Clinical Research Associate

Barrington James
Southampton
6 months ago
Applications closed

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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.

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