Clinical Research Associate

Barrington James; England; Hybrid; GBP 60,000 - 80,000; Part time

Job summary

A leading clinical research firm is looking for a Freelance Clinical Research Associate at the Associate Level, focusing on oncology clinical trials. This hybrid role is ideal for those early in their career who seek hands-on experience and involvement in site monitoring and compliance with regulatory guidelines. The candidate should have a relevant bachelor’s degree and 1–2 years of clinical research experience.

Qualifications

• 1–2 years of clinical research experience, internships or study coordinator experience included.
• Exposure to oncology trials (academic, site, or CRO experience).
• Understanding of ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Conduct site monitoring visits for oncology clinical trials.
• Assist in site selection and feasibility assessments.
• Ensure proper documentation and resolution of site issues.

Skills

Organizational skills

Communication skills

Interpersonal skills

Detail-oriented

Proficiency in Microsoft Office

Education

Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or related field

Tools

Clinical trial management systems (CTMS)

Electronic Data Capture (EDC) systems

Job description

Job Title: Freelance Clinical Research Associate – Associate Level (Oncology)

Location: Hybrid UK Based

Employment Type: Freelance

Function: Clinical Operations

Therapeutic Area: Oncology

Reports To: Clinical Operations Manager

About the Role

We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. This is an exciting opportunity for an early-career CRA to gain hands-on experience in a dynamic, cross-functional research environment. You will support clinical trial activities across multiple oncology study sites, ensuring compliance with regulatory guidelines, ICH-GCP, and study protocols.

Key Responsibilities

• Conduct site monitoring visits (pre-study, initiation, routine, and close-out) for oncology clinical trials in accordance with study protocols and regulatory requirements.
• Assist in site selection and feasibility assessments.
• Ensure proper documentation and timely resolution of site issues.
• Support site staff in understanding and complying with study protocols and GCP guidelines.
• Verify source data and case report forms (CRFs) for accuracy, completeness, and consistency.
• Ensure timely collection and review of essential regulatory documents.
• Track patient recruitment and retention efforts at assigned sites.
• Participate in CRA training sessions, project team meetings, and sponsor meetings as required.
• Maintain high-quality communication with clinical sites and sponsor/CRO teams.
• Escalate site performance or compliance issues as needed.

Required Qualifications

• Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered).
• Exposure to oncology trials (academic, site, or CRO experience).
• Understanding of ICH-GCP guidelines and regulatory requirements.
• Strong organizational skills with attention to detail.
• Ability to manage multiple tasks and priorities independently.
• Excellent communication and interpersonal skills.
• Proficiency with clinical trial management systems (CTMS), EDC systems, and Microsoft Office.