Life Science Jobs in Argentina

Viseven Group is a leading global B2B MarTech service provider empowering Pharma and LifeScience companies since 2009. Our mission is to drive digital transformation and excellence offering comprehensive end-to-end software and digital marketing services tailored to the pharmaceutical industry. The...

About Beeline Medicines:Beeline Medicines is a clinicalstage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-dis...

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and ancillary start-up...

Job Overview:Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensu...

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...

Job OverviewUnder general supervision perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also inclu...

Job Overview:Document Review Specialist I is responsible for reviewing Investigator Packages Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP FDA and other regional guidance. Document Review Specialist I is responsible for reviewing revi...

Make an impact on patient health!IQVIAs Global Site Activation Team of 2000 employees drives best in class site and customer experience with industry leading outcomes.We keep the patient at the forefront; Always Impatient for the Patient and we excel in our collaboration with our external/internal c...

ROLE SUMMARYAs part of theClinical Data Collection Strategies (CDCS) group an integral delivery unit within theClinical Development Information Sciences (CDIS)organization the Database Analystis responsible forthe programming of high-quality clinical for supporting assigned segments of the Pfizer...

ROLE SUMMARYAs part of theClinical Data Collection Strategies (CDCS) group an integral delivery unit within theClinical Development Information Sciences (CDIS)organization the Database Analystis responsible forthe programming of high-quality clinical for supporting assigned segments of the Pfizer...

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensures...

Job OverviewAccountable for capability and learning activities related to the delivery of CDGM services and the adoption of TMF and good documentation practices across the business.ResponsibilitiesDevelop and implement effective fit-for-purpose capability development learning and knowledge managemen...

Job Overview:Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensu...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOffice Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on...

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...

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensures smo...

Job Overview.Direct and manage the execution of the strategic operational and financial delivery of required Site Activation activities including but not limited to Site ID and Selection Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company scope of work...