Clinical Research Monitor
Há 5 dias
As 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 Responsibilities- Monitor investigator sites with a risk-based approach, identifying site processes failures and implementing corrective actions to ensure compliance and reduce risks.
- Conduct on-site and remote monitoring activities, reviewing data accuracy through SDR, SDV, and CRF reviews as applicable.
- Assess investigational products through physical inventory and records review, documenting observations in reports and letters.
- Escalate observed deficiencies and issues to clinical management expeditiously, following up on findings as necessary.
To be successful in this role, you will need:
- A Bachelor's degree in a life science-related field or a Registered Nursing certification or equivalent.
- Previous experience providing knowledge, skills, and abilities comparable to 3+ years as a clinical research monitor.
- Valid driver's license where applicable.
We offer a range of benefits, including:
- Continued career advancement opportunities.
- Award-winning training programs.
- Benefits focused on employee health and wellbeing.
We are committed to helping our employees grow and develop in their careers. We offer:
- Mentoring and coaching opportunities.
- Training and development programs.
- Career advancement opportunities.
-
Clinical Research Professional
Há 21 horas
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$72.000 - R$108.000Job Opportunity: Clinical Research AssociateWe are seeking a skilled Clinical Research Associate to play a pivotal role in the successful execution of clinical trials. As a key member of our team, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor...
-
Clinical Research Associate
1 semana atrás
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$70.000 - R$95.000Clinical Research Associate Job Summary">Fortrea is a leading global contract research organization dedicated to delivering high-quality clinical development solutions. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical studies by monitoring and managing sites.">Main Responsibilities:">Conduct routine...
-
Clinical Research Professional
Há 6 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiro R$58.673 - R$86.285Clinical Research Associate Position OverviewWe are seeking an experienced and skilled Clinical Research Associate to join our team. As a key member of our team, you will be responsible for monitoring clinical research studies and ensuring the integrity of clinical data.
-
Clinical Research Professional
Há 7 dias
São Paulo, São Paulo, Brasil beBeeCRA Tempo inteiro R$90.000 - R$105.000**Job Title:** Clinical Research AssociateCareer Description:We are seeking an experienced and skilled Clinical Research Associate to join our team. As a CRA, you will be responsible for monitoring clinical studies to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.Key Responsibilities:Site Management: Verify study...
-
Clinical Research Specialist
1 dia atrás
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$65.000 - R$85.000Job Opportunity:We are seeking a skilled Clinical Research Professional to support the successful execution of clinical studies.Responsibilities:Monitor clinical investigative sites to ensure protocol execution and adherence to regulations, good clinical practices, and quality standards.Conduct site qualification, initiation, interim monitoring, and study...
-
Senior Clinical Research Associate
Há 5 dias
São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$90.000 - R$120.000Senior Clinical Research AssociateAs a Senior Clinical Research Associate, you will play a pivotal role in ensuring the successful execution of clinical trials. Your primary responsibility will be to oversee and conduct site initiation visits, monitor ongoing studies, and ensure compliance with regulatory requirements.Your expertise will be sought after to...
-
Senior Clinical Research Associate Leader
Há 22 horas
São Paulo, São Paulo, Brasil beBeeCareer Tempo inteiro R$134.465 - R$172.152We are seeking a highly motivated and organized Senior Clinical Research Associate Leader to join our team. In this role, you will be responsible for leading clinical research associates in the execution of clinical trials, ensuring compliance with regulatory requirements and good clinical practices.Key Responsibilities:Lead a team of clinical research...
-
Clinical Research Professional
Há 2 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$45.000 - R$75.000Job OverviewWe are seeking a highly skilled Clinical Research Associate to support our organization in the conduct of site visits, monitoring of site performance and implementation of action plans as needed.Main ResponsibilitiesConduct site visits and monitor site performance to ensure compliance with regulatory requirementsImplement corrective action plans...
-
Clinical Research Coordinator
1 semana atrás
São Paulo, São Paulo, Brasil beBeeClinicalMonitoring Tempo inteiro R$64.000 - R$86.000Clinical Monitoring SpecialistThe role of Clinical Monitoring Specialist is to oversee the implementation of clinical trials at designated sites. Key responsibilities include site management, monitoring data quality, and ensuring compliance with regulatory requirements.Key Responsibilities:Conduct site visits to monitor data collection and reportingReview...
-
Senior Clinical Research Coordinator
Há 7 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro US$85.000 - US$103.000Job SummaryClinical Research Program Manager oversees the development, coordination, and implementation of Phase 1 clinical research studies at various facilities.Key Responsibilities:Develop, coordinate, and implement study protocols in adherence to project timelines.Collaborate with principal investigators to design study protocols ensuring scientific...
