Clinical Research Assistant - Toronto, Canada - FACET Dermatology

FACET Dermatology

Verified Company

Toronto, Canada

3 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

FACET Dermatology is looking for a Clinical Research Assistant to work closely with the clinical research coordinators to assist in study operations.

This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.

Responsibilities

Work collaboratively with research team members.
Maintenance of regulatory documents including the development and upkeep of study binders (electronic/paper).
Laboratory Processing
Assist with advance preparation for audits and site visits.
Check data for accuracy and completeness; score data; enter data, including data reentry; data cleaning
Provide support to other research team members, where necessary.
Assist with site training for site coordinators.
Develop other study documents as required.
Participate in studyrelated meetings
May involve conducting telephone and/or clinical recruitment interviews
Coordinating patient visits schedule as per study protocol;
Executing all aspects of study protocol involving patients visits

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Qualifications:_

Bachelor's degree, or recognized equivalent, in a health or sciencerelated discipline
At minimum 2 years clinical research and/or professional experience
Experience in management of research ethics (REB/HREBA) submissions
Knowledge of research regulations and guidelines preferred (such as ICH/GCP, Tri-Council Policy, Declaration of Helsinki, and Health Canada TPD (as required)
Excellent verbal and written communication skills in English
Intermediate to advanced skills in Microsoft Office, Outlook and basic computer skills
Excellent organizational and time management skills

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In order to be successful at this position, you should:_

Be a strong team member dedicated to exceptional service, efficiency, and safety.
Have experience with direct patient care
Have experience in conducting an informed consent discussion
Show proficiency in MS Office, Outlook and basic computer skills
Have experience with the use of electronic case report form (eCRF)
Be organized, flexible, and willing to step in where needed
Have attention to detail
Be selfmotivated and a fast learner

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Preferred requirements_

Bachelor's degree in a health or scientific related program
A thorough understanding of regulatory requirements
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
Experience with CRIO (Clinical Trial Management System) is a plus
Experience with administering vaccines is a plus

Salary:
From $50,000.00 per year

Benefits: