Senior Clinical Monitoring Analyst

Há 2 dias

São Paulo, São Paulo, Brasil beBeeAnalyst Tempo inteiro R$90.000 - R$115.500
Job Role

Sr Cm Analyst I

Job Overview

This role involves serving as the Centralized Monitoring functional lead, with expertise in RBQM methodologies, tools, and processes.

Key Responsibilities
  • Develop and implement centralized monitoring plans and generate findings reports.
  • Manage review timelines and oversee budget management.
  • Communicate effectively with the study team and ensure reviews are complete.
  • Lead Centralized Monitoring Review meetings to discuss issues and risks with the study team.
  • Contribute to risk assessment through department risk assessment tools and participate in cross-functional risk assessment review meetings.
  • Characterize and track evidence of issues, signals, and potential risks.
  • Provide training and mentorship to junior team members.
Requirements
  • Bachelor's degree or equivalent relevant formal academic qualification.
  • At least 5 years of experience in clinical monitoring, data management, biostatistics, or a related field in support of clinical trials.
Essential Skills
  • Strong organizational skills with adherence to regulatory guidelines and global SOPs.
  • Excellent attention to detail and numerical skills.
  • Proven analytical and problem-solving abilities.
  • Ability to work independently and within a team environment.
  • Effective oral and written communication skills.
  • Proficiency with MS Office and interactive computer systems.

  • Clinical Monitoring Associate

    Há 2 dias

    São Paulo, São Paulo, Brasil beBeeMonitoring Tempo inteiro R$80.000 - R$120.000

    Job DescriptionClinical trials rely heavily on the expertise of Clinical Research Associates. As a CRA II, you will be responsible for upholding the integrity and quality of clinical trial data.Key Responsibilities:Develop project plans related to Clinical Monitoring responsibilities.Ensure informed consent procedures and protocol requirements are adhered...

  • Oncology Clinical Monitoring Associate

    Há 2 dias

    São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro

    Oncology Clinical Monitoring Associate We are seeking an experienced and motivated professional to join our global clinical team as a Clinical Monitoring Associate. This role will be responsible for ensuring the integrity of clinical trials by conducting site visits, monitoring data quality, and maintaining relationships with key site personnel.Key...

  • Senior Clinical Research Professional

    Há 2 dias

    São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro

    Job DescriptionAs a Senior Clinical Research Associate, you will be responsible for managing site responsibilities for clinical studies according to Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) guidelines, and applicable project plans.Verify study training records and ensure compliance with SOPs, GCP, and regulatory requirements.Conduct...

  • Monitoring Intelligence Analyst

    Há 2 dias

    São Paulo, São Paulo, Brasil CloudWalk, Inc. Tempo inteiro

    Join to apply for the Monitoring Intelligence Analyst (Night Shift) role at CloudWalk, Inc. Join to apply for the Monitoring Intelligence Analyst (Night Shift) role at CloudWalk, Inc. Get AI-powered advice on this job and more exclusive features. About CloudWalk:CloudWalk is an AI-first fintech building its own technology to bring justice to the broken

  • Senior Clinical Research Associate

    Há 2 dias

    São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$120.000 - R$170.000

    Senior Clinical Research Associate RoleFoster innovation and excellence in clinical development by joining our dynamic team as a Senior Clinical Research Associate.About the RoleWe seek experienced professionals to conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.Evaluate and ensure protocol compliance, data...

  • Senior Oncology Clinical Research Professional

    2 semanas atrás

    São Paulo, São Paulo, Brasil beBeeOncology Tempo inteiro R$107.425 - R$142.050

    Job Title:Sr. Clinical Research AssociateOncology Expertise RequiredWe are seeking a highly experienced Senior Clinical Research Associate to lead site management and monitoring visits in the oncology field.About the Role:The ideal candidate will possess at least 2 years of on-site monitoring experience in oncology, with a strong background in clinical...

  • Clinical Research Associate

    4 semanas atrás

    São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    **Clinical Research Associate - São Paulo Brazil****(Level Depending on Experience)****Job Purpose/Summary**Completes project activities associated with monitoring functions of Phase I through Phase IV clinical research studies while continuing to develop knowledge of drug development process, ICH / Good Clinical Practice (GCP), and applicable local...

  • Senior Clinical Research Associate Role

    Há 2 dias

    São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiro

    Senior Clinical Research Associate OpportunityWe are seeking a seasoned Senior Clinical Research Associate to join our team in overseeing and managing clinical trial activities. As a Senior CRA, you will play a critical role in ensuring trials are conducted according to protocol, regulatory requirements, and industry standards.Key Responsibilities:Monitoring...

  • Clinical Data Analyst

    Há 3 dias

    São Paulo, São Paulo, Brasil beBeeRisk Tempo inteiro

    We are a dynamic, global company that cares for our staff, clients, and partners. Our mission is to bring together passionate individuals who drive quality work in the medical science field.Job DescriptionYou will join a team with a shared mentality and desire to develop smart and intelligent approaches to project monitoring. Your role will be to shape the...

  • Senior Clinical Trial Coordinator

    Há 2 dias

    São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$120.000 - US$140.000

    Job OpportunityThe primary responsibility of the Senior Clinical Research Associate will be to ensure that clinical trials are conducted in accordance with contracted scope of work and regulatory requirements.Key Responsibilities:Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with the study protocol and...