Clinical Research Assistant I
2 weeks ago
Assisting with the development of study protocols, surveys and interview guides
- Screening studies and extracting relevant data for systematic reviews
- Assisting with interview and survey studies
- Co-developing patient engagement strategies and coordinating engagement
- Designing and facilitating educational workshops and resources
- Assisting with relevant meta-analyses, as well as risk of bias assessments
- Assisting other group members with all stages of systematic reviews
- Assisting with manuscript writing
- Assisting with grant preparation and submissions
- Co-developing accessible dissemination strategies
**Basic Requirements**:
- Secondary diploma in a health science related field or equivalent
- Evidence of training certification in Tri-Council Policy Statement -2 (TCPS-2) and the International Conference on Harmonisation - Good Clinical Practice Guidelines (ICH-GCP)
- Evidence of training in Food and Drug Regulations, Division 5, and/or Device Regulations, as applicable
- Knowledge of basic statistics
- Meticulous attention to detail to ensure data accuracy and adherence to protocol requirements
- Strong communication skills and demonstrated experience engaging with patients/caregivers and/or other diverse knowledge user groups
- Computer literacy, including proficiency in Microsoft Word, Excel, and PowerPoint
- Excellent interpersonal skills to effectively collaborate with team members
- Demonstrated ability to work both independently and as part of an interdisciplinary team
**Preferred Qualification**:
- Experience conducting systematic reviews
- Bachelor's degree in a health science-related field or equivalent
- Quantitative (e.g. analysis of survey results) and/or qualitative (e.g. thematic content analysis) research training and experience
- Proficiency in meta-analyses and various meta-analytic software
- Experience conducting interview, survey and/or focus group studies
- Previous research experience, publications
- Experience in a hospital research environment (translational, clinical or a combination)
- Strong time management skills and ability to effectively prioritize multiple projects
- Flexible approach to meet demanding deadlines as required
**Contract Details**:
This is a full time, two-year contract with the possibility of renewal. Please note that this is an in-person (on site) position.
**Salary**: Min: $18.786/hr. - Max: $23.914/hr
**Contact Info**:
Name: Dr. Manoj Lalu
Title: Scientist
Program: Clinical Epidemiology
Ottawa Hospital Research Institute
Address: 501 Smyth Road, Ottawa
The Ottawa Hospital Research Institute is committed to building and sustaining a welcoming and supportive culture that promotes equity, diversity and inclusion for trainees, researchers, and staff. We are devoted to identifying and removing barriers that limit equitable access to opportunities within our organization. The Ottawa Hospital Research Institute strongly supports initiatives that encourage the participation of all groups, in particular the four groups defined in the Employment Equity Act (women, Indigenous peoples, persons with disabilities and members of visible minorities).
We thank all applicants for their interest. However, only those invited for an interview will be contacted. The Ottawa Hospital Research Institute is an equal-opportunity employer. Upon request, accommodations due to a disability are available throughout the selection process.
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