
Clinical Site Quality Specialist
Há 6 dias
Job Summary:
This role involves managing site quality and delivery from site identification through close-out as the direct point of contact for clinical sites.
- Build relationships with sites to ensure successful initiation, patient recruitment, and compliance with regulations.
- Evaluate site efficacy, assess compliance, and develop strategies for improvement.
- Oversee trial conduct at designated sites, ensuring subject rights and data integrity.
The Clinical Research Associate will be responsible for:
- Managing site performance, including problem-solving and issue resolution.
- Developing and implementing patient recruitment strategies.
- Ensuring compliance with GCP and regulatory requirements.
To succeed in this role, you will need:
- Site management experience or equivalent experience in clinical research.
- A strong understanding of clinical trials methodology and terminology.
- Advanced communication and problem-solving skills.
This role offers a range of benefits, including:
- Opportunities for professional growth and development.
- A dynamic and supportive team environment.
- The chance to work on diverse projects and contribute to innovative solutions.
This is an exciting opportunity to join our team and make a meaningful contribution to the field of clinical research. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply.
-
Medical Site Quality Specialist
Há 7 dias
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro US$80.000 - US$120.000The role of a Clinical Research Associate involves acting as the primary point of contact for clinical sites, ensuring quality and timely delivery throughout the site identification to close-out process. Their primary goal is to establish strong relationships with the site, monitor its performance, and drive it towards successful...
-
Clinical Site Navigator
3 semanas atrás
São Paulo, São Paulo, Brasil Fortrea Tempo inteiroClinical Site Navigator (Start-up Specialist II) Join to apply for the Clinical Site Navigator (Start-up Specialist II) role at Fortrea Clinical Site Navigator (Start-up Specialist II) 1 day ago Be among the first 25 applicants Join to apply for the Clinical Site Navigator (Start-up Specialist II) role at Fortrea The Clinical Site Navigator role is a...
-
Clinical Site Management Specialist
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeNavigator Tempo inteiro US$55.000 - US$92.100Clinical Site Navigator RoleDeliver exceptional site management and regulatory compliance as a Clinical Site Navigator.This hybrid role combines start-up and iHCRA/CRA responsibilities to ensure seamless progression from feasibility to site activation, through maintenance phase as required.Coordinate site-level activities throughout the start-up phase of a...
-
Clinical Site Manager
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiro US$90.000 - US$120.000Clinical Research Associate RoleThe Clinical Research Associate plays a vital role in ensuring the quality and efficiency of clinical trial site management. They establish strong relationships with clinical sites, guaranteeing compliance with regulations and study requirements.Key Responsibilities:Manage site initiation, develop effective patient recruitment...
-
Clinical Quality Manager
Há 5 dias
São Paulo, São Paulo, Brasil Curebase Tempo inteiro**About the role**Curebase is seeking a Clinical Quality Manager who will thrive in a quickly scaling healthcare technology environment. The Quality and Compliance team at Curebase is deeply collaborative, and you will collaborate with Clinical Operations, while leading and mentoring the Clinical Quality team. This role reports directly to the Director of...
-
Clinical Trial Site Activation Coordinator
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeActivation Tempo inteiro R$50.000 - R$100.000Site Activation SpecialistWe are seeking a skilled and organized Site Activation Specialist to join our team. As a key member of our operations team, you will play a critical role in the successful activation of clinical trial sites.Key Responsibilities:Coordinate site activation activities for assigned studies, ensuring timely and accurate completion of...
-
Clinical Research Specialist
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$105.000 - R$145.000Job Title: Clinical Research SpecialistAs a clinical research specialist, you will play a vital role in advancing global healthcare through innovative research and development. Your expertise will be instrumental in ensuring the safety and efficacy of our products through rigorous clinical trials and surveillance.Key Responsibilities:Develops and maintains...
-
Senior Clinical Trials Specialist
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$90.000 - US$130.000Clinical Research Associate Role OverviewThe Clinical Research Associate plays a pivotal role in ensuring the integrity and quality of clinical trials. As a primary CRA, you will conduct site visits, manage relationships with key site personnel, and monitor data quality to ensure patient safety and compliance with regulatory guidelines.
-
Sr Clinical Site Navigator
3 semanas atrás
São Paulo, São Paulo, Brasil Fortrea Tempo inteiroSr Clinical Site Navigator (Senior Start-up Specialist) Join to apply for the Sr Clinical Site Navigator (Senior Start-up Specialist) role at Fortrea . Job Overview The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in coordinating site-level activities...
-
Senior Site Coordinator
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro US$58.400 - US$85.600Job Summary:We are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our clinical operations group, you will be responsible for managing site quality and delivery from site identification through close-out.This role involves building strong relationships with sites, overseeing trial conduct, ensuring subject rights and...