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- Acts as the lead and subject matter expert in conducting clinical studies according to FDA/GCP and ICH regulations and guidelines.
- Provides medical care to patients, always ensuring patient safety comes first.
- Schedules subject visits within protocol windows, ensuring scheduling capacity is improved.
- Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, blood samples, etc.).
- Performs clinical assessments of participants, monitors laboratory safety reports, and communicates any serious or potentially serious adverse events as per the company procedure.
- Serves as a primary point of sponsor contact for all research activities for studies assigned.
- Acts as a back-up to direct people manager. This includes but is not limited to, coordinating and assigning work to team members, scheduling, and monitoring time.
- Involved in the interview and hiring process of new team members.
- Assists in the training of new team members and provides mentoring.
- Provides input into evaluations performance reviews of team members.
- Performs other study related duties as qualified by documented training.
- A qualified Nurse, a registration with no limitations to practice within the Nursing and Midwifery Council (Adult)
- Extensive nursing experience
- Clinical Research experience (Preferred)
Director of Nursing - Hexham, Northumberland, United Kingdom - OH Sourcing
OH Sourcing
Hexham, Northumberland, United Kingdom
1 month ago
Description
Lead Clinical Research Nurse opportunity to join leading Contract Research Organisation at their site in Hexham.The Position:
Full time, 37 hours, Permanent
Monday to Thursday 8am-4:30pm, Friday 8am-4pm
As a Lead Clinical Research Nurse, you will be a key member impacting the development and research for therapeutics for patients.
The Requirements: