Global CRA: Site Leadership & Monitoring

Panthera Bio; Lunds kommun; On-site; GBP 42,000 - 64,000; Full time

Job summary

TFS HealthScience is seeking a Clinical Research Associate (CRA) to support clinical trials across designated sites. You will ensure patient safety, data quality, protocol compliance, and strong site performance while managing site activities and building relationships with investigators and staff.

The role requires a Bachelor's degree in Life Sciences and 3-4 years of CRA experience within pharma/biotech/CRO.

Qualifications

• 3-4 years of Clinical Research Associate experience within the pharmaceutical, biotechnology, or CRO industry.
• Strong organizational, communication, and stakeholder management skills.
• Demonstrated ability to work independently and take ownership of site activities and deliverables.
• Solid understanding of ICH-GCP, clinical trial processes, and applicable regulations.
• Oncology and/or Phase I clinical trial experience is preferred but not essential.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, ICH-GCP, and applicable regulations
• Ensure subject safety, data integrity, and protocol compliance throughout the study lifecycle
• Build and maintain strong relationships with investigators, study coordinators, and site personnel
• Identify, document, and proactively resolve site issues, risks, and recruitment challenges
• Complete monitoring reports and maintain accurate study documentation and trial management systems
• Collaborate with project teams and stakeholders to ensure study milestones and deliverables are achieved

Skills

Independent work

Stakeholder management

ICH-GCP knowledge

Data quality focus

Education

Bachelor's degree in Life Sciences or related field

Job description

TFS HealthScience is seeking a Clinical Research Associate (CRA) to support clinical trials across designated sites. You will ensure patient safety, data quality, protocol compliance, and strong site performance while managing site activities and building relationships with investigators and staff.

The role requires a Bachelor's degree in Life Sciences and 3-4 years of CRA experience within pharma/biotech/CRO.