Hybrid Site Readiness Lead - Clinical Trials Operations

Panthera Clinic; Preston; Hybrid; GBP 35,000 - 40,000; Full time

Benefits offered by this job

25 days’ annual leave

Annual Leave Buy and Sell

Life insurance 3x salary

Healthcare cash plan

Employee Assistance Programme

Enhanced sickness & family policies

Electric Car Scheme

Annual Self-Care Day

Job summary

Panthera Biopartners Ltd is seeking a Site Readiness Specialist to join our Head Office team in Fulwood on a hybrid basis. You will drive operational readiness and study start-up activities to enable site activation and successful study execution.

You will collaborate with project teams, external vendors and site operations to ensure regulatory, quality and safety standards are maintained across multiple studies.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Experience in clinical operations, study start-up, or site management.

Responsibilities

• Drive operational readiness for new studies and study start-up documentation.
• Develop study-specific start-up documents to ensure sites meet regulatory, quality and operational requirements.
• Coordinate with project managers to align site readiness with timelines and risk strategies.
• Maintain site readiness checklists, mock visits, and training records; report progress to PM.
• Ensure facilities, equipment, labs and services align with protocol requirements before activation.
• Assist in health and safety reviews and risk assessments for new studies.
• Support external vendors and act as operational liaison between sites and project teams.
• Contribute to training material development and site training strategies.

Skills

Clinical ops

Study start-up

Site management

ICH GCP

Inspection readiness

Education

Bachelor’s degree in life sciences

Job description

Panthera Biopartners Ltd is seeking a Site Readiness Specialist to join our Head Office team in Fulwood on a hybrid basis. You will drive operational readiness and study start-up activities to enable site activation and successful study execution.

You will collaborate with project teams, external vendors and site operations to ensure regulatory, quality and safety standards are maintained across multiple studies.