Job Summary
We are seeking an experienced Registered Clinical Research Nurse with a minimum of two years' relevant experience to join our dynamic research team. The successful candidate will play a vital role in coordinating and monitoring clinical trials, ensuring compliance with regulatory standards, and providing exceptional patient care throughout the research process. Immediate start availability is preferred, and the position offers an excellent opportunity to contribute to groundbreaking medical research within a supportive environment.
Duties
- Conduct patient assessments and monitor patient responses during clinical trials, ensuring safety and adherence to protocols
- Administer treatments, collect biological samples through phlebotomy, and manage data collection accurately
- Ensure compliance with FDA regulations, Good Clinical Practice (GCP), and other relevant guidelines
- Maintain detailed records of patient data in compliance with Good Clinical Practice (GCP) and FDA regulations.
- Collaborate with research teams to coordinate study activities, including scheduling appointments and managing study documentation.
- Ensure all clinical activities comply with regulatory standards, including FDA guidelines and institutional policies.
- Analyse clinical data using statistical software to support research findings and report outcomes effectively.
- Maintain meticulous documentation of trial procedures, patient records, and adverse event reports
- Analyse clinical data using specialised statistical software to support research objectives
- Supervise junior staff and coordinate with multidisciplinary teams to facilitate smooth trial operations
- Oversee data management processes, ensuring data integrity and confidentiality at all times
- Assist in preparing regulatory submissions and audit documentation as required
Qualifications
- Registered Nurse with current registration and valid practising certificate
- Minimum of two years’ experience in clinical research or a related healthcare environment
- Proficiency in medical terminology, data management systems, and statistical software applications
- Strong understanding of FDA regulations, GCP guidelines, and compliance management practices
- Demonstrated ability in patient monitoring, nursing procedures, and phlebotomy techniques
- Excellent analysis skills with attention to detail for accurate data collection and reporting
- Supervising experience is desirable but not essential; leadership qualities are advantageous
- Proven organisational skills with the ability to manage multiple tasks simultaneously in a fast-paced setting
This role offers a rewarding opportunity for qualified nurses passionate about advancing medical science through rigorous clinical research. The successful applicant will be integral to our mission of delivering innovative healthcare solutions while maintaining the highest standards of safety and compliance.
Pay: £25,000.00-£32,000.00 per year
Benefits:
- Company events
- Company pension
- Employee mentoring programme
- Employee stock purchase plan
- Flexitime
- Free parking
- On-site parking
- Referral programme
Ability to commute/relocate:
- Bedford, Bedfordshire: reliably commute or plan to relocate before starting work (required)
Application question(s):
- Do you live around Bedford, Milton Keynes, Northampton, or Luton?
Location:
- Bedford, Bedfordshire (preferred)
Work Location: In person
