Policy, Planning and Research Analyst
NL Health Services - 1,010 Jobs
Newfoundland and Labrador
Closed
Job Details:
Location: Rotary Janeway Hostel
Policy, Planning and Research Analyst
Subject to Classification Review
Research & Innovation - Clinical Trials
Temporary Part-time (until December 31, 2026, with possibility of extension)
Management Support
19858TMP
Hours: 37.5 bi-weekly (8 hours; Days)
Salary: CG35 (CAD33.60 - CAD37.49 per hour)
Competition Number: VAC0017892
Posted Date: 2025-11-06
Closing Date: 2025-11-13
Job Summary
Reporting to the Manager of Clinical Trials, the Policy, Planning and Research Analyst will support the Clinical Trials Division Research Team in various aspects of procuring, preparing, conducting and reporting on clinical trials.
The Research Analyst will liaise with the Research Team for each trial; conduct reviews of relevant literature; prepare documents for submission to the Health Research Ethics Board (HREB) for trial/project approval and closure; maintain communication with the HREB throughout each trial; confer with the Program Director, Principal Investigator and sponsor representatives on project progress, compliance and interpretation; act as the principal liaison between the trial sponsor, investigator sites, monitors, data management, biostatistics, and other study personnel and service providers; participate in meetings with the Research Team and /or key stakeholders; assist in report composition; educate and update stakeholders on trial/project protocols; create databases, spreadsheets and enter/retrieve data; access clinical and routine databases; and maintain, store and retrieve study documentation.
Job Qualifications
Education
Completion of a Master's Degree in a health sciences or social sciences discipline (e.g. epidemiology, community/public health, biostatistics or health economics).
Experience
Experience in conducting clinical research including clinical trials.
Experience in Health Research Ethics Board submissions.
Competencies (Knowledge, Skills & Abilities)
Advanced knowledge of the current clinical trials regulatory environment, including Health Canada regulations, FDA Code of Federal Regulations, FDA Audit procedures and Tri-Council Policy.
Excellent knowledge of International Council for Harmonisation (ICH) - Good Clinical Practice.
Excellent organizational and administrative skills with attention to detail.
Demonstrated individual leadership skills and autonomous critical thinking ability.
Demonstrated time management skills as well as experience prioritizing and working in a dynamic environment.
Proficiency in Microsoft Office including Outlook, Word, Excel, and PowerPoint.
Demonstrated interpersonal, verbal, and written communication skills.
Effective research and analytical thinking skills.
Ensures confidentiality and works in an ethical manner.
Other
A satisfactory record of work performance is required.
Please submit your resume/cover letter, clearly demonstrating how you meet the required qualifications.
