tmf

Precision for Medicine is seeking a Senior Regulatory and Start Up Specialist (Argentina) to lead regulatory and site start-up activities in the region. The role involves preparing submissions to Competent Authorities and Ethics Committees, adapting Informed Consent Forms, and ensuring on-time approvals for clinical trials.You will collaborate with CA/EC,...

Precision Medicine Group is hiring a Senior Clinical Research Associate to support studies in Argentina, with remote work options. The role involves start-up, on-site monitoring, site management, and mentoring of junior staff, ensuring patient safety, data integrity, and regulatory compliance.The ideal candidate has 5+ years as a CRA, strong GCP/ICH...

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job...

Job Title and Summary TMF Quality Project Manager or Records Management Analyst (Full home-based LATAM) Location Buenos Aires, ArgentinaSão Paulo, BrazilBogotá, Colombia Employment Type Full time, Remote Company Indero Company Culture At Indero, we are a contract research organization specializing in dermatology and rheumatology. Founded in 2000, our...

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery. The...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a FSP clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a FSP clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our...

Job Overview The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Project Coordinators (PC) are the right-hand support to the Project Lead. The Project Coordinator-I performs the essential duties with a large...

Job OverviewThe mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Project Coordinators (PC) are the right-hand support to the Project Lead. The Project Coordinator-I performs the essential duties with a large...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global...

Clinical Files Specialist - Entry Level role Work modality: Hybrid Job Overview 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...

Senior Regulatory and Start Up Specialist (Argentina) Remote, Argentina We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru , and we’re hiring our first Senior Regulatory and Start Up Specialist (Senior RSS) in Argentina! As the Senior RSS on our team, you are a seasoned, experienced professional in regulatory and...

Bei Roche kannst du ganz du selbst sein und wirst für deine einzigartigen Qualitäten geschätzt. Unsere Kultur fördert persönlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du für das, was du bist, wertgeschätzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl persönlich als auch beruflich wachsen kannst....

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global...

## CRA 2, ArgentinaApplylocations: Buenos Aires, Argentinatime type: Full timeposted on: Posted Todayjob requisition id: R1540400***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...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Clinical Research Manager (CRM) - home...

## In-House Clinical Research Associate I / II - Spanish / English / Portuguese (Argentina /Brazil)Apply: Remote: Buenos Aires, Argentina: Full time: Posted Today: JR103245Join a global Contract Resource Organization (CRO) where innovation meets purpose. At **Worldwide Clinical Trials**, we're driven by a shared commitment to improving lives...

LocationArgentina RemoteLanguage RequirementFluent English is RequiredPreferred ExperiencePharmaceutical/Biotech IndustryGeneral DescriptionThe Director Global Clinical Operations Compliance builds, collaborates and manages key relations to better support and understand the compliance-related needs of the business and drive the compliance activities within...