Nurse
mandatory * with DHA license or eligibility * Good communication skills * Computer proficient * Can join immediately Contract length: 24 months Job Types: Full-ti ...
The Department is conducting a research study titled A global multicenter, randomized, double blind, placebo controlled, adaptive designed phase III clinical trial.The primary aim of this study is to evaluate the efficacy, safety and immunogenicity of Recombinant Novel Coronavirus Vaccine in adults 18 years of age and older.
This is a short term project based position.
Responsibilities:
review research protocols, plan daily tasks and daily study flow of booked studies in conjunction with the Research Assistant, Laboratory technologist and study-specific coordinator
administer study vaccine to the subjects as per study protocol
perform routine technical procedures such as patients vital signs, IV cannulation, ECG, policies and procedures for approved research protocols
provide laboratory support services including phlebotomy and handling of required specimens (e.g. stool, urine, nasal swabs) using standard techniques; processing of specimens (centrifuging, processing, shipment handling and preparation)
provide emergency nursing care, crash cart management according to professional standards and in compliance with the policies and procedures of the Clinical Trials Unit
practice ICH-GCP as well as ensure compliance of ICH-GCP by Clinical Trails Unit staff
ensure compliance of established safety standards and maintain safe environment for patients, families, and clinical staff in accordance with regulatory and institutional health standards
coordinate study patient visit schedules with study research coordinators/clinical service coordinators
document and maintain accurate records (such as, patients assessment, subject specific specimens collected, specimen custody, specimen storage records, supply inventories, temperature logs etc.) as part of source documentation, regulatory, research and institutional requirements
ensure appropriate handling, disposal of biological and hazardous specimens/materials
inform the investigators and study coordinators of any adverse event, incidence and occurrence related to patient/visitor during their visit to the CTU, including a written report of the incident/event and the action(s)
Requirements:
Bachelors degree in Nursing (preferred) or Diploma in Nursing.
a valid PNC license
minimum of 2 years of work experience as a nurse in a hospital or related setting in inpatient and/or outpatient services
prior experience in working with research studies
good knowledge of use of computer and basic software
prior experience in operating basic medical equipment (eg. Infusion pump, ECG machine etc).
excellent interpersonal skills and communication skills
ability to handle diverse set of tasks for multiple studies
ability to work independently
strong communication skills, both verbal and written (English & Urdu).
Unfortunately, the job you are looking for is closed.
mandatory * with DHA license or eligibility * Good communication skills * Computer proficient * Can join immediately Contract length: 24 months Job Types: Full-ti ...
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