Research Assistant II

at  LunenfeldTanenbaum Research Institute

Toronto, ON, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate01 Oct, 2024Not Specified22 Sep, 20242 year(s) or aboveData Collection,Computerized Systems,High Pressure Situations,Time Management,Communication Skills,Organization Skills,Databases,DiplomacyNoNo
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Description:

Reference Number: 000002004
Posted Date: 9/11/2024
Closing Date: 10/1/2024
Department: LTRI (Paediatrics)
Position: Research Assistant II

ORGANIZATION DESCRIPTION:

Department of Paediatrics, Mount Sinai Hospital, a University of Toronto affiliate, is one of the world’s leading centers in neonatal perinatal intensive care. With ground-breaking discoveries in research areas in Women’s and Infants’ Health, the Department of Paediatrics is committed to excellence in clinical care, health research and the training of young investigators. Strong partnerships with other 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:

We are seeking a highly organized, detail-oriented, and dedicated temporary part time (12 month contract) Research Assistant to join the Sepsis Program, which includes both research and quality improvement work. The Research Study Assistant will work independently under the supervision of the Principal Investigator.

SUMMARY OF JOB FUNCTIONS (WILL INCLUDE BUT ARE NOT LIMITED TO):

  • Medical chart review and data abstraction
  • Assisting with the collection, management and analysis of qualitative and quantitative data
  • Assisting with database creation and maintenance
  • Assist supervising Principal Investigator in preparing reports of study progress
  • Assisting with preparation of written materials: research ethics board applications and reports, consent forms, manuscripts, research reports, poster and presentation submissions.
  • Engagement with the lead investigators, research team, and clinical providers throughout the research process.
  • Usually works from/with standard procedures and practices and will assist in improving new ones or in modifying existing methods, practices and procedures.
  • Responsible for maintaining study documents and other research files
  • Assist with preparation and facilitations of submissions to the Research Ethics Board which includes applications for new studies, renewals, staff additions
  • Participating in data collection for quality improvement audits
  • Liaise with the NICU Quality Improvement Team to coordinate meetings and execute actionable items

MINIMUM REQUIREMENTS

  • Bachelor’s degree in a health-related field
  • Minimum 2 years of experience in an academic or clinical/ research setting

QUALIFICATIONS

  • Familiarity with research processes including data collection and data entry
  • Ability to work independently in a dynamic environment with interdisciplinary research teams
  • Excellent coordination, time management, and organization skills and flexibility to adapt to changing workload
  • Ability to manage confidential and sensitive data and information; maintaining professionalism, diplomacy, and tact in high pressure situations
  • Strong interpersonal, verbal, and written communication skills
  • Exceptional attention to details and proven ability to learn new skills
  • Skilled in the use of computerized systems, equipment and databases

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

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Clinical Pharmacy

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A health-related field

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1

Toronto, ON, Canada