Kelly Services Nurse Practitioner in Toronto, Canada
Kelly Scientific Resources (KSR) is a specialty service of Kelly Services, Inc., a leader in providing workforce solutions. Since its launch in 1995, KSR has provided staffing and placement services to a broad spectrum of industries, including biotechnology, chemical, consumer products, cosmetics, environmental, food sciences, medical/clinical, pharmaceutical, and petrochemical. Today, KSR leads the world in dedicated scientific and clinical research staffing. Visit www.kellyscientific.com to learn more and view a full listing of our opportunities.
Screening and offering clinical conduct, while providing treatment and care to all participants who meet study eligibility criteria and are enrolled in the clinical trial.
Responsible for monitoring the participants' safety through health status assessment and the performance of safety requirements. Responsible for the completion of assigned tasks within the department in accordance with study protocols, directives, SOP’s, GCP and applicable regulatory requirements.
Current practicing registration as a Nurse Practitioner with the College of Registered Nurses of Ontario and relevant, clinical experience in a community clinic setting, is preferred.
Current BCLS & First Aid certification, ACLS & GCP is an asset.
Experience performing PAP tests.
Previous CRO experience is preferable.
Ability to organize and maintain manual information sources, files and automated systems for storage and retrieval of data.
Provide support to protocol review meeting.
Excellent verbal, written and interpersonal skills are required.
Acute care experiences an asset. 12-Lead ECG interpretation.
Must be able to accommodate a flexible work schedule.
Taking medical history, physical examinations, and vital Sign/ECG interpretation on study subjects.
Performs PAP tests as needed
Determines eligibility of study participant.
Supervises study participants in clinical studies.
Reviews and signs medical laboratory results, ECGs, and adverse event reports related to studies.
Reports all Serious Adverse Events.
Administration of Investigational drug.
Attends study initiation visit meetings when requested.
Ensures informed consent is obtained and documented in accordance with GCP (Good Clinical Practice) prior to performance of any study-related procedures.
May perform Sub-Investigator responsibilities as assigned and delegated.
Ensures ongoing eligibility of study subjects.