Senior Clinical Research Associate (UK)

Theradex Oncology; Greater London; On-site; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Competitive compensation

Opportunities for growth

Friendly, supportive culture

Job summary

A biotechnology company is looking for a Senior Clinical Research Associate based in London. In this full-time role, you will oversee site management and monitoring across clinical trials. Ideal candidates will have a Bachelor's degree in a relevant field and at least 5 years of experience managing clinical trial sites, particularly in early-phase oncology studies. The position involves domestic and international travel approximately 70% of the time and offers a supportive work culture with competitive compensation.

Qualifications

• 5+ years' experience as a Clinical Research Associate.
• Proven track record managing clinical trial sites.
• Experience in monitoring early-phase oncology studies.

Responsibilities

• Perform site management and monitoring activities during all phases of clinical trials.
• Ensure compliance with sponsor protocols and industry standards.
• Collaborate with site staff to solve operational issues.
• Document site visits, adverse events, and study progress.
• Provide training and mentorship to junior staff.

Skills

Clinical trial site management

Monitoring oncology studies

Regulatory compliance

Training and mentorship

Education

Bachelor's degree in biological or science-related field

Job description

Senior Clinical Research Associate (UK)

Theradex Oncology

Location: London, England, United Kingdom

About the role

The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle on behalf of multiple sponsors. We seek an experienced onsite monitor to join our skilled CRAs team.

Key Responsibilities

• Perform site management and monitoring activities during all phases of clinical trials.
• Ensure compliance with sponsor protocols, regulatory requirements, and industry standards.
• Collaborate with site staff, sponsors, and CROs to solve operational issues.
• Document and report site visits, adverse events, and study progress.
• Provide site training and mentorship to junior staff.

Requirements

• Bachelor's degree (BSc, BA, or RN equivalence) in biological or science‑related field or equivalent experience.
• At least 5 years’ experience as a Clinical Research Associate with proven track record managing clinical trial sites.
• Experience in monitoring oncology early‑phase I‑III studies.

Additional Requirements

• Ability to travel approximately 70% of the time (domestic and/or international) with potential overnight stays.
• Valid driver’s licence and passport preferred.
• Willingness to pass background clearance checks, which may be run periodically.

What we offer

Friendly, supportive culture that puts people first, competitive compensation, and opportunities for growth.

Equal Opportunity Statement

Theradex is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment.

Job Details

• Seniority level: Mid‑Senior
• Employment type: Full‑time
• Job function: Research
• Industries: Biotechnology Research and Pharmaceutical Manufacturing