Nurse - Clinical Trials

Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are currently looking for a Nurse to join our clinic location in Scarborough.

The function of the Study Nurse I is to ensure all investigational products are handled according to GCP guidelines and the Standard Operating Procedures (SOPs) of Pharma Medica Research Inc. (PMRI) . Monitor the health and safety of volunteers throughout the conduct of clinical studies. The Study Nurse I reports to the Manager, Clinical Operations and / or designate.

Responsibilities

• Work or assist in handling investigational product related activities, including but not limited to accountability, repackaging, dispensing, receipts, archiving, disposal at PMRI under the supervision of the investigator / institution.
• Maintain records of investigational product delivery to PMRI, inventory, the use by the subject, and the return to the sponsor, the disposal, or archiving of unused product.
• Explain the correct use of the investigational product / other medications to the subjects and ensure that the subjects follow the instructions properly.
• Administer investigational products for the conduct of a clinical study using different dosing methods in accordance with protocol requirements.
• Administer any concomitant / additional medication under the supervision / order of the Investigator.
• Ensure the health and safety of the subjects by performing various types of health assessments (e.g. medical history, vital signs,      electrocardiograms, telemetry, health monitoring, and safety follow up etc.).
• Communicate and take care of the volunteers / subjects' health or other study related concerns.
• Perform other study procedures (e.g. conduct various consents with volunteers, collect / process samples, record adverse events, and assist      investigators etc.).
• Maintain and document emergency drugs, products, and supplies in the clinic, including crash cart, emergency medication, AED, etc.
• Assist in editing and reviewing Standard Operating Procedures (SOPs).
• Ensure all duties are conducted in compliance with SOP, regulatory guidelines and applicable regulations.
• Oversee on-floor clinical activities together with the Group Leaders / Study Coordinators to ensure study procedures comply with protocol and    SOPs.
• Perform screening procedures such as but not limited to : blood sample collection, sample processing and storage, vital signs, ECGs, etc.,    according to the study protocol and / or SOP requirements, as required.
• Assist in conducting hands-on training to other clinic employees as required.
• Other duties as required.

Qualifications :

We Offer

Please note all applications must be eligible to work within Canada.

PMR I is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.

We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.

If you meet the qualifications and are looking for an exciting place to work, apply today!