Regulatory Documents Jobs in Brazil

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Func...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974 the...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionWe are currently seeking a Regulatory Affairs Specialistin Brazil to join our Regulatory Affairs department focused on local submissions. This is a fantastic opportunity to further develop your regulatory career and expertis...

Job DescriptionClinical Research Associate IIAre you passionate about clinical research and eager to make a significant impact in the healthcare industry We are looking for a dedicated Clinical Research Associate III to join our this role you will be the primary site contact throughout all phases o...

Home-based position in São PauloOnly CVs in English will be consideredWe are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer mentor and leader. We are committed to develop our employees in their car...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsStanding for full shiftJob DescriptionSummarized Purpose:Provides administrative and technical support to the Project Team. Supports audit readiness by ensuringfiles are reviewed according to the schedule detailed in the organizations SOP and de...

Job Overview:Accountable for the execution and oversight for the delivery of all services within an FSP model in line with the current Clinical Service Agreement (CSA). Responsible to ensure high quality performance for optimal service delivery. Responsible for providing instructions and direction o...

For our customer Selectchemie AG we are looking for a QA & RA Specialist (100 % workload)Workplace: Sao Paulo BrazilAbout Selectchemie AGSelectchemie is an independent Swiss company serving the pharmaceutical and nutrition industry since 1969 as a premier supplier of high quality ingredients and gen...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...