Administrative Assistant at University of Alberta

Ontario, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

01 Jan, 27

Salary

50000.0

Posted On

03 Oct, 26

Experience

22 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Industry

Hospitals & Health Systems

Description

This position has a term length of 1 year plus 1 day, with the possibility of extension.

Location - This role is in-person at North Campus Edmonton.

This position is responsible for assisting the Gastroenterology research group with core administrative tasks relating to all administrative aspects of conducting clinical trials in gastroenterology. Under the supervision of Dr Frank Hoentjen, the Administrative Assistant will provide day-to-day administrative support to the study team staff.

Specific responsibilities include regulatory & documentation administration, ongoing study maintenance, scheduling monitoring visits, study closeout and archiving, and administrative and operational support.

Responsibilities

Regulatory & Documentation Management

Maintain and organize regulatory binders and essential study documents.
Ensure all regulatory documentation is current, accurate, and audit-ready.
Track and ensure completion of required certifications (e.g., GCP, CPR, and annual CV updates for study staff).

Study Start-Up (Sponsor Package Focus)

Ensure all required site documentation is completed, collected, and returned to the sponsor/CRO in a timely manner.
Coordinate internal site readiness activities, including document collection and organization.
File and maintain all start-up documentation within regulatory binders.

Ongoing Study Maintenance

Maintain ongoing communication with sponsors/CROs on behalf of the site for document reconciliation.
Ensure regulatory documents remain up to date throughout the study.

Monitoring Visits & Communication

Schedule and coordinate monitoring visits, audits, and site visits.
Prepare and maintain documentation required for monitoring visits.
Organize and set up meetings (including virtual meetings via Microsoft Teams).
Act as a point of contact for sponsor document requests.

Study Closeout & Archiving

Assist with study closeout activities, including document reconciliation and completion of required checklists.
Ensure proper archiving of study files in accordance with institutional and regulatory requirements.

Administrative & Operational Support

Provide administrative and coordination support to the research team, including overflow supervisory tasks as needed.
Maintain internal tracking systems and logs to support study operations.
Assist with workflow coordination across multiple studies and priorities.

Qualifications

Minimum education: High School diploma
Minimum of 2 years working in an academic clinic research setting.
Experience working in an academic or research setting is preferred.
Experience in working with multi-disciplinary groups.
Proficiency in Microsoft Office and trial portals.
Problem solving, communication (oral and written), interpersonal, and organizational skills.
High level of accuracy and attention to detail required.
Commitment to providing timely and efficient service.
Knowledge of the research policies, procedures and guidelines for the major CROs and partners is preferred.
Demonstrated competencies in the areas of professionalism, results orientation, organizational
understanding, teamwork, flexibility and adaptability.

Application Instructions

Click "Apply Now" to submit your resume and cover letter.

Responsibilities

This position has a term length of 1 year plus 1 day, with the possibility of extension.

Location - This role is in-person at North Campus Edmonton.

Responsibilities

Regulatory & Documentation Management

Maintain and organize regulatory binders and essential study documents.
Ensure all regulatory documentation is current, accurate, and audit-ready.
Track and ensure completion of required certifications (e.g., GCP, CPR, and annual CV updates for study staff).

Study Start-Up (Sponsor Package Focus)

Ensure all required site documentation is completed, collected, and returned to the sponsor/CRO in a timely manner.
Coordinate internal site readiness activities, including document collection and organization.
File and maintain all start-up documentation within regulatory binders.

Ongoing Study Maintenance

Maintain ongoing communication with sponsors/CROs on behalf of the site for document reconciliation.
Ensure regulatory documents remain up to date throughout the study.

Monitoring Visits & Communication

Schedule and coordinate monitoring visits, audits, and site visits.
Prepare and maintain documentation required for monitoring visits.
Organize and set up meetings (including virtual meetings via Microsoft Teams).
Act as a point of contact for sponsor document requests.

Study Closeout & Archiving

Assist with study closeout activities, including document reconciliation and completion of required checklists.
Ensure proper archiving of study files in accordance with institutional and regulatory requirements.

Administrative & Operational Support

Provide administrative and coordination support to the research team, including overflow supervisory tasks as needed.
Maintain internal tracking systems and logs to support study operations.
Assist with workflow coordination across multiple studies and priorities.

Qualifications

Minimum education: High School diploma
Minimum of 2 years working in an academic clinic research setting.
Experience working in an academic or research setting is preferred.
Experience in working with multi-disciplinary groups.
Proficiency in Microsoft Office and trial portals.
Problem solving, communication (oral and written), interpersonal, and organizational skills.
High level of accuracy and attention to detail required.
Commitment to providing timely and efficient service.
Knowledge of the research policies, procedures and guidelines for the major CROs and partners is preferred.
Demonstrated competencies in the areas of professionalism, results orientation, organizational
understanding, teamwork, flexibility and adaptability.

Application Instructions

Click "Apply Now" to submit your resume and cover letter.