
Senior Clinical Research Professional
1 dia atrás
The Clinical Research Associate II role is a key position in our organization, responsible for conducting site visits and serving as the site manager.
- Perform and coordinate clinical monitoring tasks in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures (SOPs) to assess investigational products and/or medical devices.
- Conduct site visits to determine protocol and regulatory compliance, preparing required documentation.
- Develop collaborative relationships with investigative sites and study vendors.
- Provide protocol and related study training to assigned clinical study sites.
Additional responsibilities include:
- Maintaining oversight of site performance by tracking metrics for enrollment, data entry into Case Report Forms (CRFs), protocol deviation trends, and overall site issues.
- Serving as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues.
- Communicating site performance to the Clinical Study Team (CST).
Key Responsibilities:
Site Management:
- Coordinate site visits and ensure compliance with GCPs and SOPs.
- Monitor site performance and address any issues that may arise.
Clinical Monitoring:
- Perform and coordinate clinical monitoring tasks to assess investigational products and/or medical devices.
- Conduct site visits to determine protocol and regulatory compliance.
Requirements:
- Strong communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Excellent organizational and time management skills.
Benefits:
This role offers a competitive salary and benefits package, as well as opportunities for professional growth and development.
-
Senior Clinical Research Professional
Há 3 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiroJob 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...
-
Senior Clinical Research Associate
Há 3 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$120.000 - R$170.000Senior 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...
-
Clinical Research Professional
Há 8 horas
São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro R$87.000 - R$109.000Are you a detail-oriented professional with a passion for research? As a Clinical Research Associate, your role will be to ensure the smooth conduct of clinical trials while maintaining high standards of data integrity and patient safety.About the RoleAs a Clinical Research Associate, you will be responsible for conducting site qualification and initiation...
-
Senior Clinical Research Professional
Há 3 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiroClinical Research Associate Job DescriptionThe role of a Clinical Research Associate (CRA) is to oversee the execution of clinical research projects in various settings, including offices and home-based environments. The CRA will work closely with project teams to ensure timely completion of tasks and maintain high-quality data integrity.Coordinate with...
-
Clinical Research Professional
Há 9 horas
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$150.000 - R$250.000Job OverviewThis position is an exciting opportunity to join a global clinical research organization. As a Clinical Research Associate, you will be responsible for managing investigator sites throughout the site lifecycle.
-
São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$60.000 - R$90.000Job Title:Senior Clinical Research AssociateJob Description:We are seeking a skilled and experienced Senior Clinical Research Associate to join our team. As a key member of our clinical research operations, you will be responsible for conducting site visits, managing study documents, and collaborating with project teams to ensure the successful execution of...
-
Senior Clinical Research Professional
Há 3 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiro US$80.000 - US$100.000Clinical Research Associate (CRA)The primary responsibility of a Clinical Research Associate (CRA) is to oversee clinical trials and ensure they are conducted in accordance with Good Clinical Practice (GCP) guidelines.About the RoleWe are seeking an experienced and detail-oriented CRA to join our team. The successful candidate will be responsible...
-
Senior Clinical Research Professional
Há 4 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiroAt ICON, we're seeking a talented Clinical Research Associate to join our diverse and dynamic team. As a key member of our team, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.The successful candidate will be responsible for...
-
Senior Clinical Research Associate
Há 2 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$50.000 - R$80.000Job OverviewWe are seeking an experienced Senior Clinical Research Associate to oversee and manage clinical trial activities. As a key member of our team, you will play a critical role in ensuring trials are conducted according to protocol, regulatory requirements, and industry standards.
-
Clinical Research Coordinator
Há 10 horas
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...