Clinical Research Coordinator

1 week ago

Guelph, Canada Nutrasource Full time

**Position Overview**

**Primary Responsibilities**:
Conduct the clinical research studies according to the study protocol, ICH GCPs, and SOPs.

Be knowledgeable of the protocol so that all study activities are completed correctly.

Obtain written informed consent from each study participant prior to participation in the study.

Screen the potential study participants according to the protocol’s inclusion and exclusion criteria.

Schedule study participant visits as per protocol.

Perform delegated protocol specific activities completely and accurately.

Obtain vital signs as required per protocol (i.e. blood pressure, temperature, heartrate, respiratory rate, weight & height).

Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol.

Obtain all necessary documentationas required by the protocol.

Monitor and report all adverse experiences and abnormal results to the Investigator, CRO and IRB if necessary.

Create & complete source documents and any other research documents required for the successful conduct of a clinical research study.

Ensure ISF is kept current for trial.

Liaises with the Principal Investigator and Site Director during course of trial.

Enter data into EDC and query resolution.

Maintains an attitude and philosophy consistent with the Company's standards.

**Core Competencies**:
Knowledge of medical terminology

Knowledge of general research procedures and regulatory requirements

Strong communication and interpersonal skills

Detail oriented with exceptional organizational skills

Ability to work in a team

Proficiencywith MS Office suite

**Qualifications**:
Bachelor of Science degree or post-grad diploma

Minimum 1-2 years of clinical research training or experience

GCP certification desirable

CCRA / CCRP / ACRP certification preferred

Previous experience with phlebotomy and intravenous catheters is an asset

**Must be available weekday and early mornings**

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

**Job Types**: Part-time, Fixed term contract, Casual

Schedule:

- 10 hour shift
- 12 hour shift
- 8 hour shift

Work Location: In person

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