Senior Study Coordinator - Clinical Trials & Data Management

Panthera Bio; York and North Yorkshire; Vor Ort; GBP 28.000 - 35.000; Vollzeit

Benefits dieser Stelle

25 days leave

Leave buy/sell

Life insurance

Healthcare cash plan

Employee assistance

Sickness policy

Cycle to work

EV scheme

Zusammenfassung

Panthera Biopartners York is seeking a Study Coordinator 3 to manage clinical trial data and ensure site regulatory compliance. The role covers detailed data entry, documentation tracking, CRA visit prep, and readiness across trial activities at the York Clinical Research Site.

Ideal candidates will be highly organized, data-driven, and experienced in a similar environment, with strong communication across study teams and vendors. Some travel to other Panthera sites may be required.

Qualifikationen

• Experience in clinical trial data management.
• Familiarity with ISF, logs, EDC.
• Ability to support CRA visits and safety reporting.

Aufgaben

• Oversee study trackers, timelines, enrolment and progress.
• Lead day-to-day site management and study readiness.
• Coordinate communication between study teams, vendors, monitors, and site staff.
• Ensure accurate documentation, data entry and regulatory compliance (ISF, logs, EDC).
• Support monitoring activities, CRA visits, and safety reporting.

Kenntnisse

Highly organized

Data driven

Query resolution

Jobbeschreibung

Panthera Biopartners York is seeking a Study Coordinator 3 to manage clinical trial data and ensure site regulatory compliance. The role covers detailed data entry, documentation tracking, CRA visit prep, and readiness across trial activities at the York Clinical Research Site.

Ideal candidates will be highly organized, data-driven, and experienced in a similar environment, with strong communication across study teams and vendors. Some travel to other Panthera sites may be required.