Indtast nøgleord

Ansøgningsfrist: 2025-05-23

Sr Clinical Research Associate

Udgivet 2025-03-24

As a pharmaceutical support industry leader , UBC is devoted to empowering health solutions for a better tomorrow . We take pride in improving  patient outcomes and advancing healthcare.  At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.

Embark on a rewarding career journey with UBC as a Sr Clinical Research Associate! Grow your career while making a meaningful impact  on the world around you. UBC fosters a culture built on our Core Values of Collaboration, Conscientiousness, Curiosity, Compassion and Consultation. We believe in an inclusive workplace that fosters creativity.

If you are seeking a career that will challenge, inspire, and reward you, join us at UBC!

Specific job duties:

  • Thorough knowledge and application of project specific protocol.
  • Consistently completes on site monitoring in accordance with project specific timelines.
  • Consistently completes travel scheduling in accordance with project specific and UBC guidelines
  • Attends project team meetings, department meetings and minimum of monthly 1:1 with manager; responsible for content of these meetings.
  • Consistently completes site monitoring reports, confirmation/follow-up letters per UBC and/or client SOPs; signs, scans and/or provides to Clinical Site Specialist/Regulatory Document Specialist for filing in Trial Master File according to UBC and/or sponsor timelines requiring minimal corrections.
  • Ensures follow-up of site issues and action items per UBC/sponsor timelines.
  • Enters site visits, confirmation/follow-up letters and site monitoring reports into UBC’s Clinical Trial Management System.
  • Ensures completion of Call Log or Telephone Contact Report detailing communication with sites per protocol.
  • Monitors within Electronic Data Capture data entry, if applicable, and assists sites with Case Report Form resolution.
  • Completes Regulatory Binder and Investigational Product reconciliation.
  • Maintains regular contact with assigned sites per study requirements.
  • Consistently submits expense reports within UBC timelines; consistently follows UBC Travel Guidelines.
  • Consistently completes SOP review and documentation within requested timelines.
  • Consistently completes sponsor specific training and documentation within requested timelines
  • Assists PM and management team by being an Assess Instruct and Mentor leader A = Assess visit type, assess protocol specific and UBC SOP knowledge and assess individual’s ability to perform visit type independently. I = Instruct how to conduct visit, report/letter writing and manage issues and actions. M = Mentor team member by sharing tips/tricks/tools reviewing process prior to and after visit.
  • Assists management team by mentoring other Clinical Research Associates.
  • Assists with preparation and/or delivery of presentations for UBC Clinical Research Associate training, departmental training and/or sponsor specific training.
  • Desired Skills and Qualifications:

  • Bachelor’s degree – Life Science preferred or equivalent years of industry and monitoring experience
  • Minimum of 5 years experience in current role and / or related function
  • Minimum of 1 years experience at a Service Provider
  • Minimum of 3 years experience in Oncology trials and 1 year experience in Ophthalmology
  • Phase 1 experience required; solid tumor experience preferred
  • Thorough knowledge of medical terminology
  • Good written and verbal communication skills
  • Consistently meets or exceeds metrics for quality trip reports and letters
  • Consistently meets or exceeds metrics for completion of UBC and/or sponsor training with appropriate documentation
  • Ability to perform tasks in UBC’s Clinical Trial Management System, Electronic Data Capture System, Outlook and client specific systems (if applicable)
  • Thorough knowledge of International Conference on Harmonisaton, Good Clinical Practice guidelines, Code of Federal Regulations and UBC SOPs
  • Lignende job

    Udgivet: 2025-03-31
    • London
    Udgivet: 2025-03-31
    • Technopole de Sophia Antipolis