Clinical Study Coordinator - Preston Site: Own & Deliver

Panthera Biopartners; Lancashire; On-site; GBP 27,000 - 39,000; Full time

Benefits offered by this job

Annual leave

Leave buy/sell

Life insurance

Healthcare plan

Employee assistance

Sickness policy

Electric car scheme

Self-care day

Job summary

Panthera Biopartners is seeking a Study Coordinator at our Preston Clinical Research Site. You will take ownership of study trackers, timelines and enrolment, ensuring smooth delivery of trials and readiness for key activities, including pre-randomisation.

The role requires organised, detail-oriented individuals with experience in clinical research, documentation, data entry and strong communication across teams and external partners. Opportunities to support multiple Panthera sites may arise.

Qualifications

• Organised, detail-focused with multi-study responsibility.
• Experience in clinical research or regulated environments.
• Experience coordinating clinical studies and maintaining study documentation.
• Strong data-entry skills with high accuracy and deadlines.
• Understanding of trial documentation and regulatory requirements.
• Strong communication with teams, monitors and external partners.
• Ability to prioritise and keep studies moving forward.

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 activities, including pre-randomisation.
• Coordinating communication between study teams, vendors, monitors and site colleagues.
• Maintaining accurate study documentation, including 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 (SAEs).
• Ensuring studies are delivered in line with protocols and regulatory requirements.

Skills

Organised/Detail-oriented

Clinical research experience

Study coordination

Data entry

Regulatory knowledge

Communication skills

Prioritisation

Job description

Panthera Biopartners is seeking a Study Coordinator at our Preston Clinical Research Site. You will take ownership of study trackers, timelines and enrolment, ensuring smooth delivery of trials and readiness for key activities, including pre-randomisation.

The role requires organised, detail-oriented individuals with experience in clinical research, documentation, data entry and strong communication across teams and external partners. Opportunities to support multiple Panthera sites may arise.