Senior Clinical Research Coordinator
Há 5 dias
Job Overview We are seeking a highly skilled Clinical Research Associate to join our team. Key Responsibilities: Clinical trials require meticulous site qualification, initiation, interim monitoring, and close-out visits to ensure accurate data collection and reporting. The CRA will verify that all clinical trial documentation is maintained according to regulatory guidelines and that informed consent documents are properly reviewed. This role also involves monitoring and reporting adverse events, ensuring timely submissions and approvals from regulatory teams. Safety and data management are critical aspects of this position, including validating source data and resolving discrepancies in electronic data capture systems. Frequent communication with study investigators and site staff is essential for successful collaboration and project delivery. Required Skills and Qualifications: Bachelor's degree in Life Sciences or related field. At least 2 years of experience in clinical research or a related field. Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Familiarity with GCP and regulatory requirements. Proficiency in electronic data capture systems. Benefits: Competitive salary and benefits package. A dynamic and supportive work environment. Flexible work arrangements. Why Join Us? We offer a unique opportunity to work on cutting-edge projects, collaborate with experts in the field, and make a real impact in the lives of patients. If you are passionate about clinical research and want to be part of a talented team, we encourage you to apply.
-
Senior Clinical Research Coordinator
1 dia atrás
Curitiba, Brasil Bebeeclinicalresearch Tempo inteiroJob Overview We are seeking a highly skilled Clinical Research Associate to join our team. Key Responsibilities Clinical trials require meticulous site qualification, initiation, interim monitoring, and close-out visits to ensure accurate data collection and reporting. The CRA will verify that all clinical trial documentation is maintained according to...
-
Senior Clinical Research Coordinator
Há 3 dias
Curitiba, Brasil Bebeeclinicalresearch Tempo inteiroJob OverviewWe are seeking a highly skilled Clinical Research Associate to join our team.Key Responsibilities:Clinical trials require meticulous site qualification, initiation, interim monitoring, and close-out visits to ensure accurate data collection and reporting.The CRA will verify that all clinical trial documentation is maintained according to...
-
Senior Clinical Research Professional
4 semanas atrás
Curitiba, Brasil beBeeClinicalResearch Tempo inteiroClinical Research Associate Role Conduct site visits, qualify sites, initiate trials, manage study files and provide instructions to personnel. Verify participant protection by confirming informed consent procedures and protocol adherence. Evaluate data integrity and compliance with approved protocols, GCP and SOPs. Duties: Coordinate investigative site...
-
Contract Clinical Research Associate
2 semanas atrás
Curitiba, Brasil Barrington James Tempo inteiroSenior Clinical Research Associate (CRA) — Epilepsy Study (Phase II/III) I'm currently looking for experienced Senior CRAs to join an exciting Phase II/III Epilepsy Study with one of my key clients. This is a 1.0 FTE contract role supporting 6–8 sites across Brazil — and it's available for an immediate start. If you're someone who thrives in neurology...
-
Contract Clinical Research Associate
2 semanas atrás
Curitiba, PR, Brasil Barrington James Tempo inteiroSenior Clinical Research Associate (CRA) — Epilepsy Study (Phase II/III) I'm currently looking for experienced Senior CRAs to join an exciting Phase II/III Epilepsy Study with one of my key clients. This is a 1.0 FTE contract role supporting 6–8 sites across Brazil — and it's available for an immediate start. If you're someone who thrives in neurology...
-
Lead Clinical Trial Programmer
Há 3 dias
Curitiba, Brasil Bebeeclinical Tempo inteiroSenior Clinical Data Science Programmer Job DescriptionAs a Senior Clinical Data Science Programmer, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data.Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, data review/risk...
-
Lead Clinical Trial Programmer
Há 5 dias
Curitiba, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer Job Description As a Senior Clinical Data Science Programmer, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, data review/risk...
-
Epilepsy Study Specialist
2 semanas atrás
Curitiba, Brasil beBeeNeurology Tempo inteiroSenior Clinical Research Associate Position This is an exciting opportunity to join a dynamic team in support of a Phase II/III Epilepsy Study. As a Senior Clinical Research Associate, you will be responsible for monitoring and managing clinical trials at 6–8 sites across Brazil. The ideal candidate will have extensive experience in independent monitoring,...
-
Research Analyst
Há 2 dias
Curitiba, Brasil Pulse Labs Tempo inteiroPulse Labs is empowering insights and elevating experiences for the world's top technology companies. Backed by investors including Google and Amazon, we're revolutionizing product development delivering human-centered, actionable insights at every stage of the product lifecycle from inception to market release and beyond. We empower top tech companies to...
-
Clinical Data Science Program Lead
2 semanas atrás
Curitiba, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer This role involves developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Develop, validate, and maintain programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. Collaborate...
