Clinical Trials Study Coordinator – Ownership & Impact
Panthera Biopartners
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Benefits offered by this job
Job summary
Panthera Biopartners in Preston seeks an experienced Study Coordinator to own studies at our Clinical Research Site, ensuring on-time delivery and meticulous documentation. You will work with clinical teams, monitors, vendors and site colleagues to support high-quality trial delivery.
Experience in clinical research and data management is essential, with strong attention to detail, the ability to juggle multiple tasks, and a commitment to regulatory requirements and timelines.
Qualifications
- Experience working in clinical research or a regulated environment.
- Ability to manage study documentation with accuracy and deadlines.
- Strong data-entry skills and attention to detail.
- Excellent communication and coordination with teams and external partners.
- Ability to prioritise multiple study activities.
Responsibilities
- Take ownership of study trackers, timelines, enrolment and overall progress.
- Lead day-to-day study coordination and ensure site readiness for activities.
- Coordinate communication between study teams, vendors, monitors and site colleagues.
- Maintain accurate study documentation including ISF, logs and EDC systems.
- Complete accurate data entry and support timely query resolution.
- Prepare for and support CRA monitoring visits and safety reporting.
Skills
Job description
Panthera Biopartners in Preston seeks an experienced Study Coordinator to own studies at our Clinical Research Site, ensuring on-time delivery and meticulous documentation. You will work with clinical teams, monitors, vendors and site colleagues to support high-quality trial delivery.
Experience in clinical research and data management is essential, with strong attention to detail, the ability to juggle multiple tasks, and a commitment to regulatory requirements and timelines.
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