Clinical project manager

Há 2 dias

São Paulo, São Paulo, Brasil Caderno Nacional Tempo inteiro
Segmento: Não Informado

Atividades:

The Clinical Project Manager I is expected to require support and guidance from Directors and/or advanced Clinical Project Management (CPM) staff in the management of the essential functions of the CPM role listed below.

What You'll Do
  1. Plan, implement, evaluate, and complete full execution of assigned clinical trials; with support of assigned trial Director
  2. Set goals and timelines, provide oversight and foster motivation within the team to accomplish goals within the defined timelines and with high quality in the execution of assigned clinical trials
  3. Provide oversight and coordination of the operational aspects of the functional areas on assigned projects to ensure compliance with ICH guidelines, GCP, applicable regulatory guidelines, and trial procedures
  4. Manage full scope clinical trial projects from start-up through analysis phase, including oversight of team members on clinical trials; may handle multiple projects simultaneously
  5. Implement project activities according to scope of contracted work
  6. Coordinate clinical trial projects, including organization, implementation, and management of scoped activities
  7. Develop trial plans and timelines; work with trial Directors to address challenges during the project
  8. Participate in or oversee the development of trial deliverables
  9. Serve as a client contact at the operational level
  10. Oversee contracted vendors, review specifications, and ensure timelines and expectations are met
  11. Track project progress using computer-assisted programs, ensuring timely data entry and accurate reporting
  12. Monitor resource needs and communicate with department heads
  13. Ensure training for the clinical trial team for effective protocol implementation
  14. Oversee CRA tasks, site management, and data monitoring
  15. Review and approve site reports, escalate issues as needed
  16. Attend site visits as needed for observation or support
  17. Manage project budget and scope, working with the Director for corrective actions and scope changes
  18. Lead meetings for effective communication and decision-making
  19. Prepare project status reports
  20. Plan Investigator meetings and develop related materials
  21. Maintain and audit the Trial Master File (TMF)
  22. Participate in business development activities as requested
What You Bring
  • Bachelor's degree or equivalent, preferably in health-related fields
  • At least 3 years research experience in clinical trials or related transferable skills
Why CTI?

- Support for career progression with promotion opportunities and mentoring

- Valuing education and training, including tuition reimbursement

Dias da Semana: Não Informado

Horário / Período: Não Informado

Os interessados devem se candidatar através do portal Caderno Nacional
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