At a Glance
- Tasks: Coordinate and support clinical research studies while ensuring participant safety and data integrity.
- Company: Join a global leader in life sciences and clinical research.
- Benefits: Part-time hours, competitive pay, and opportunities for professional growth.
- Other info: Dynamic role with a focus on patient well-being and high standards.
- Why this job: Make a real difference in healthcare by contributing to groundbreaking research.
- Qualifications: Bachelor's degree in Nursing, NMC registration, and knowledge of clinical trials.
The predicted salary is between 29700 - 36300 £ per year.
Woodthorpe, York. Please note this is a part-time role, 8 hours per day, 24 hours per week (3 days per week).
We are looking for a Research Nurse for a global leader in life sciences analytics, technology and clinical research to support study sites in the coordination of Phase I-IV clinical research studies, ensuring that studies are carried out according to protocol, standard operating procedures, GCP, and other applicable guidelines and regulations.
RESPONSIBILITIES
- Coordinate clinical research studies conducted by a supervising principle investigator.
- Perform clinical set-up and preparation for the study, including labelling specimen collection tubes and containers, setting up equipment and documents.
- Responsible for the correct administration and custody of study drug according to site standard operating procedures.
- Perform a variety of complex clinical procedures on subjects including, but not limited to, ECG, sample collection including phlebotomy, spirometry, vital signs, cannulation, and cardiac telemetry monitoring.
- Collect, record, and report clinical data and findings appropriately in case report forms (CRFs).
- Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol.
- Update and maintain skills, training and knowledge of current best nursing practice and topics related to clinical research.
- Cooperate with study monitor and reserve sufficient time for questions during monitoring.
- Safeguard the well-being of the subjects and ensure and maintain high standards.
- Maintain a safe environment in accordance with Health and Safety Policies.
REQUIREMENTS
- Bachelor's degree or educational equivalent in Nursing and 1 year relevant experience; or equivalent.
- Registered Nurse with current NMC registration.
- Good knowledge of clinical trials.
- In-depth knowledge of the principles of Good Clinical Practices (GCP).
- Good skill at using MS Windows and Office applications.
- Effective written and verbal communication skills.
Research Nurse in York employer: hays-gcj-v4-pd-online
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