Bioluminux Clinical Research is an Integrated Research Organization (IRO) with investigator sites in the United States and the United Kingdom. Partnering with pharmaceutical companies, biotech firms, and CROs, the organization conducts high-quality clinical trials to advance medical innovation and improve healthcare outcomes. Bioluminux is dedicated to diversity in clinical research, ensuring equitable access to groundbreaking treatments through inclusive recruitment strategies. The company emphasizes scientific integrity, patient safety, and operational efficiency in every trial it conducts. Leveraging cutting-edge methodologies and strategic collaborations, Bioluminux is shaping the future of clinical research.
Role Description
This is an on-site contract (£13 - £15 per hour depending on experience), part-time role upto 3 days per week based in Milton Keynes for a Clinical Trial Study Coordinator. The role involves managing clinical trial operations, coordinating with investigators, and ensuring protocol compliance. Key responsibilities include patient communication, assisting informed consent processes, monitoring data collection accuracy, maintaining regulatory documentation, and ensuring adherence to clinical operating procedures. Additionally, the Coordinator will support recruitment, screen participants, and address protocol-related queries to ensure seamless trial execution.
Qualifications
- Experience with clinical trial processes, including facilitating patient understanding and obtaining documentation
- Experience in clinical settings and clinical skills like phlebotom
- Background in Clinical Research and Clinical Trials, with experience in trial management (preferred)
- Strong organizational, communication, and problem-solving skills
- Bachelor's degree in life sciences, healthcare, or a related field (preferred)
- Experience in clinical trial management systems (CTMS) will be an advantage
- Commitment to ethical research practices and participant safety