Clinical Training Coordinator

Há 15 horas


São Paulo, São Paulo, Brasil beBeeNursing Tempo inteiro R$90.000 - R$120.000

Job Summary:

We are seeking a skilled Nurse to join our team in São Paulo. The successful candidate will be responsible for managing key responsibilities related to education, training, policies, procedures, guidance, and communication.

Key Responsibilities:
  • Ensure compliance with d. ACADEMY nursing courses as per Diaverum policies.
  • Provide comprehensive onboarding and practical training for new employees, evaluated by clinic mentor nurses.
  • Support ongoing education based on Diaverum's Education norms.
  • Maintain accurate documentation of training courses.
Training Development and Evaluation:
  • Develop strategies to enhance clinic-based training with chief nurses.
  • Evaluate training program effectiveness and recommend improvements.
  • Ensure online training courses are updated in collaboration with the Nursing Director.
  • Provide updated academic resources and specialized nursing information.
Policies, Procedures, and Guidance:
  • Collaborate with the Nursing Director in translating policies and updating procedures.
  • Conduct audits and ensure compliance with the Annual Audit Plan.
  • Support chief nurses in conducting internal audits.
  • Ensure mentors efficiently fulfill their roles and responsibilities.
Communication and Support:
  • Facilitate effective communication among all stakeholders.
  • Promote evidence-based practice and encourage participation in clinical research.
  • Promptly report training issues and non-compliance to the Nursing Director and Chief Nurse.
  • Support multidisciplinary care standards and patient-centered philosophies.
Requirements:
  • Bachelor's degree in Nursing
  • Specialization in Hemodialysis
  • Minimum of four years' experience in Hemodialysis and two years' experience in nursing training, preferably in hemodialysis.

Learn more about this opportunity and how to apply:



  • São Paulo, São Paulo, Brasil beBeeStudy Tempo inteiro R$44.423 - R$65.491

    Job DescriptionThe Clinical Study Coordinator will be responsible for the setup, organization, and maintenance of clinical study documentation. This includes preparation for internal/external audits, final reconciliation, and archival.This role requires an ability to travel as needed, with at least 60% of the time dedicated to this activity. The coordinator...


  • São Paulo, São Paulo, Brasil beBeeTraining Tempo inteiro R$80.000 - R$150.000

    Job Title: Training CoordinatorOverviewWe are seeking a skilled and experienced training coordinator to join our team. The ideal candidate will have a strong background in training and development, with experience in coordinating training programs, developing curriculum, and documenting training records.ResponsibilitiesCoordinate training programs, including...


  • São Paulo, São Paulo, Brasil beBeeTraining Tempo inteiro R$45.000 - R$55.000

    Role SummaryWe are seeking a Clinical Training Specialist to join our team in São Paulo. As a key member of our renal care organization, you will be responsible for managing education, training, and compliance initiatives.


  • São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro

    Job DescriptionThe successful candidate will be responsible for coordinating all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures. This role involves being a decision-maker, solving problems independently or as part of the client and ICON team.Key...


  • São Paulo, São Paulo, Brasil beBeeNursing Tempo inteiro R$64.194 - R$83.749

    Clinical Training SpecialistDiaverum is seeking a skilled Clinical Training Specialist in São Paulo to oversee the education, training, and compliance of nurses.About the Position:The successful candidate will be responsible for managing key responsibilities related to education, training, policies, procedures, guidance, and communication at Diaverum. Key...


  • São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$65.000 - US$85.000

    Job Summary:Clinical Research Coordinator IAssists in the management of clinical trials by coordinating site initiation, monitoring, and close-out activities.Ensures compliance with regulatory requirements, including Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) Guidelines.Maintains a working knowledge of GCP guidelines,...


  • São Paulo, São Paulo, Brasil beBeeClinicalTrial Tempo inteiro R$37.678 - R$59.883

    Job OpportunityWe are seeking a highly skilled and experienced Clinical Trial Coordinator to join our global Clinical department.Key ResponsibilitiesProvide administrative and technical support to the Project Team, ensuring seamless collaboration and effective communication.Contribute to audit readiness by reviewing files on schedule as outlined in the...


  • São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro R$96.332 - R$126.596

    About the RoleAs a Clinical Research Monitor - Site Coordinator, you will play a critical role in ensuring the success of clinical trials by monitoring investigator sites and coordinating all aspects of the clinical monitoring process.Key ResponsibilitiesMonitor investigator sites with a risk-based approach, identifying site processes failures and...


  • São Paulo, São Paulo, Brasil BZL IQVIA RDS Brasil Ltda Tempo inteiro

    Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company that offers experience and supports career progression, with flexible working options? If so, join us - IQVIA is looking for a Clinical Research Coordinator.This role has an immediate start, working 40 hours a week for a period of 4 months to support...


  • São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$45.679 - R$64.343

    Job Overview:">Clinical Trial Assistant 1Perform daily administrative tasks in conjunction with the Clinical Research Associates and Regulatory teams to ensure a complete and accurate trial master file delivery.">Essential Functions">">Assist Clinical Research Associates (CRAs) and Regulatory teams with updating and maintaining clinical documents and systems...