Research Associate

2 weeks ago

Toronto, Canada Lunenfeld-Tanenbaum Research Institute Full time

**Reference Number**:000001892
**Posted Date**:11/13/2023
**Closing Date**:11/24/2023

**Department**:LTRI (Healthy Ageing and Geriatrics Program)
**Position**:Research Associate

**POSITION TITLE**
- Research Associate**DEPARTMENT**
- LTRI (Healthy Ageing and Geriatrics Program)**EMPLOYMENT TYPE**
- Temporary, Part-Time**HOURS OF WORK**
- 7.5 to 24 hours per week (targeting 10 hours per week)**EMPLOYEE GROUP**
- Non-Union**REPORTS TO**
- Principal InvestigatorThe Lunenfeld-Tanenbaum Research Institute of Mount Sinai Hospital, a University of Toronto affiliated research centre, is one of the world's leading centres in biomedical research. With ground-breaking discoveries in research areas such as diabetes, genetic disorders, cancer and women’s and infants’ health, the Institute is committed to excellence in health research and the training of young investigators. Strong partnerships with the clinical programs of Mount Sinai Hospital ensure that scientific knowledge is used to promote human health. Your significant contributions will assist in maintaining our momentum in advancing our research.

**Position Overview**:
This exciting administrative position will allow you to become an integral part of the busy, dynamic, and growing high profile Health Ageing and Geriatrics Program at Sinai Health and the University Health Network (UHN). To support us on our journey, Sinai Health is looking for an research professional to provide research support and the support of strategic clinical initiatives of its Healthy Ageing and Geriatrics Program.

In your role, you will be expected to exercise sound judgment and independence in supporting Dr. Richard Norman and other program staff while managing the day-to-day administrative activities related to the delivery of the Surgical Ace initiative.

**Responsibilities**:

- Collaborate with the Principal Investigator, Dr. Richard Norman, to ensure the successful execution of the Surgical Ace study.
- Manage and organize all clinical research data, including patient records, lab results, and case report forms.
- Conduct in-depth data analysis, utilizing statistical software and relevant tools, to extract meaningful insights and trends from the collected data.
- Ensure data integrity and accuracy through meticulous data validation and quality control procedures.
- Regularly perform audits of clinical data to ensure compliance with study protocols, regulatory guidelines, and Good Clinical Practice (GCP) standards.
- Maintain a comprehensive and up-to-date database of study participants and their clinical histories.
- Collaborate with the study team to develop and update study protocols, standard operating procedures, and case report forms.
- Assist in the recruitment and screening of eligible participants for the Surgical Ace study.
- Collect and manage informed consent documentation from study participants.
- Coordinate patient visits, clinical assessments, and data collection procedures as outlined in the study protocol.
- Develop and maintain a system for tracking and reporting adverse events and serious adverse events in accordance with regulatory requirements.
- Prepare, organize, and maintain study documentation, including regulatory submissions and ethics committee approvals.
- Collaborate with the research team to ensure proper participant enrollment, and follow-up, according to the study timeline.
- Support the writing and preparation of manuscripts, abstracts, and presentations for scientific conferences and publications.
- Contribute to the interpretation of clinical data and assist in the generation of meaningful findings.
- Assist in preparing and delivering presentations of research findings to internal and external stakeholders.
- Participate in meetings, including study team meetings, investigator meetings, and external audits.
- Ensure compliance with all regulatory requirements and guidelines, including local ethics committee regulations.
- Keep abreast of developments in clinical research, surgical procedures, and relevant therapeutic areas.
- Provide training and mentorship to junior staff or research assistants when necessary.
- Ensure the security and confidentiality of clinical research data.
- Perform any other duties and responsibilities related to the Surgical Ace study as directed by Dr. Richard Norman and the study leadership.

**Job Requirements**:

- Requires the successful minimum completion of a Medical degree, PhD, or recognized equivalent, in a health or science-related discipline with 3+ years clinical and/or professional experience including at least 1 year clinical research-related experience or equivalent combination of education and experience
- Well-developed organizational and time management skills
- In-depth knowledge of Good Clinical Practice
- Experience or familiarity in Quality Assurance practices
- Ability to follow established trial protocols, guidelines, procedures, and standards
- Ability to effectively manage multiple proj

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