Biotech Jobs In Argentina - 212 Job Positions Available

IQVIA Biotech is hiring for Sr. Site Contracts Associate in with 3-5 years experience negotiating clinical site contracts and budget templates. Grant Plan a plus. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25

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

Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level

Assoc. Medical Director This Assoc. Medical Director role will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a

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.

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 DescriptionJoin Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than

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