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Health Research jobs in Victoria, BC

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    • Manage the planning, execution, progress and completion of assigned clinical research projects.
    • As the primary sponsor liaison and advocate, the Clinical…
    • View all Alimentiv jobs - Victoria jobs - Clinical Project Manager jobs in Victoria, BC
    • Salary Search: Imaging Clinical Project Manager (1 -Year Limited Term) salaries
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    • Location: Victoria, Courtenay, or Nanaimo, BC.
    • (Hybrid service delivery model: virtual and in-person).
    • We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
    • Conducts market research including customers and competitors activities.
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    • Conducts or reviews a variety of research produced by research and policy organizations, universities, governments,.
    • Maintain expertise in safety and health.
    • Keeps current on literature and research in the field; and provides up-to-date best practice information.
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    • Keeps informed on current literature and research.
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    • Proactively identify key business opportunities, research and recommend enhancements / modifications, develop strategies to achieve recommendations and work…
    • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries…
    • Participate in the promotion of Alimentiv as a global research organization, by contributing to the development, publishing, and reporting of project data.
    • Experience working in a national charitable or health-related organization.
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Job Post Details

Imaging Clinical Project Manager (1 -Year Limited Term) - job post

Alimentiv
2.5 out of 5 stars
Victoria, BC•Remote
$89,000–$148,000 a year - Full-time

Job details

Pay

  • $89,000–$148,000 a year

Job type

  • Full-time

Full job description

As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute, manage and monitor regional, single modality or therapeutic area clinical research projects. Utilizing existing templates, processes and programs as a guide, he or she will adapt/develop, implement, monitor and be accountable for project protocols, operational plans, risk management, resources, project tools/materials, documents and timelines. The successful candidate will be managing the day to day activities and performance of a multidisciplinary project team, ensuring all decisions align with corporate, industry, sponsor and regulatory requirements.

Project Management

  • Manage the planning, execution, progress and completion of assigned clinical research projects.
  • Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.
  • Maintain operational, financial and regulatory integrity and safety.
  • Develop and/or participate in the development of project communications, training, regulatory submissions and/or audits and selection of third party vendors as required.

Documents and Tools

  • Manage a cross-functional team to ensure the appropriate creation, delivery, maintenance and disposal of all related data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case report forms and instructions.
  • Prepare investigator updates and other project related reports as required to support the proper conduct and execution throughout the life cycle of assigned projects.

Project Team Performance

  • Identify, assign and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis and/or final report writing and publications.
  • Ensure task completion performance meets or exceeds quality standards and sponsor/client, project and regulatory expectations and guidelines.

Client/Sponsor Support

  • Act as primary liaison throughout the project life cycle ensuring client/sponsor expectations are appropriately managed by addressing and resolving queries/issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/client with project status and update reports.

Qualifications

  • Applicants should have a minimum of one to three years of related work experience with ongoing training, and a three-year College Advance Diploma/Degree in a relevant field of study, preferable in (Health) Sciences or Clinical Research.
  • Experience within Imaging is an asset
  • The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results.
  • Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results.
  • Ability to engage in continuous learning and self-development.
  • Ability to continually foster teamwork.

Working Conditions

  • Home Based
  • Occasional travel
    • Accommodations for job applicants with disabilities are available upon request
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