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.