Posted yesterday
Research Assistant I
@ Newfoundland and Labrador Health Services
Newfoundland and Labrador
SIGNALS
Overview
Newfoundland and Labrador Health Services is hiring a temporary full-time Research Assistant I in its Clinical Trials division until March 31, 2027, with possible extension. The role supports clinical trials from initiation to closeout, including patient data entry, study file maintenance, lab kit processing and patient testing at affiliated clinics. Hours are 75 bi-weekly on days, with pay at grade CG-24 of CAD 23.32 to 25.68 per hour.
Responsibilities:
- Enter confidential patient data into study databases
- Maintain study files per Health Canada guidelines
- Process lab kits, centrifuge blood and package shipments
- Travel to NLHS clinics to perform patient testing
- Support all phases of clinical trials
Requirements summary:
- Undergraduate coursework in health or social sciences
- One year of recent research experience with data entry and lab processing
- Proficiency in iMedidata Rave and Inform
- Proficiency in Microsoft Office
- Strong written and verbal communication
Tools & skills
Source and dates
Source type not verified · nlhs
- Employer posting date
- 2026-11-08
- First seen by our source
- 2026-11-09
- Source record updated
- 2026-11-09
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Allied health |
| Experience | 1+ years |
| Hours per week | 75 |
| Schedule | day |
| Travel | air: none · ground: moderate |
| Work setting | Hospital or clinic, Laboratory, Client sites |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English |
| Licences & certifications | Transportation of Dangerous Goods, Good Clinical Practice (GCP) with Health Canada |
| Education | Bachelor’s degree (required) |
| Fields of study | Health sciences, Social sciences |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Newfoundland and Labrador Health Services
| Field | Value |
|---|---|
| Headquarters | St. John's |
| Open jobs on Jobsy | 993 |
Job description
| Zone: Eastern Urban Zone Location: Health Sciences Centre Research Assistant I (Subject to Classification Review) Division of Research & Innovation - Clinical Trials Temporary Full-time (Until March 31, 2027, with possibility of extension) Management Support 29218TMP |
|---|
| Hours | 75 bi-weekly (8 hours; Days) |
| Salary | CG-24 (CAD23.32 - CAD25.68 per hour) |
| Competition Number | VAC0030646 |
| Posted Date | 2026-11-09 |
| Closing Date | 2026-11-16 |
| Demands, duties, qualifications | Job Summary Reporting to the Manager, Clinical Research, the Research Assistant I (RA I) will assist with confidentially obtaining patient information and entering it into the appropriate study database. The RA I will maintain study files by ensuring all documents are up to date and all correspondence is filed as required by Health Canada guidelines for clinical studies. The RA I will also assist with study questionnaires (mail or telephone, etc.), maintain an inventory of supplies and materials required for various studies (i.e. lab kits), while ensuring materials are not expired. The Research Assistant I will support and assist senior staff in preparing for study visits and regular study duties. This could include preparing study source documents for patient visits, labelling laboratory kits and stocking clinic rooms, travelling to NLHS clinics within the urban metro area to perform patient testing at affiliated NLHS clinics. Additionally, centrifuging patients' blood, pipetting the serum and packaging the bloods for shipment to the lab via FedEx as per transportation of dangerous goods guidelines, are all regular duties. The RA I will assist in all aspects of clinical trials from initiation to closeout, including but not limited to: patient screening, conducting assessments, randomization, data entry, documentation, and closeout preparation. The RA I will support the preparation and submission of invoices related to assigned clinical trials, ensuring accuracy and compliance with sponsor requirements. The RA I will coordinate and process patient reimbursements in accordance with study protocols and institutional policies. The RA I may also be required to support senior staff with environmental scans for various research topics as needed. Job Qualifications Education Undergraduate coursework in a health related or social sciences field is required. Current and continuing certification in Transportation of Dangerous Goods is an asset. Current and continuing certification in Good Clinical Practice (GCP) with Health Canada is an asset. Experience Minimum of one year of experience within the last three years working in a research setting including data entry and laboratory processing is required. Experience in report writing and conducting environmental scans are assets. Competencies (Knowledge, Skills & Abilities) Knowledge of research and evaluation approaches in various settings. Proficiency in Microsoft Office including Outlook, Word, Excel, and Powerpoint. Proficiency in iMedidata Rave and Inform. Demonstrated excellent written and verbal communication skills. Demonstrated individual leadership skills and autonomous critical thinking ability. Demonstrated time management skills as well as the ability to prioritize and work in a dynamic and collaborative environment. Demonstrated strong interpersonal skills and the ability to develop and maintain effective working relationships. Demonstrated strong team work skills and the ability to work collaboratively. Demonstrated effective research and analytical thinking skills. Ability to ensure confidentiality and work in an ethical manner. Other A satisfactory record of work performance and attendance is required. |
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