Clinical Research Coordinator: Curitiba, Brazil

SAO Fortrea Brazil Limitada Clinical Trials AssistantWe are seeking a highly motivated and organized Clinical Trials Assistant to join our team in Fortrea, Brazil.About the JobThe Clinical Trials Assistant will be an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. This role will involve performing...

Job SummaryWe are seeking a highly skilled Clinical Research Project Coordinator to join our team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring timely delivery of tasks and maintaining high accuracy standards.Key Responsibilities Engage in clinical trial management on a day-to-day level Work closely...

Job SummaryWe are seeking a highly skilled Clinical Research Project Coordinator to join our team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring timely delivery of tasks and maintaining high accuracy standards.Key ResponsibilitiesEngage in clinical trial management on a day-to-day basisWork closely...

Company DescriptionAt PSI, we strive to deliver quality and on-time services across various therapeutic indications.**Job Overview**:We are seeking a skilled Clinical Research Project Coordinator to join our international team. As a key support to clinical research projects, you will streamline communication, maintain systems, and manage documents &...

Medpace is a full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are seeking a highly skilled Clinical Research Coordinator to support...

Role OverviewWe are seeking a highly skilled Clinical Research Coordinator to join our team at ICON. As a key member of our site management team, you will be responsible for ensuring the smooth execution of clinical trials.Key ResponsibilitiesDevelop and maintain a thorough understanding of ICON's SOPs, ICH GCP guidelines, and relevant regulations.Ensure...

Job SummaryClinical Trial Services, Inc. is seeking a highly skilled Clinical Research Associate Lead to join our team. As a Clinical Research Associate Lead, you will be responsible for overseeing the conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and providing guidance to site staff.Key...

About the JobWe are seeking a highly skilled Clinical Trial Assistant to join our team at ICON. As a Clinical Trial Assistant, you will play a key role in the management and coordination of clinical trials.Responsibilities:Recruitment and Site Management: Perform site feasibility assessments, negotiate agreements, and ensure accurate tracking and...

Job Overview:The Clinical Trials Assistant is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Clinical Trials Assistant shall reflect their experience, and level of contribution which they can make to the project.Key Responsibilities:Document and track...

Clinical Research Excellence at CTI Clinical Trial Services, IncWe maintain a culture of excellence across all regions by ensuring our remote employees are fully engaged. To achieve this, we hold weekly all-staff meetings. Each department provides an update on their study or milestone progress. Additionally, our employees can participate in one of our CTI...

Unlock a Career in Clinical ResearchWe are seeking a skilled and dedicated Clinical Trial Coordinator to join our team at Thermo Fisher Scientific. As a Clinical Trial Coordinator, you will play a crucial role in the success of our clinical trials, working closely with our clients to ensure timely and efficient project delivery.About the RoleThis is a...

Clinical Research Associate Job DescriptionAt Thermo Fisher Scientific, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of clinical trials. Your primary focus will be on monitoring and managing clinical trials, ensuring compliance...

Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...

Job SummaryWe are seeking a highly skilled Clinical Research Project Coordinator to join our team in clinical trial management. As a key member of our team, you will be responsible for coordinating projects from start to finish, ensuring timely delivery and high accuracy.About the RoleThe successful candidate will have a Bachelor's degree in a health...

As a leading global contract research organization (CRO), SAO Fortrea Brazil Limitada provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.Job Overview:Clinical Team Leads (CTLs) own the clinical delivery of clinical...

As a leading global contract research organization (CRO), SAO Fortrea Brazil Limitada provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.Job Overview:Clinical Team Leads (CTLs) own the clinical delivery of clinical...

Job Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Intrials Clinical Research. As a Regulatory Affairs Specialist, you will be responsible for managing regulatory and start-up activities for clinical trials in Latin America.Key Responsibilities:- Manage regulatory and...

Project Management AnalystAs a Project Management Analyst at IQVIA, you will play a crucial role in the delivery of clinical trials, working closely with clinical teams to improve patients' lives by bringing new drugs to the market faster. You will provide support to Project Leaders and Clinical Project Managers, helping to mitigate risk, control costs,...

**Job Overview**As a Clinical Research Associate, you will be responsible for ensuring the proper conduct of clinical trials at assigned sites. This includes performing site monitoring visits, administering protocol training, and evaluating the quality of study site practices.**Key Responsibilities:**Perform site monitoring visits to ensure compliance with...

Job Title: Regulatory Affairs At Intrials Clinical Research, we are seeking a highly skilled and experienced Regulatory Affairs professional to join our team.Primary Responsibilities:Manage the Regulatory & Study Start-up team in all aspects, with support from the Regulatory and Study Start-up Manager (RSM).Support RSM in defining metrics and KPIs for the...