Tasks, Duties & Responsibilities
• Provide a vital link between investigative site and sponsor team. This on-site position includes a variety of tasks with a support and practical base
• Within the nursing scope of practice, assists the Investigator with the care and evaluation of research participants.
• Utilizes nursing skills to coordinate research-related activities, and oversee all operational responsibilities of a clinical research study at the investigational site
• Responsible for ensuring subjects qualify for study prior to each dose and remains present for subject monitoring post-dose,
• Ensures randomization procedures are completed per protocol.
• Participates in the ongoing Informed Consent process with the Investigator to ensure that research participants and their families (if applicable) have their questions answered and understand the consent form, as well as participant's responsibilities in the study.
• Schedule patient visits, and contact regularly research patients to ensure that they are adhering to protocol-required medications
• Responsible for giving subject instructions at check-in and serves as the primary contact for subjects by being available to handle study-specific questions, concerns or events.
• Attends investigator's meetings, pre -study site visits, study initiation visits, and all other study-related visits by monitors or Sponsor representatives.
• Meet with monitors or clinical research associates (CRAs) during the conduct of periodic site monitoring visits and handling queries
• In collaboration with the Investigator and Project Manager, plans recruitment procedures for potential participants.
• Works closely with the Sponsor's team to ensure flow of study, and maintains communication with Sponsor or Sponsor Representative(s) throughout the clinical trial.
• With minimal supervision, and when necessary, accurately records and abstracts data from source documentation onto case report forms (paper or electronic CRF) in a timely manner. Maintains accurate and timely source documentation.
• Assures quality and completeness of source documents and case report forms collected during the course of the study.
• Performs quality checks on source documents specific to the study.
• After closeout visits has been conducted, prepares study documents for archiving according to timelines.
• Adheres to policies and procedures to ensure confidentiality, privacy and security of clinical research interactions and participant information, and responsible use of subject's research records in compliance with AGU Clinical Research policies.
The position offers competitive salary and benefits like housing and transportation allowances and health insurance.
Job Details
| Date Posted: | 2012-12-23 |
| Job Location: | Manama, Bahrain |
| Job Role: | Healthcare/Medical |
| Company Industry: | Education, Training, and Library |
Preferred Candidate
| Career Level: | Mid Career |
| Degree: | Certification / diploma |
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