Clinical Research Associate - Oncology
Reading, England, United Kingdom · पूर्णवेळ
अर्ज करणारे पहिले व्हा
- अनुभव
- कोणतेही
- पगार
- —
- रिक्त जागा
- 1
- पोस्ट केले
- 22 तासपूर्वी
- कार्य मोड
- कार्यालयात
- शिक्षण
- Life sciences degree or equivalent
- सारांश
- अर्ज करणे आवश्यक आहे
तुम्ही जिथे काम कराल
नोकरीचे वर्णन
About the Role
Join IQVIA’s Site Management team as a Clinical Research Associate, contributing to multi-sponsor projects aimed at advancing healthcare outcomes. This position focuses on Oncology clinical studies and requires travel across sites within the United Kingdom.
Key Responsibilities
- Conduct various site monitoring visits including selection, initiation, on-going monitoring, and close-out in compliance with contract scope and Good Clinical Practice standards.
- Collaborate with clinical sites to develop, implement, and monitor patient recruitment strategies aligned with project objectives to improve study predictability.
- Provide protocol-related training to site teams and maintain consistent communication to address project expectations and resolve issues.
- Assess site adherence to protocol requirements and regulatory standards to ensure study quality and data integrity, escalating concerns when necessary.
- Track study progress by monitoring regulatory approvals, recruitment status, case report form completion, and data query management, supporting study start-up as needed.
- Ensure regulatory documentation is properly filed in the Trial Master File and that Investigator Site Files are maintained according to GCP and local regulations.
- Document monitoring outcomes thoroughly through visit reports, follow-up correspondence, and other required documentation.
- Work collaboratively with study teams to facilitate smooth project execution and address operational challenges.
Qualifications and Requirements
- Proven experience conducting independent on-site monitoring in the Oncology therapeutic area for unblinded clinical studies.
- Comprehensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Educational background in life sciences or equivalent professional experience.
- Availability and flexibility to travel to various clinical sites across the UK as required.
- Applicants should note that visa sponsorship is not available for this role.
Additional Information
IQVIA is a global leader delivering clinical research services and healthcare insights to foster medical innovation. The company upholds stringent ethical hiring practices and enforces zero tolerance toward candidate dishonesty. Compliance with truthful disclosure of qualifications and information throughout the recruitment process is mandatory.