Guelph On Clinical trial assistant Jobs – 3 Openings This Week

Research Assistant (part-time)
Nutrasource —Guelph, ON
- $18–$22 an hour
- Part-time
- Microsoft Powerpoint
- Medication administration
- English
Quick apply
Budget Specialist, Clinical Research
Probity Medical Research Inc —Waterloo, ON
- $30 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Writing skills
- Finance
Quick apply
Budget & Contract Administrative Assistant
Probity Medical Research Inc —Waterloo, ON
- $25 an hour
- Full-time
- Microsoft Outlook
- Writing skills
- Finance
Quick apply

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Research Assistant (part-time)

Nutrasource -
Guelph, ON

Quick apply

Job details

Part-time
$18–$22 an hour

Qualifications

Microsoft Powerpoint
Medication administration
Clinical research
Process improvement
English
Recruiting
Standard operating procedures (SOPs)
Communication skills
Team coordination

Full job description

Job Overview:

The Research Assistant is responsible for research study activities such as assisting in study planning and set-up, assisting with study participant visits and study close out activities. They will be required to follow specific requirements of study protocols, regulatory requirements, policies, Standard Operating Procedures (SOPs) and Work Instructions (WI). The Research Assistant may assist with recruitment and coordinate study participant visits as directed by the study team. Part time / Casual

Primary Responsibilities:

Primary Responsibilities:

Assists the CRC in the coordination of assigned clinical research projects in accordance with Protocols, SOPs, WIs, and applicable regulations
Assists the CRCs and/or laboratory technicians on studies, including assisting in required start-up activities including but not limited to the following:
Preparing clinic source collection documents, time and events tables, and other required study materials
Planning and collaboration with vendors (safety laboratory, bioanalytic lab) for study set-up and clinic supplies inventory
Performs the following during the conduct of a clinical trial:
Assists in screening activities and provides support as required
Ensures set-up of clinic rooms, participant charts, and source document preparation prior to start of clinic visit activities
Assists in clinic activities including, but not limited to:
Assists in conducting clinic visits (admission, assist in dosing and randomization, discharge, and follow-up) as required
Follows-up and assists in ensuring volunteer eligibility prior to randomization
Witnesses investigational drug administration and other activities as delegated and required
In collaboration with the responsible teams, conducts all study-related activities according to protocol, SOPs, WIs, and applicable regulations
Checks for clinic updates, quality control findings, study monitor findings and addresses them with the guidance of the CRC
Escalates observations of concern to CRCs and Investigators as appropriate
Performs the following after the in-clinic phase of the clinical study and in preparation for site close-out:
Assists in close-out of study documentation, deviation reporting, CRF completion and sign-off, and other study-related reports/documentation
Assists in finalizing the study and/or subject logs
Assists with other close-out activities as required (return of study supplies, archiving, etc.)
Assists with monitoring participants’ compliance throughout the study
Assists in addressing day-to-day participant or study issues and escalates as appropriate
Assists with the preparation for regulatory inspections, sponsor or internal QA audits and monitoring visits, as required
Collaborates within and between teams during process improvement exercises, internal and external meetings, and other company-related initiatives and goals
Accommodates flexible schedules (available days, afternoons, nights, and weekends)

· Other duties as may be required and as training and experience allow

· Promotes GXP compliance across the organization

· Maintains an attitude and philosophy consistent with the company standards

Core Competencies:

Understands care of study participants, aspects of human subject protection and safety
Familiarity with Natural Health Product Regulations
Strong verbal and written communication skills in English (spoken and written)
Practices leadership and professionalism skills as well as understanding the importance of teamwork necessary for conducting a clinical trial
Takes pride in accomplished task and observes accountability and ownership
Proficient in MS Office, Excel, and Power Point

Education and Experience:

Pharmaceutical and/or clinical trial experience is an asset

· Certification and/or degree in a health, science or research related fields preferred

Job Type: Part-time

Pay: $18.00-$22.00 per hour

Work Location: In person

Quick apply

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Research Assistant (part-time)

Budget Specialist, Clinical Research

Budget & Contract Administrative Assistant

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