Clinical Trial Assistant Jobs in São Paulo

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Senior Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patie...

547792 - Clinical Trials AssistantMedical Oncology DepartmentCalvary Mater NewcastleTemporary (12months) Full-TimeEveryone is welcome at Calvary Mater NewcastleAs a Clinical Trials Assistant you will be responsible for processing of clinical trial research laboratory samples data entry for allocated...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

Purpose:Support development of public policies and regulations that are conducive for expansion of electronic paymentsSupport the raise and optimization of Visas profile and reputation through the delivery of coordinated communications and education targeted at key regulators government officials an...

Your Role:The Regulatory Affairs Manager BRAZIL  develops and executes regulatory strategies in alignment with Global and Affiliate Regulatory colleagues as appropriate. S/he represents Brazil  on the Global Regulatory Product Teams (GRPTs) and leads Area Regulatory Product Teams (ARPTs) to identify...

At Lilly we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them improve the understanding and man...

Your Role:The Regulatory Affairs Manager develops and executes regulatory strategies in alignment with Global and Affiliate Regulatory colleagues as appropriate. S/he represents Area on the Global Regulatory Product Teams (GRPTs) and leads Area Regulatory Product Teams (ARPTs) to identify and compil...

DescriptionRegulatory Affairs Manager LATAMLocation: São Paulo Brazil (Hybrid 3 days per week in the office)Hologic is a leading developer manufacturer and supplier of diagnostic products medical imaging systems and surgical products with a strong emphasis on serving the healthcare needs of women....

External Job DescriptionPerform 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 delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

About ConvatecPioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company focused on solutions for the management of chronic conditions with leading positions in Advanced Wound Care Ostomy Care Continence Care and Infusion Care....

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishBased in BrazilResponsibilitie...

Why Join UsBe a hero for our rare disease patientsAt Ultragenyx we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to achieve this goal our vision is to lead the future of rare disease medicine. For us this means goi...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Perform 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 delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accur...

The Lead Data Manager will be responsible for all data management activities in large complex studies under general supervision or working under minimal supervision on data management activities for small to medium sized projects.  CommunicationPrimary communication point for project teams and compa...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager/Clinical Lead - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager/Clinical Lead is accountable for achieving the final clinical deliverable (usually clean data from e...

Medical Writer - Senior Regulatory Writing Specialist (Clinical) Essentials: Degree: Advanced degree in a scientific discipline (eg life sciencespharmacy medicine) or relevant work experience;or equivalent combination of educationtraining and experience. Experience: At least 3 to 5 years as a Regula...