Empleos remotos: Salud

• Tiempo completo
• 10+ años de experiencia

AgileEngine, an Inc. 5000‑ranked software leader serving Fortune 500 brands and innovative startups, is seeking a senior Software Architect to evaluate and redesign the architecture of an FDA‑regulated SaaS product. The role demands deep expertise in mixed‑technology stacks…

Santiago del Estero, Santiago del Estero, Argentina

• Tiempo completo
• 0-2 años de experiencia

Join Worldwide Clinical Trials, a global CRO of 3,500+ experts, as a Remote Clinical Data Associate II based in Argentina. You’ll ensure the accuracy, completeness and integrity of clinical trial data through cleaning, review, testing and documentation, supporting study execution…

Buenos Aires, Argentina

• Tiempo completo
• 10+ años de experiencia

Worldwide Clinical Trials, a global CRO of 3,500+ experts, seeks a Manager, Clinical Data Management based in Argentina. This remote leadership role will direct data‑management teams and study portfolios, ensure project delivery and budget compliance, and serve as the main…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

We are Worldwide Clinical Trials, a global midsize CRO dedicated to innovative, high‑quality clinical research. We are seeking a remote Clinical Data Manager based in Argentina to lead data‑management activities across complex global studies, ensuring data accuracy, integrity…

Buenos Aires, Argentina

• Tiempo completo
• 0-2 años de experiencia

One World Global Services is hiring remote Spanish interpreters to facilitate real‑time communication between Spanish‑ and English‑speaking clients. The role requires fast, accurate language processing in a quiet home office, with opportunities for full‑time or part‑time shifts…

Mendoza, Mendoza, Argentina

• Tiempo completo
• 2-5 años de experiencia

EDETEK is looking for a Manager of Clinical Data Management to lead a remote team across Argentina, Brazil, and Mexico. You will oversee data management projects, ensure high‑quality clinical data delivery, and act as the primary liaison with clients and internal teams. The role…

Argentina

• Tiempo completo
• 0-2 años de experiencia

Thermo Fisher Scientific is seeking a Country Approval Associate to support the preparation, review, and coordination of country‑specific regulatory and ethics submissions. The role works under guidance to align local submissions with global strategy, coordinate with internal…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Thermo Fisher Scientific seeks a Senior Clinical Research Associate (Level I) to join its global clinical monitoring team. In this role you will conduct remote and on‑site visits, ensure protocol and regulatory compliance, and manage documentation across investigational sites…

Buenos Aires, Argentina

• Tiempo completo
• 0-2 años de experiencia

Join Thermo Fisher Scientific as a Clinical Research Associate (Level II) and work on global clinical trials supporting top pharmaceutical and biotech companies. You will perform remote and on‑site monitoring, ensure protocol and regulatory compliance, and collaborate with…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Thermo Fisher Scientific seeks a Senior Clinical Research Associate (Level II) to join its global team and drive clinical monitoring across investigator sites. In this role you will conduct on‑site and remote visits, ensure protocol, ICH‑GCP and regulatory compliance, and manage…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Thermo Fisher Scientific seeks a Senior Clinical Research Associate (Level I) to lead risk‑based monitoring of oncology/hematology trials across global sites. You will conduct on‑site and remote visits, ensure compliance with ICH‑GCP and sponsor SOPs, and drive data accuracy and…

Buenos Aires, Argentina

• Tiempo completo
• 0-2 años de experiencia

Join Thermo Fisher Scientific as a Country Approval Associate and support the preparation, review and coordination …

Argentina, Santiago del Estero, Argentina

• Tiempo completo
• 2-5 años de experiencia

Thermo Fisher Scientific is seeking a Site Contract Specialist to join its global team supporting leading pharma and biotech clients. In this role you will draft, review, negotiate and finalize study site agreements, manage budget and risk, and coordinate with internal functions…

Argentina, Santiago del Estero, Argentina

• Tiempo completo
• 0-2 años de experiencia

Thermo Fisher Scientific is seeking an Associate Site Contract Specialist to join its global team supporting pharmaceutical and biotech clients. In this role you will draft, negotiate, and finalize site contracts and budgets, coordinate with internal teams, and help drive timely…

Argentina, Santiago del Estero, Argentina

• Tiempo completo
• 5-10 años de experiencia

Candidates must hold a bachelor's degree or equivalent and possess at least 5 years of relevant experience in contract management. A detailed understanding of contract law, investigator grant budgets, and the pharmaceutical development process is required.

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Candidates must hold a bachelor's degree in a life sciences field or a Registered Nursing certification. At least one year of experience as a clinical research monitor is required, along with a valid driver's license.

Buenos Aires, Argentina

• Tiempo completo
• 5-10 años de experiencia

The Chemistry Manufacturing Controls (CMC) Manager will support global regulatory CMC strategies for small‑molecule products at Syneos Health, a leading life‑sciences services organization. The role involves preparing and reviewing CMC submissions, providing regulatory guidance…

Argentina

• Tiempo completo
• 2-5 años de experiencia

Thermo Fisher Scientific seeks a Country Approval Specialist to join its global team, managing and coordinating local regulatory submissions across ministries of health, ethics committees and special national applications. The role supports site start‑up activities, provides…

Buenos Aires, Argentina

• Tiempo completo
• 2-5 años de experiencia

Candidates must have at least 3 years of experience in clinical project management or a related field. A high school diploma is required, with an associate degree or higher preferred, along with a strong understanding of clinical trial regulations like GCP.

Argentina

• Tiempo completo
• 5-10 años de experiencia

IQVIA seeks a Medical Data Review Manager specialized in rheumatology to work remotely on a global scale. The role involves reviewing structured clinical patient data for plausibility, protocol adherence, and completeness, ensuring readiness for subsequent review stages…

Buenos Aires, Argentina