Postdoctoral Research Fellow

1 week ago

Vancouver, British Columbia, Canada UBC Full time
Job Title

Postdoctoral Research Fellow - Drug Safety and Surveillance

Job Summary

The University of British Columbia (UBC) is seeking a highly motivated Postdoctoral Research Fellow to join the Hohl Research Group in the Department of Emergency Medicine. The successful candidate will conduct real-world drug safety and surveillance research using new adverse drug event data generated by a technological intervention designed to improve clinical communication of patients' adverse drug events.

Responsibilities
  • Lead the development of drug safety studies and a drug safety surveillance research program, including developing and selecting study protocols for a sentinel surveillance system and applying relevant pharmacoepidemiology theories, frameworks, processes, and measures.
  • Direct, supervise, and coordinate data collection, linkage, and analysis, including executing the research and surveillance plan.
  • Design mechanisms to quantify system- and provider-level factors associated with variation in ADE reporting.
  • Identify significant issues, barriers, or challenges that emerge in the post-marketing drug surveillance plan and develop mitigation strategies or resolutions.
  • Design studies in drug safety and effectiveness of treatments used to treat opioid poisoning and opioid use disorder using high-quality clinical datasets.
  • Maintain study documentation, including tracking and monitoring changes (adaptations) to the post-marketing drug surveillance strategies throughout the implementation process.
  • Complete data analysis to quantify and compare safety risks and effectiveness between drugs.
  • Participate in and provide research updates at regular meetings with other researchers and research assistants.
  • Review other study protocols as assigned, and discuss logistics with Research Investigators and the Research Program Manager. Ensure documentation is consistently maintained as directed by the study protocol.
  • Develop progress reports and updates for stakeholders and partners (as per the communication plan).
  • Develop briefing notes and presentations for stakeholders, including Public Health, government, and a health improvement network.
  • Complete other protocol-specific documentation as needed.
  • Act as a mentor and resource to Masters and PhD students.
  • Act as a resource to various research team members to identify real or potential problems and work to resolve these issues.
  • Contribute to and/or lead abstract, manuscript writing, presentations for submission to selected journals/conferences and grant proposals.
  • Other duties as required.
Qualifications
  • PhD in a relevant discipline required.
  • Relevant research experience in epidemiology; pharmacoepidemiology using qualitative or mixed methods; sociology and/or anthropology of medicine; health informatics; applied science, technology, and society perspectives.
  • Ability and experience in the area of pharmacoepidemiology and clinical research coordination.
  • Experience collecting and analyzing quantitative (mixed methods) data.
  • Ability to balance multiple commitments, short deadlines, and sensitive clinical or research issues.
  • Excellent communication skills, including strong writing, research, and interpersonal skills.
  • Innovative and creative thinking and a logical approach to problem-solving are also necessary.
  • Self-directed, self-motivated, and independent work skills.
  • Ability to work as part of a team.
  • Preference will be given to applicants with intermediate or advanced computer skills in the following software packages: MS Office (particularly Excel, Word, PowerPoint) and NVivo (qualitative data software package).
  • Experience with information technology in the health sector is considered an asset.
  • Familiarity with the field of drug safety, adverse drug event reporting, pharmacy practice, health technology implementations, health system research, or other potential research partners is an asset.
  • Familiarity and experience with grant-funded projects and study protocol requirements, including ethical conduct, ethics approval process, standard operating procedures, source documentation, and good clinical practice, is an asset.

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