Clinical Research Associate

Conducting and overseeing various aspects of the Blueprint group, including:

- Project management for the Blueprint research team
- Preparing any required Research Ethics Board submissions
- Preparing and maintaining budgets and/or timelines for funded and unfunded projects
- Developing study protocols, surveys, and interview guides
- Co-developing patient engagement strategies and coordinating engagement.
- Conducting interview and survey studies
- Designing and facilitating educational workshops and resources
- Assisting other group members with coordination of patient engagement
- Providing consultations on patient engagement
- Conducting qualitative and quantitative analyses
- Preparing presentations, reports, abstracts, and manuscripts for peer-reviewed scientific journals
- Co-developing accessible dissemination strategies.
- Participating and presenting at weekly research group meetings and teaching sessions

**Basic Requirements (Education/Experience)**:

- MSc in a health science related field or equivalent
- Minimum of 2 years of experience in a health research environment
- Evidence of training certification in Tri-Council Policy Statement -2 (TCPS-2) and the International Conference on Harmonization - Good Clinical Practice Guidelines (ICH-GCP)
- Evidence of training in Food and Drug Regulations, Division 5, and/or Device Regulations, as applicable
- Project management experience
- Previous experience managing research budget.
- Understanding of, and experience with, patient engagement in research
- Experience conducting interview, survey and/or focus group studies.
- Qualitative (e.g., thematic content analysis) and/or quantitative (e.g., analysis of survey results) research training and experience
- Demonstrated meeting and event organizing abilities.
- Strong time management skills and ability to effectively prioritize multiple projects.
- Flexible approach to meet demanding deadlines as required.
- Meticulous attention to detail to ensure data accuracy and adherence to protocol requirements.
- Computer literacy, including proficiency in NVIVO, Microsoft Word, Excel, and PowerPoint
- Excellent interpersonal skills to effectively collaborate with team members.
- Strong communication skills and demonstrated experience engaging with patients/caregivers and/or other diverse knowledge user groups
- Demonstrated ability to work collaboratively and effectively as both part of an interdisciplinary team and independently.

**Preferred Qualifications**:

- PhD in a health science-related field or equivalent
- Knowledge and experience in clinical epidemiology and biostatistics
- A working understanding of preclinical/basic science and its norms and language
- Knowledge of/experience with conduct of systematic reviews and meta-analyses and various meta-analytic software
- Previous research experience, publications
- Experience in a hospital research environment (translational, clinical or a combination)

**Contract Details**:
This is a full time, 1-year and 3-months contract to cover a maternity leave, with the possibility of contract renewal. Please note that this is an in-person (on site) position.

**Salary**: Min: $38.444/hr. - Max: $47.741/hr

**Comments to Applicant**:
**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._