Clinical Trial Monitor
1 dia atrás
Job Opportunity: Phase 2 Clinical Trials Monitor We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. This position involves collaborating with investigators, site personnel, and cross-functional teams to ensure the safety and well-being of participants in early-phase clinical trials. Our goal is to deliver high-quality results that meet the needs of our clients. Key Responsibilities Site Management and Monitoring Conduct site qualification, initiation, interim monitoring, and close-out visits. Ensure proper site adherence to protocols, GCP, and regulatory requirements. Verify and ensure accurate data collection and reporting. Assess site performance and provide corrective actions if necessary. Regulatory Compliance Ensure all clinical trial documentation is maintained according to regulatory guidelines. Review informed consent documents and confirm proper consenting procedures. Collaborate with regulatory teams to ensure timely submissions and approvals. Safety and Data Management Monitor and report adverse events (AEs), serious adverse events (SAEs), and dose‑limiting toxicities. Validate source data and resolve data discrepancies. Ensure timely and accurate documentation of clinical trial data in electronic data capture (EDC) systems. Collaboration and Communication Build and maintain relationships with study investigators and site staff. Communicate study updates and findings to study sponsors and internal teams. Provide training to site personnel on study protocols, procedures, and GCP compliance. Requirements Bachelor's degree in Life Sciences, Nursing, or a related field. At least 2-4 years of experience as a Clinical Research Associate in oncology trials, with preference for Phase 2 experience. Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and ICH guidelines. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS). Excellent organizational, problem‑solving, and communication skills. Preferred Qualifications Previous experience in early-phase oncology trials (e.g., dose escalation studies, first‑in‑human trials). Strong understanding of pharmacokinetics (PK) and pharmacodynamics (PD) assessments. Certification as a Clinical Research Professional (CCRA) is a plus. #J-18808-Ljbffr
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Clinical Trial Monitor
Há 5 dias
Porto Alegre, Brasil Bebeeclinicalresearch Tempo inteiroJob Opportunity: Phase 2 Clinical Trials MonitorWe are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage clinical trials.The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol.This position involves collaborating with...
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Clinical Trials Specialist
Há 2 dias
Porto Alegre, RS, Brasil beBeeClinicalResearchAssociate Tempo inteiroKey Responsibilities: Monitor and manage clinical trials. Ensure site compliance with regulatory requirements. Verify accurate data collection and reporting. Evaluate site performance and implement corrective actions as needed. About the Ideal Candidate: A Bachelor's degree in Life Sciences, Nursing, or a related field is required. At least 2-4 years of...
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Clinical Trials Coordinator
Há 3 dias
Porto Alegre, Brasil Bebeeepilepsy Tempo inteiroSenior Clinical Research Associate (CRA)This role supports a Phase II/III Epilepsy Study with regular site visits across the United States.Duration: 12 months with potential renewalExperience: At least 5+ years of independent monitoringTravel: Frequent site visitsTherapeutic Area: Neurology with strong desire for seizure trial experienceThe sponsor...
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Chief Oncology Clinical Trial Manager
Há 5 horas
Porto Alegre, RS, Brasil beBeeClinicalResearchAssociate Tempo inteiroWe are seeking a detail-oriented and experienced Clinical Research Associate to monitor and manage early-phase clinical trials. The successful candidate will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. This position involves collaborating with investigators, site personnel, and...
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Clinical Research Associate For Clinical Trials In Brazil
1 semana atrás
Porto Alegre, Brasil Bebeeresearch Tempo inteiroJob Overview:We are seeking a qualified Clinical Research Associate to support Phase 2 and 3 clinical trials in Brazil.As a key team member, you will lead site visits, monitor compliance, and ensure high-quality data.Your Responsibilities:Conduct site evaluations, initiations, monitoring & close-outsEnsure Good Clinical Practice (GCP) compliance and data...
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Clinical Trials Coordinator
Há 2 dias
Porto Alegre, RS, Brasil beBeeEpilepsy Tempo inteiroSenior Clinical Research Associate (CRA) This role supports a Phase II/III Epilepsy Study with regular site visits across the United States. Duration: 12 months with potential renewal Experience: At least 5+ years of independent monitoring Travel: Frequent site visits Therapeutic Area: Neurology with strong desire for seizure trial experience The sponsor...
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Contract Clinical Research Associate
1 dia atrás
Porto Alegre, Brasil Barrington James Tempo inteiroContract CRA Project - 40 hours per week 1 year contract. Seizure or Epilepsy - CNS Job Summary : We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 Seizure study clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and...
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Principal Data Scientist
Há 3 dias
Porto Alegre, Brasil Bebeeclinicaldatascience Tempo inteiroSenior Clinical Data Science ProgrammerAbout the Role:This is a pivotal position in developing and implementing programming solutions to support the analysis and reporting of clinical trial data.You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming...
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Principal Data Scientist
Há 2 dias
Porto Alegre, RS, Brasil beBeeClinicalDataScience Tempo inteiroSenior Clinical Data Science Programmer About the Role: This is a pivotal position in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming...
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Clinical Trial Nurse
1 semana atrás
Porto Alegre, Brasil IQVIA Tempo inteiro**Are you a Registered Nurse interested in Clinical Trial work?** IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting research, collecting data and samples to help evaluate safety/efficacy...
