Empleos remotos: Ciencia e investigación

• Tiempo completo
• 5-10 años de experiencia

The Senior Clinical Research Associate I (Sr. CRA I) at Syneos Health will conduct site qualification, initiation, monitoring, and close‑out activities for clinical and real‑world studies, ensuring compliance with ICH‑GCP, GPP, and protocol requirements. The role demands strong…

Argentina

• Tiempo completo
• 5-10 años de experiencia

Candidates must hold a Baccalaureate degree with at least 7 years of relevant experience, or an advanced degree with at least 5 years of experience. Mastery of a specialty area and strong knowledge of industry practices are required for this individual contributor role.

Buenos Aires, Argentina

• Autónomo
• 2-5 años de experiencia

Summa Linguae Technologies (DATAmundi.ai) seeks a Talent Specialist to source and onboard contributors for complex, niche AI and data‑collection projects. The role focuses on hard‑to‑reach participants such as rare‑language speakers, specialized professionals, and unique…

Argentina

• Tiempo completo
• 2-5 años de experiencia
• US$ 60.000-119.000 / año

Join Worldwide Clinical Trials as a Specialist, Site Contracts and play a key role in advancing clinical research. You’ll lead the preparation, negotiation, and execution of site agreements, ensuring efficient study start‑ups while maintaining regulatory and contractual…

Argentina

• Tiempo completo
• 5-10 años de experiencia

The Site Contracts Specialist at Syneos Health will manage multi‑country site agreements and budget negotiations for industry‑sponsored clinical trials in Argentina, Chile, and Mexico. The role involves creating, reviewing, and executing site contracts, collaborating with legal…

Argentina

• Tiempo completo
• 2-5 años de experiencia

UniTriTeam is seeking a proactive Clinical Research Project Manager to own the end‑to‑end study start‑up and site activation process for its clinical research clients. In this remote, full‑time role you will coordinate cross‑functional teams, drive timelines, and ensure all…

Buenos Aires, Argentina

• Tiempo completo
• 0-2 años de experiencia

Clinical Data Coordinator I - Argentina Join ICON Strategic Solutions, the world’s largest FSP organization, in a sponsor‑dedicated model that leverages global expertise. You’ll support clinical trial design and analysis, handling complex medical data to help bring innovative…

Buenos Aires, Argentina

• Tiempo completo
• 0-2 años de experiencia

Join Worldwide Clinical Trials, a global CRO dedicated to high‑quality clinical research, as a Clinical Trials Associate working remotely from Argentina, Mexico, or Brazil. In this role you will support project teams by handling administrative and project‑tracking tasks, ensuring…

Buenos Aires, Argentina

• Tiempo completo
• 5-10 años de experiencia

Indero, a specialized CRO in dermatology and rheumatology, seeks a Project Manager II to own the full life‑cycle of multi‑site clinical trials—from initiation through closure. You’ll act as the main liaison with sponsors, drive project planning, budget control, and risk…

Buenos Aires, Argentina

• Tiempo completo
• 5-10 años de experiencia

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Argentina

• Media jornada
• 2-5 años de experiencia

Indero busca un/a Accounting Clerk (a tiempo parcial, de lunes a viernes) para apoyar las operaciones contables y financieras diarias de la entidad argentina. El/la candidato/a será responsable de conciliaciones, pagos a proveedores, preparación de flujo de caja mensual, soporte…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Join PSI CRO’s LatAm team as a Site Budget Specialist I, supporting clinical research start‑up activities from a home‑based position in Argentina. You will review and negotiate site budgets and contracts, collaborate with legal and project teams, and ensure proper documentation…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Join PSI CRO’s Latin America team as a Site Contract Specialist I, supporting clinical research start‑up activities from a home‑based position in Argentina. You will review and negotiate site budgets and contracts, collaborate with legal and project teams, and ensure proper…

Buenos Aires, Argentina

• Autónomo
• 0-2 años de experiencia

Join RWS TrainAI’s short‑term freelance project as an AI Voice Recording Contributor for Arabic (Jordan). Work from home, 4‑6 hours a day for about a month, earning $6 per hour while helping shape the next generation of speech‑AI. You’ll record native‑dialect text prompts using…

Salta, Salta, Argentina

• Tiempo completo
• 5-10 años de experiencia

Parexel is seeking a Clinical Laboratory Study Manager (CLSM) in Argentina to lead precision‑medicine sample and data operations. The role partners with study teams, data management, logistics and laboratory groups to ensure high‑quality biosample collection, tracking, testing…

Argentina, Santiago del Estero, Argentina

• Tiempo completo
• 2-5 años de experiencia

Worldwide Clinical Trials is seeking an In‑House Clinical Research Associate (I/II) to support site management across the study lifecycle for projects in Argentina or Brazil. This remote role works closely with Clinical Trial Managers, field CRAs, and study sites to ensure…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Codera, a Tang Capital life‑sciences company, is seeking a Site Director, Clinical Operations in Argentina to lead clinical site management for Phase I‑IV studies. The role oversees site identification, start‑up, monitoring, recruitment, and close‑out, ensuring compliance with…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

IQVIA is seeking a senior Site Activation Specialist, ICF Lead to manage country‑level site activation activities across LATAM on a home‑based work model. You will serve as the single point of contact for assigned studies, ensuring compliance with local regulations, SOPs and…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Candidates must hold a bachelor's degree in life sciences, medicine, pharmacy, nursing, or a related field. Proficiency in MS Office, knowledge of Good Clinical Practice (GCP) guidelines, and strong organizational skills are required.

Argentina

• Tiempo completo
• 0-2 años de experiencia

Join ICON Strategic Solutions as a Study Start Up Associate I in Argentina, where you’ll help launch clinical trials within a sponsor‑dedicated model. You’ll work closely with internal and external stakeholders to prepare regulatory submissions, activate sites, and support study…

Buenos Aires, Argentina