Clinical Trials Study Coordinator II-II-Data Driven Site Lead

Panthera Biopartners; Greater London; On-site; GBP 27,000 - 33,000; Full time

Benefits offered by this job

25 days annual leave

Life insurance

Healthcare cash plan

Employee assistance programme

Annual Self Care Day

Cycle to Work Scheme

EV Scheme

Annual Leave Buy and Sell

Job summary

Panthera Biopartners in Enfield, England, invites applications for Patient Study Coordinator 2 to join our clinical research site. You will manage trial data, support regulatory compliance, and ensure study readiness through meticulous documentation and trackers.

This role requires strong organisation, precise data entry, and collaboration with study teams, monitors, and vendors. Prior experience in healthcare or CRO settings is desirable, and flexibility to work across Panthera sites may be

Qualifications

• Experience in data management within clinical trials or healthcare settings.
• Familiarity with ISF, logs, EDC and regulatory documentation.
• Able to work across busy site environments with attention to detail.

Responsibilities

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

Skills

Data entry

Regulatory awareness

Organised

Query resolution

Job description

Panthera Biopartners in Enfield, England, invites applications for Patient Study Coordinator 2 to join our clinical research site. You will manage trial data, support regulatory compliance, and ensure study readiness through meticulous documentation and trackers.

This role requires strong organisation, precise data entry, and collaboration with study teams, monitors, and vendors. Prior experience in healthcare or CRO settings is desirable, and flexibility to work across Panthera sites may be