Clinical Research Jobs in Valparaiso Ant
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Cra2 Santiago De Chile
Iqvia
Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...
Medical Advisor Dermatology & Gastroenterology Chi...
Abbvie
Represent the affiliates medical/scientific voice of expertise for assigned products and relevant indications in Dermatology & Gastroenterology. Provide medical / scientific expert advice / guidance to key customers for assigned products and relevant therapeutic areas including scientific exchange a...
Clinical, Medical, Regulatory And Quality Senior D...
Novo Nordisk
Clinical Medical Regulatory and Quality DepartmentSantiago ChileAre you passionate about driving medical innovation and ensuring regulatory compliance Do you have the expertise to lead multi-functional teams and make unordinary impact on patients lives If so we invite you to join Novo Nordisk as ou...
Clinical Project Manager, Iqvia Biotech
Iqvia
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.IQVIA Biotech is seeking an experienced Clinical Project...
Senior Research Manager
Nielseniq
In this Strategic Leadership Role you will be responsible for Customer Success for the Brand & Media Strategic Analytics & Insight Practice Area across Chile reporting into the SA&I Customer Success Brand & Media regional leader. Key responsibilities encompass delivering with excellence while mainta...
Assoc. Spclst., Regulatory Affairs
Msd
Job DescriptionBrindar apoyo en la preparación presentación y seguimiento de trámites regulatorios de productos veterinarios (medicamentos vacunas antiparasitarios productos biológicos) bajo la supervisión del responsable regulatorio. Asegurar el cumplimiento de la normativa nacional aplicable y man...
Clinical Regional Project Lead
Psi Cro
The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.Ensures planning implementat...
Lead Clinical Research Associate
Psi Cro
Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Moni...
Regional Project Lead
Psi Cro
The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.Ensures planning implementat...
Site Readiness And Regulatory Senior Specialist
Fortrea
Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made withi...
Client Services Rep
Iqvia
Job OverviewUnder guidance controls the report generation process and provides guidance and support to clients daily or as a specialist on specific products/services.Essential Functions Ensures the contract fulfillment to specifications of basic and routine reports for defined customers. Reviews cli...
Panel Administrator Associate
Iqvia
At IQVIA we are committed to using data and science to help healthcare clients find better solutions for their patients. As a Panel Administrator Associate youll be at the forefront of this missionengaging pharmacies and physicians to participate in critical healthcare research panels.What Youll DoM...
Site Readiness And Regulatory Specialist Ii
Fortrea
Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made withi...
Internal Medical Translator En > Esla /esus
Iqvia
RESPONSIBILITIES Be a strategic partner in delivering translations on time and adhering to our quality commitments to clients Carefully adhere to provided material and instructions to meet the requirements of the clients Research industry-specific terminology to properly reflect the meaning and tone...
Cra1 - Santiago De Chile
Iqvia
Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...
Rwe Cra 1
Chl Iqvia Rds Chile
Responsible for remote and on-sitemonitoring activities to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Serves as an in-house CRA responsible for site mana...