Clinical Research Coordinator - Oncology Trials
- glasgow, scotland, G1 1AA, United Kingdom
- Permanent·Hybrid
- Full time
- £45,000 - £45,000 Per Annum
Job Description
About the Role
Our client is looking for a meticulous Clinical Research Coordinator to support their vital Oncology Trials . This hybrid role allows for a balance of remote administrative tasks and essential on-site patient interaction and data management in Glasgow . You will be crucial in ensuring the smooth execution of clinical studies, from patient recruitment and data collection to regulatory compliance. This position is ideal for an organized and dedicated individual passionate about advancing cancer treatments through rigorous clinical research, working within a supportive team environment that values patient well-being and scientific integrity.
Key Responsibilities
- Coordinate all aspects of clinical trials, including patient recruitment, screening, and scheduling.
- Collect, manage, and ensure the accuracy of clinical trial data, adhering to Good Clinical Practice (GCP) guidelines.
- Educate patients and their families about trial protocols and procedures.
- Liaise with investigators, research staff, sponsors, and regulatory agencies.
- Maintain trial documentation, source records, and regulatory files.
- Assist with study monitoring visits and regulatory audits.
Requirements
- Bachelor's degree in a relevant scientific or healthcare field.
- Minimum of 2 years of experience as a Clinical Research Coordinator or similar role.
- Strong understanding of clinical trial processes and regulatory requirements (e.g., GCP, FDA regulations).
- Excellent organizational, communication, and interpersonal skills.
- Proficiency in using electronic data capture (EDC) systems and other clinical trial software.
- Ability to manage multiple tasks effectively in a hybrid work setting, requiring both remote work and on-site presence in Glasgow .
Benefits
- Competitive salary and benefits package.
- Hybrid work arrangement offering flexibility.
- Opportunity to contribute to life-saving cancer research.
- Continuous professional development and training opportunities.
- Supportive team environment focused on collaboration.
- Paid time off and pension contributions.


