Research Assistant at Queens University
Kingston, ON K7L 3N6, Canada -
Full Time


Start Date

Immediate

Expiry Date

23 Nov, 25

Salary

0.0

Posted On

23 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Word Processing, Research Design, Research, Medical Terminology, Professional Manner, Data Analysis, Clinical Trials, Grant Administration, Consideration, Time Management, Database, Clinical Research, Data Collection

Industry

Pharmaceuticals

Description

Research Assistant
About Queen’s University
Queen’s University is the Canadian research intensive university with a transformative student learning experience. Here the employment experience is as diverse as it is interesting. We have opportunities in multiple areas of globally recognized research, faculty administration, engineering & construction, athletics & recreation, power generation, corporate shared services, and many more.
We are committed to employment equity and diversity in the workplace and welcome applications from individuals from equity seeking groups such as women, racialized/visible minorities, Indigenous/Aboriginal peoples, persons with a disability, persons who identify in the LGBTQ+ community and others who reflect the diversity of Canadian society.
Come work with us!
Job Summary
The Research Assistant will participate in the coordination and administration of new and ongoing research projects within the Anesthesiology Research Group. This will include tasks such as: review of relevant published literature, preparation of written summaries of literature reviews; preparation of ethics and institutional approval applications with supervision; collection, storage and analysis of research data; participation in experimental design and optimization of Principal Investigator (PI) initiated research protocols; use of independent judgement to adapt procedures as the need arises; and communication and collaboration with various members of the interdisciplinary health care team within the Kingston Health Sciences and Queens University institutions. It may also include communication with external agencies and institutions regarding multi-centre project research.
Job Description

REQUIRED QUALIFICATIONS:

  • University degree in a relevant field. Master’s degree considered an asset.
  • Previous experience (minimum 3 to 5 years) working in a research environment, conducting research. Previous experience involving informed consents and data collection.
  • Knowledge of medical terminology is considered an asset.
  • Specialized training or experience in clinical trials and project management is considered an asset.
  • Understanding of research design, procedures, guidelines and standards governing clinical research is considered an asset.
  • Consideration may be given to an equivalent combination of education and experience.

SPECIAL SKILLS:

  • Respect diversity and promote inclusion in the workplace.
  • Interpersonal and communications skills (both verbal and written) to deal with a diverse variety of individuals in a professional manner and to provide clear and accurate information.
  • Ability to multitask, prioritize workload, and deal with multiple demands.
  • Skills in the preparation of informative and engaging presentations.
  • Time-management, and organizational skills as well as the capacity to take initiative, solve problems and suggest solutions.
  • Computer and office skills, including excellent knowledge of word processing, presentation, spreadsheet, and database applications.
  • Ability to work independently as needed.
  • Ability to exercise sound judgment with regard to the need for supervision and guidance.
  • Ability to work collaboratively with professionals in a team-oriented environment.
  • Familiarity with data analysis (qualitative and quantitative).
  • Interviewing skills for data collection.

SKILLS

  • Attention To Detail
  • Grant Administration
  • Research
Responsibilities
  • Participate in assessing, developing and executing strategies to support new initiatives for trials and other projects.
  • Participate in the development and implementation of research protocols under guidance. Conduct procedures, observe and record results. Make recommendations to adapt recruitment and data collection strategies as required. Participate as required in optimizing protocol implementation.
  • Collaborate on solutions to improve existing processes and participate in the implementation of solutions.
  • Communicate research results and current information in the field to internal and external stakeholders.
  • Liaise with other staff, labs, and outside agencies to gather information related to project activities, research promotion and meeting coordination.
  • Develop and maintain data logs.
  • Coordinate and use qualitative data collection strategies including internet searches, qualitative interviews with a range of stakeholders, document analysis and observation.
  • Review literature related to the project topics, prepare summaries of these reviews and collaborate with research teams to determine impact on research projects.
  • Collaborate with research teams and assist in the preparation of presentation materials. Present on behalf of project teams.
  • Provide regular updates at team meetings.
  • Assist with the development and preparation of resource materials (products of the research) and with materials for presentations.
  • Prepare summary project reports. Contribute to manuscripts.
  • Prepare, submit and renew REB applications with supervision.
  • Carry out project plans within allocated budgets.
  • Perform administrative duties including ordering supplies, and record keeping.
  • Other duties pertaining to smooth functioning of research unit.
  • Undertake other duties in support of the department/unit.
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