Clinical Research Assistant

3 weeks ago


Greater Sudbury, Canada Health Sciences North Full time

**Clinical Research Assistant**:
**_CLINICAL RESEARCH ASSISTANT_**

***

Position Summary

Reporting to the Manager, Clinical Research Services, the Clinical Research Assistant will be responsible for assisting in various research tasks. The Research Assistant collaborates with Research Coordinators to provide support in organising multiple clinical research projects and ensuring that study protocols are implemented as required. This will include preparing and organizing research records, and ensuring that these are completed in compliance with Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) guidelines, and applicable regulations. The Research Assistant should possess strong communication and interpersonal skills, and work effectively in both a team environment and independently with mínimal supervision. This is a full-time, temporary (16 month), non-union, non-management position.

**Responsibilities**:

- Provides research operational support such as maintaining study documents, managing regulatory requirements, ethics submissions, departmental approvals, etc.
- Coordinates data management activities within clinical projects
- Acts as the primary communication point for research teams and the monitor / sponsor with regard to clinical data management
- Resolves issued queries in order to assure the accuracy of data
- Assist in monitoring visits and audits
- Assist with screening, recruiting, and obtaining informed consent from research participants
- Prepares required study documentation/updates and other required tools for the project
- Collaborates with medical staff to assure completeness and accuracy of documentation
- Contributes to general research activities (e.g., development of templates, policies, guidelines, and improved processes)
- Performs other related duties, as required and dependent on training and experience

**Qualifications**:
Education and Experience
- Undergraduate degree in a health, medical or biological sciences related field, or equivalent combination of education and experience, is required
- Minimum 1 year clinical research experience, is preferred
- Experience with Health Canada regulated drug/NHP/device trials is preferred

Special Skills / Training
- Training and experience with MS Office (Word, Excel, Outlook, PowerPoint etc.) required
- Demonstrated knowledge of and experience with research regulations and guidelines, such as the TCPS, ICH E6 (GCP), and Health Canada Food and Drug regulations preferred
- Post-graduate certificate in clinical research, or related topic preferred
- Certification in clinical research (e.g. SoCRA, ACRP) preferred
- Experience with processing biological samples is an asset
- Bilingual in English and French an asset

Other

Selection Process
- HSNRI reserves the right to conduct a formal interview process where required.

Hours
- Typically a 37.5 hour work week. Schedule may vary to meet demands, may be required to work outside of regular working days/hours.

Salary
- $24 to $26 / hr
- Commensurate with experience.

Application Deadline: Noon as of June 16, 2023

HSNRI is committed to providing accessible employment practices, in compliance with the Accessibility for Ontarians with Disabilities Act, 2005. Requests for accommodation can be made at any stage of the recruitment process, and applicants are asked to make their needs known.

Health Sciences North Research Institute (HSNRI) was established in 2011 as an independent not-for-profit corporation. Designed to bring together researchers, clinicians, regional partners and industry, HSNRI is the affiliated research institute of Health Sciences North (HSN).

We wish to thank all applicants, however, only those invited for an interview will be contacted directly.



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