Clinical Research Coordinator- 1-year Contract

4 weeks ago

Hamilton, Canada The Wharton Medical Clinic Clinical Trials Inc Full time

Clinical Research Coordinator Maternity leave

The Wharton Medical Clinic Clinical Trials Inc - Hamilton, ON

Overview

The job is part time (3-4 days/week) 1 Year contract

**CLINICAL RESEARCH COORDINATOR (3-4 days/week)**

**QUALIFICATIONS**
- Bachelor's degree, or recognized equivalent
- Strong knowledge of medical terminology
- Holds recognized certification in clinical research (ACRP or SOCRA)
- Minimum two (2) years clinical research experience preferred
- Autonomous clinical critical thinking ability
- Training in ICH/GCP
- Knowledge of IATA shipping regulations and basic laboratory procedures
- Excellent organizational and time management skills required
- Strong analytical and problem solving skills
- Excellent interpersonal, verbal and written communication skills required
- Ability to set priorities and work independently with accuracy in a dynamic environment
- Proficiency with MS Office software - Word and Excel desired
- Ability to perform venipuncture is an asset

**RESPONSIBILITIES WILL INCLUDE, BUT ARE NOT LIMITED TO**:

- Conduct the clinical research study according to the study protocol, GCP, and SOPs
- Understand, manage, and comply with multiple study protocols ensuring all study activities are completed correctly
- Identify and recruit potential patients for participation in clinical research studies according to research ethics board recommendations
- Administer and document informed consent from each study participant prior to participation in the study
- To screen the potential study participants according to the protocol’s inclusion and exclusion criteria
- To schedule study participant visits as per protocol
- To perform delegated protocol specific activities completely and accurately
- To obtain vital signs as required per protocol (i.e. blood pressure, temperature, heart rate, waist measurement, weight & height)
- To perform blood & urine collection, processing and shipping, as well as other on-site patient testing as needed (e.g. ECG, pulmonary function testing)
- Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol
- To obtain all necessary documentation as required by the protocol (i.e. ECG, echocardiogram or pulmonary function test results)
- To monitor and report all adverse experiences and abnormal results to the Investigator, Sponsor and IRB if necessary
- To create & complete source documents and any other research documents required for the successful conduct of a clinical research study
- Perform data entry into eCRF within required timelines after each study visit and respond to data queries
- Meet with the Sponsor's representatives to discuss the conduct of the study and review study data
- Participate in inspections by regulatory authorities or audits by sponsors.
- Sanitize and clean equipment and room after patient visit according to Public Health Guidelines

**Job Types**: Part-time, Contract

**Job Type**: Part-time

**Salary**: $20.00-$22.00 per hour

**Benefits**:

- On-site parking
- Paid time off

COVID-19 considerations:
All staff and visitors including patients wear masks and complete prescreening COVID-19 questionnaires.

**Experience**:

- Clinical Research: 1 year (preferred)
- venepuncture/phelobotomy: 1 year (preferred)

Work Location: One location

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