Description Reporting to the Manager, Medical Monitoring, Medical Affairs, the Medical Monitor Associate, provides medical, scientific, and administrative support to the medical monitoring team in their study level, department level, and cross-functional level activities. The Medical
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine: IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors.
Career CategoryClinical Development Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Associate Medical Director – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on
ROLE SUMMARY As part of the Clinical Data Collection Strategies (CDCS) group, an integral delivery unit within the Clinical Development Information Sciences (CDIS) organization, the Database Analyst is responsible for the programming of high-quality clinical databases. Responsible
Pharmacovigilance Medical Writing Manager Position Summary The Pharmacovigilance Medical Writing Manager is responsible for writing and editing a variety of scientific and medical content, including but not limited to the following: Aggregate Reports, Risk Management
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description To be revised by TA Join Us as an Associate Medical Director – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Database Analyst (Associate)-Clinical Data Collection Strategies page is loaded# Database Analyst (Associate)-Clinical Data Collection Strategieslocations: Argentina - Remote: Latin America - Any Pfizer Sitetime type: Voltijdsposted on: Vandaag geplaatstjob requisition id: ROLE SUMMARY As part of the Clinical
CRA 2, Argentina, IQVIA Biotech page is loaded# CRA 2, Argentina, IQVIA Biotechlocations: Buenos Aires, Argentinatime type: Full timeposted on: Posted Todayjob requisition id: R *IQVIA Biotech is now hiring for CRA 2 with a minimum of 1
We’re expanding our capabilities across Latin America , and we’re hiring a Senior Clinical Research Associate to support critical studies across Argentina! As a Senior CRA youll posses a wide-ranging and broad experience handling our most
We’re expanding our capabilities across Latin America , and we’re hiring a Senior Clinical Research Associate to support critical studies across Argentina! As a Senior CRA youll posses a wide-ranging and broad experience handling our most
IQVIA HCPN has an exciting position in Argentina for a freelance CRAs. Location: Argentina, travel within Argentina required FTE: 0.6 FTE Contract: Freelance Start: asap Duration: around 6 months Trials: Phase II Ophtalmology Basic Functions: Participates
Pharmacovigilance Medical Writing Manager Position Summary The Pharmacovigilance Medical Writing Manager is responsible for writing and editing a variety of scientific and medical content, including but not limited to the following: Aggregate Reports, Risk Management Plan(RMP), Risk
Pharmacovigilance Medical Writing Manager Position Summary The Pharmacovigilance Medical Writing Manager is responsible for writing and editing a variety of scientific and medical content, including but not limited to the following: Aggregate Reports, Risk Management Plan(RMP),
At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology. OpenEye, Cadence Molecular Sciences – a division of Cadence Design Systems – is an industry leader
PLEASE SUBMIT YOUR RESUME IN ENGLISH The Project Coordinator II provides coordination and operational support for site activation and maintenance activities across all study phases. This role demonstrates greater autonomy and ownership, with accountability for assigned
Reporting to the Manager, Medical Monitoring, Medical Affairs, the Medical Monitor Associate , provides medical, scientific, and administrative support to the medical monitoring team in their study level, department level, and cross-functional level activities. The Medical
When our values align, theres no limit to what we can achieve. Parexel FSP is looking for a Clinical Laboratory Study Manager. The candidate can be based anywhere in Argentina, Brazil, and/or Mexico. The Clinical Laboratory