Clinical Research Coordinator - Saskatoon, Canada - University of Saskatchewan

University of Saskatchewan

Verified Company

Saskatoon, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Clinical Research Coordinator:

Primary Purpose:

The Clinical Research Coordinator's primary purpose is to proficiently assist the Principal Investigator and associated research team through providing research coordination and support.

Success in the role will require some judgment and decision making, following procedures and guidelines set by the PI and collaborating with the research team.

Accountabilities

Acts as the primary contact and provides administrative and coordination support for research
Establishes and maintains strong working relationships with participants, researchers, and other study personnel; Liaises between study sponsors, staff, investigators and the CTSU
Ensures per protocol tasks are completed as per the schedule of assessments
Maintains organization and proper documentation of research materials
Ensures a safe environment for research participants and staff
Demonstrate a commitment to teamwork and positivity, along with an ability to create and nurture positive working relationships.

Duties
Study Set-up (20%)

Participates in site prequalification and qualification efforts
Ensures all required approvals are in place prior to enrollment
Assists in planning, implementation, and coordination of data collection
Recruits research participants and conducts eligibility assessment

Study Execution (50%)

Coordinates and conducts study visits and procedures per protocol
Obtains informed consent and conducts baseline testing
Maintains informed consent and oversees participant retention and compliance
Creates and maintains accurate patient source documents ensuring GCP
Participates in Health Canada inspections and sponsor audits
Prepares periodic and special reports, manuals, and correspondence

Study Close-out (5%)

Prepares and submits case report forms in compliance with SOPs and regulations

Research Administration 25%

Assists with monitoring and ordering of study specific supplies
Attends meetings including investigator, site initiation/close out, and monitoring visits
Provides general office duties, including distribution of memos and announcements, photocopying, mailing, and faxing

Qualifications

Education and Experience:

A Bachelor's Degree in a health-related field with 2 years of experience in clinical research or a Master's Degree in a health-related field.

Required Skills:

Proficiency with Microsoft Office (Word, Excel, Outlook)
Excellent verbal and written communication skills
Strong organizational, time, and project management skills
Experience conducting patientoriented research
Excellent interpersonal and ability to collaborate with team members
Detail oriented and able to exercise initiative and good judgement

Training:
The following certifications are required prior to commencing any study related procedures

TCPS2 Core Course
Safety Orientation for Employees (USask)
Off-Campus Activity Safety Plans (USask)
Canada GCP (CITI)
Clinical Research Coordinator (CITI)
Health Canada Division 5 (CITI)
Protocol Specific SOPs (N2)

Department:
Clinical Trial Support Unit

Status:
Casual

Employment Group:
Research Positions - Non-union

Full Time Equivalent (FTE): 0.5

Salary:
The salary range, based on 1.0 FTE, is $ per hour. The starting salary will be commensurate with education and experience.

Salary Phase/Band:
Salary Band 6

Posted Date: 2/10/2023

Closing Date: 3/9/2023

Number of Openings:1

Work Location:
On Campus

Criminal Record Check:
Not Applicable

Driver's License and Abstract Check:
Not Applicable

Education/Credential Verification:
Not Applicable

Vulnerable Sector Check:
Not Applicable

Please review the University of Saskatchewan's
health and safety requirements for faculty, staff and students in consideration of the COVID-19 pandemic.