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Systematic Review Methodologist - Jobs in Calgary, AB

Job LocationCalgary, AB
EducationNot Mentioned
SalaryNot Disclosed
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeFull Time

Job Description

POSITION LOCATION: Canada (home-based)POSITION TITLE: Systematic Review MethodologistPOSITION REPORTS TO: Sr. Manager, Medical WritingDEPARTMENT/UNIT NAME: Medical R&D - Research PM - Medical WritersJOB SUMMARY:As part of the Medical Writing team, the Systematic Review Methodologist independently conducts systematic literature reviews, meta-analyses, and network meta-analyses required for internal or external clients in the pharmaceutical, biotech, or academic clinical research sector. These reviews may be stand-alone projects or may lay the groundwork for a larger program of clinical research by exploring what is already known on a topic and summarizing that knowledge in a report and/or manuscript.AREAS OF RESPONSIBILITY:1. Consultation

  • Define research question(s) and frame questions for a review using the Population, Intervention, Comparison, Outcomes and StudyDesign (PICOS)framework.
  • Work with sponsors and investigators to develop the appropriate search strategy for the literature review given the research objectives (e.g., databases to search, languages and years of publications to be included, etc.).
  • Determine appropriate methods (e.g., meta-analysis, network meta-analysis) for analyzing the search results based on the aim of the review
2. Analyses
  • Conduct structured and/or systematic literature reviews, including screening of articles for eligibility based on pre-defined criteria and extract relevant data for use in the report, summary slide deck and/or manuscript.
  • Collaborate with colleagues as needed to conduct duplicate screening and data extraction and to resolve any discrepancies as described in the protocol.
  • Assess the quality of studies in the literature (e.g., internal validity, external validity, relevance, ethics approval, etc.) and establish a quality threshold (e.g., minimum sample size) with the goal of including studies that minimize bias.
  • Conduct meta-analyses and/or network meta-analyses if/as needed.
  • Synthesize and interpret data (e.g., direction and size of effect, homogeneity/heterogeneity of results, etc.).•Collaborate with a Statistician if/as needed for analysis and interpretation.
3. Writing
  • Develop systematic review protocols for sponsor approval and for use by the internal team to ensure clarity in aims and consistency in search strategy and decision-making processes.
  • Prepare reports, summary slide decks, and/or manuscripts for publication in accordance with reporting guidelines (e.g., PRISMA, MOOSE).
  • Contribute to grant proposals by identifying gaps in knowledge, helping to define the research question(s), and developing the overall approach to the literature review.
  • Edit and develop relevant SOPs, guidelines, and work instructions if/as needed.
4.Project Management
  • Independently manage timelines and deliverables.
  • Identify issues with the progress or design of the literature review and escalate issues that may significantly impact deliverables, timelines, or client relationships to line manager.
  • Provide project updates and meet with clients if/as needed; able to lead project kick-off meetings or roundtables.
  • Supervise other screeners and data extractors.
  • Contribute to the training and development of junior staff and fellows
QUALIFICATIONS:Job Experience & Education Requirements:
  • Post-graduate degree or undergraduate degree with professional certification(s) Level and 4-6 years related experience +substantial on-going job-related training
OR
  • Undergraduate university degree (Bachelor or Honors Bachelor) and 7-9 years related experience + continuous training and knowledge/skills upgrading
OTHER:
  • Degree in the health/life sciences field(e.g., biology, pharmacology, epidemiology)
  • Strong analytical and writing skills; Critical thinking and ability to interpret data is essential
  • Previous experience conducting systematic reviews, meta-analysis, and/or network meta-analysis
  • Training in GRADE methods and/or Cochrane methods
  • Experience in a clinical research environment and knowledge of the pharmaceutical industry
  • Ability to synthesize complex scientific information from the literature
  • Exemplary communication skills (verbal and written)
  • Demonstrated problem-solving, analytical reasoning, and decision-making skills
  • Ability to manage timelines and multiple projects
  • Experience in GI diseases an asset
WORKING CONDITIONS: Home-based
  • Accommodations for job applicants with disabilities are available upon request
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