Clinical Trial Nurse Per Diem Porto Alegre, BR
1 semana atrás
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 of a new medication. The visits / hours can be arranged to suit your current work schedule but need to be in the morning / early afternoon. Preferably we look for PRN Nurses or Nurses who already work part time. Role of nurse during visit Collecting samples and required information and data Drawing blood Vitals Urine test Medication administration if needed Labelling and shipment of samples Reporting of adverse events Input reporting and event notes post assignment The task can vary depending on the trial Requirements Active RN license in home state Pediatric Nursing qualification and experience - nice to have BLS certification required Must be comfortable with basic software programs Recent experience in drawing blood Flexible with your time and available on short notice Ability to travel regionally by car Willing to travel up to 90 miles if needed Possess cellular phone reliable transportation and access to the internet Ability to stand for long periods of time bend or kneeling may be required You will have a flexible schedule an opportunity to travel grow and expand into new opportunities while earning supplemental income and gaining exposure to clinical trials. #LI-CES and #LI-DNP and #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Key Skills EMR Systems,Hospital Experience,Acute Care,ICU Experience,Dermal Fillers,Experience Administering Injections,Home Care,Nursing,Botox Experience,Critical Care Experience,Medication Administration,Tube Feeding Employment Type: Part-Time Experience: years Vacancy: 1 #J-18808-Ljbffr
-
São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroClinical Project Manager (Level Dependent on Experience) Join to apply for the Clinical Project Manager (Level Dependent on Experience) role at CTI Clinical Trial and Consulting Services. CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization (CRO) focused on the advancement of...
-
Clinical Trial Coordinator
Há 6 dias
São Paulo, São Paulo, Brasil MSD Brasil Tempo inteiro R$40.000 - R$80.000 por anoJob DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...
-
Clinical Trial Coordinator
4 semanas atrás
São Paulo, Brasil Merck Gruppe - MSD Sharp & Dohme Tempo inteiroJob Description Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable. The...
-
Clinical Trials Assistant
Há 5 dias
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$24.600 - R$46.120 por anoThis is a talent pool for people with disabilities. If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs.Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File...
-
Clinical Trial Coordinator
1 semana atrás
São Paulo, São Paulo, Brasil MSD Tempo inteiro US$40.000 - US$80.000 por anoJob DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...
-
Clinical Trial Coordinator
4 semanas atrás
São Paulo, Brasil Merck Tempo inteiroJob Description Under the oversight of the line‑manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non‑clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable....
-
Clinical Trial Coordinator
1 semana atrás
São Paulo, São Paulo, Brasil MSD Tempo inteiro US$40.000 - US$80.000 por anoJob DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...
-
Clinical Trial Coordinator
1 semana atrás
São Paulo, São Paulo, Brasil MSD Tempo inteiro US$40.000 - US$80.000 por anoJob DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...
-
Clinical Trial Coordinator
4 semanas atrás
São Paulo, Brasil MSD Malaysia Tempo inteiroJob DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...
-
Senior Clinical Research Associate
4 semanas atrás
São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroAbout CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is...
