Jobs · Information Technology

Sr Clinical Research Associate - Oncology

UBC · United States · 6 days ago
RemoteRemoteInformation TechnologyFull-time

Brief Description

Maintains compliance with protocols and ensures accurate data collection.

Specific Job Duties

  • Performs remote and on-site monitoring in accordance with project timelines.
  • Schedules travel in accordance with project and UBC policies.
  • Submits expense reports within UBC requirements.
  • Attends project team meetings, department meetings, and one-on-one meetings with the manager.
  • Completes site monitoring reports and letters according to UBC and/or sponsor standards.
  • Follows up on site issues and action items according to UBC and/or sponsor timelines.
  • Enters site visit dates, monitoring report dates, follow-up letter sent dates, and site contacts into UBC's CTMS.
  • Maintains regular contact with assigned sites according to study requirements.
  • Completes SOP reviews, training assessments, and documentation within requested timelines.
  • Mentors and trains junior level CRAs.
  • Aids in preparing and delivering presentations for UBC CRA training, departmental training, and/or sponsor-specific training.
  • Assists with additional tasks as needed, which may align with other departments at UBC.
  • Completes site management and monitoring activities in accordance with project plans and timelines.
  • Assists with other duties as assigned, which may align with other departments at UBC.

Supervisory Responsibility

None

Desired Skills And Qualifications

  • Bachelor’s degree in Life Science preferred or equivalent years of industry and clinical research experience.
  • Minimum of 36 months on-site monitoring experience, including site selection, initiation, management, and monitoring activities.
  • Comprehensive knowledge of medical terminology and regulatory guidelines.
  • Excellent critical thinking and resolution skills.
  • Excellent written and verbal communication skills in English and local language (as applicable).
  • Experience working in clinical trials and observational studies preferred.
  • Experience and familiarity with CTMS, eTMF, EDC, and Microsoft Office applications.
  • Proven ability to deliver highly accurate work and adhere to deadlines in a fast-paced environment.

Benefits

  • Remote opportunities
  • Competitive salaries
  • Growth opportunities for promotion
  • 401K with company match
  • Tuition reimbursement
  • Flexible work environment
  • Discretionary PTO (Paid Time Off)
  • Paid holidays
  • Medical, Dental, and vision coverage
  • HSA/FSA
  • Telemedicine (Virtual doctor appointments)
  • Wellness program
  • Adoption assistance
  • Short term disability
  • Long term disability
  • Life insurance
  • Discount programs

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