Job Description

Reports to: Working under the direction of the Primary Investigator the CLINICAL RESEARCH COORDINATOR collaborates with the Medical Director (MD) and multidisciplinary health care team at in the following:

Recruitment of study participants (e.g. identifies and screens potential subjects, obtains informed consent, conducts and administers questionnaires or other data collection tools). Plans, implements and coordinates all aspects of data collection and source documentation, as per policy and ICH/GCP guidelines Identifies problems using assessment skills and reports any abnormalities to MD or health care team member Executes study: related administrative tasks such as collection of regulatory documents, ethics submissions, etc.; conducts telephone and/or clinical recruitment interviews to collect data using established criteria; coordinates patient visits schedule as per study protocol Executes all aspects of study visit (e.g. Data entry, assessment, EKG's, adverse events, monitoring safety, medication, questionnaires, sample collection, processing and shipment of samples according to clinical protocols) Co-ordinate the administration of Investigational Product to patients and orientates patients on study visits throughout the study protocol. Assesses study: related literature; and liaises with sponsor for monitoring/audits. Participates in Investigator meetings, Site Initiation Visit's, Study monitor visits and Study Close out visits. Involved in creation and modification of Standard Operating Protocols used for Clinical Trials Assist with Feasibility Questionnaires from study sponsors, responding and monitoring emails from study sponsors, patients, and various study team members
Additional duties

may include:

Obtaining vital signs; monitoring patients during injections/administering subcutaneous injections; specimen collection/handling; providing direct care to patients under the supervision of the physician; documenting procedures, operating and maintaining laboratory equipment; acting as liaison and networking with co investigators, sub investigators and sponsor companies.

Experience in a healthcare setting including clinical research is an asset including working knowledge of Word, Excel, Data entry, Phlebotomy, EKG, Urine analysis, and other basic laboratory skills.

Job Types: Part-time, Fixed term contract
Contract length: 12 months

Pay: $25.00 per hour

Benefits:

Flexible schedule On-site parking Store discount
Education:

AEC / DEP or Skilled Trade Certificate (preferred)
Experience:

Clinical laboratory: 1 year (preferred) Clinical Research: 1 year (preferred)
Work Location: Hybrid remote in Saskatoon, SK