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Research Associate, Ccfv Jobs
Company | IWK Health |
Address | Halifax, Nova Scotia, Canada |
Employment type | TEMPORARY |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-07-16 |
Posted at | 10 months ago |
Click here to apply as an internal applicant.
- Work with project team, community partners, external partners, vendors, and others to ensure all project deliverables are completed and milestones are met
- Assist and support the Project Manager with administrative related issues when required
- Provide overall coordination of research studies in accordance with Standard Operating Procedures, Good Clinical Practice, and funder guidelines under the oversight of the investigator
- Develop study-related documents, which may include protocols, ethics correspondence, interview guides, consent forms
- Communicate with participants and facilitate study recruitment
- Facilitate the planning, organization and administration of research studies, under the direction of the assigned Project Manager and Principal Investigator
- Conduct or support collection (surveys, interviews, focus groups, etc.) and analysis (qualitative coding, NVivo analysis, statistical, etc.) of qualitative and/or quantitative study data
- Develop and maintain methods of tracking information through databases and spreadsheets
- Organize, communicate, and evaluate team objectives and progress of project
- Conduct scientific literature searches including abstracting data from published sources, summarizing articles and maintaining a bibliographical database
- Write, edit, and disseminate research reports, academic papers and research presentations in cooperation with the research team
- Assist with grant application preparation and writing
- File and manage study documents (interview/focus group guides, etc.), participant documents (consent forms, etc.), data files (data entry, audio recordings, transcripts, etc.), and other study-related materials
- Competency in other language is an asset
- Experience with academic writing and project-based reports
- An understanding of the principles of Equity, Diversity, Inclusion, Accessibility and Reconciliation (EDIAR) and how they relate to research practice
- Completion of a research methods course or equivalent experience with qualitative, quantitative, and/or mixed-methods research
- An understanding of a research environment and guidelines/standards that inform different areas of research practice (e.g. Good Clinical Practice (GCP) and principles of Ownership, Control, Access and Possession (OCAP))
- Well-developed organizational, time management and daily planning skills including creating work schedules, monitoring progress toward goals, tracking details, data, information, and activities
- Able to work cooperatively and effectively with others to set goals, resolve problems and make decisions that enhance Center effectiveness
- Able to work well independently as well as within a multi-disciplinary team environment and able to initiate own work schedule without regular supervision while working off-site
- Experience conducting community-based research considered an asset
- Able to produce high-quality written work (e.g., correspondence, study documents, reports, summaries, tables, charts, graphs, manuscripts, etc.)
- Excellent communication and interpersonal skills; able to speak, listen, and write in a clear, thorough and timely manner using appropriate and effective communication tools and techniques with a variety of audiences
- Undergraduate degree in social sciences/health services or related field; Master’s degree preferred
- Highly organized and able to multi-task when required
- Proven ability to publish in peer-reviewed journals and/or produce other research outputs aimed at a variety of stakeholder or knowledge-user audiences
- Able to establish and maintain positive working relationships with others, both internally and externally
- Experience with REB submissions considered an asset
- Demonstrate a high level of time management and decision-making skills when setting priorities based on project deadlines and milestones
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- Proficiency in using qualitative (e.g., NVivo, etc.) and quantitative analytic software (e.g., SAS, etc.) an asset
- May be required to work a combination of on-site at CCfV and from home
- Relevant experience within a university, hospital, or comparable environment in a research setting
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