QI) and to reports them, and applies CAPA reporting and root cause analyses.
• Prepares and collates regulatory documents for submission.
• Interprets and adheres to company SOP and COP, and assists with input during the review process.
• Adheres to the rules and regulations of ICH, GCP and other regulatory and ethical guidelines and data protection regulations.
• Assists with drafting compliance reports.