Study Coordinator — Own & Deliver Clinical Trials

Panthera Biopartners; Rishton; On-site; GBP 33,000 - 39,000; Full time

Benefits offered by this job

25 days annual leave

Life insurance 3x salary

Healthcare cash plan

Employee assistance programme

Electric Car Scheme

Annual Self-Care Day

Job summary

Panthera Biopartners is seeking an experienced Study Coordinator to join our Preston York site. You will take ownership of studies, manage trackers, timelines, enrolment and ensure the smooth delivery of clinical trials while working with clinical teams, monitors, vendors and site colleagues.

The role requires strong organisational skills, meticulous documentation, and a good grasp of regulatory requirements.

Qualifications

• Experience in clinical research or a regulated environment.
• Experience coordinating clinical studies and maintaining study documentation.
• Strong data-entry skills with accuracy and deadlines.
• Understanding of clinical trial documentation and regulatory requirements.

Responsibilities

• Taking ownership of study trackers, timelines, enrolment and overall study progress.
• Leading day-to-day study coordination and ensuring the site is ready for key study activities, including pre-randomisation.
• Coordinating communication between study teams, vendors, monitors and site colleagues.
• Maintaining accurate and timely study documentation, including the ISF, study logs and EDC systems.
• Completing accurate data entry and supporting timely query resolution.
• Preparing for and supporting CRA monitoring visits.
• Supporting safety reporting requirements, including SAEs.
• Helping ensure studies are delivered in line with protocols and site procedures.

Skills

Organised

Attention to detail

Communication skills

Data entry

Tools

EDC systems

Job description

Panthera Biopartners is seeking an experienced Study Coordinator to join our Preston York site. You will take ownership of studies, manage trackers, timelines, enrolment and ensure the smooth delivery of clinical trials while working with clinical teams, monitors, vendors and site colleagues.

The role requires strong organisational skills, meticulous documentation, and a good grasp of regulatory requirements.