Clinical Site Technology Specialist

Overview Company Description 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 than2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines...

A leading biopharmaceutical solutions organization is looking for a Site Contracts Specialist. This role involves negotiating contracts and budgets for clinical trials, administering contract management processes, and collaborating with internal and external stakeholders. Candidates should possess moderate contract management experience, strong communication...

A global clinical research company is seeking a Site Technology Specialist in Buenos Aires, Argentina. This role involves providing technical support to clinical sites, assisting with technology-related documentation, and ensuring effective communication within project teams. Ideal candidates will have a Registered Nurse degree, at least 5 years of...

A leading global provider of clinical research services is seeking a Senior Regulatory and Start Up Specialist in Chubut, Argentina. The role entails performing site activation activities in compliance with local and international regulations, overseeing project timelines, and ensuring quality control of documents. Candidates must hold a Bachelor's degree in...

Site Contracts Specialist Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of...

Site Readiness and Regulatory Specialist I Job Overview Primary contact with investigative sites during study maintenance and, when assigned, site startup activities, responsible for collecting required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the agreed timelines with...

A global health care leader is seeking an experienced Clinical Research Associate in Argentina. This role involves ensuring compliance with ICH/GCP standards, managing research sites, and maintaining quality throughout all trial phases. Candidates should have a minimum of 2 years of experience in site management and a strong academic background in science or...

A leading global provider of clinical research services is seeking a Senior Site Activation Coordinator in Argentina. In this hybrid role, you will oversee site activation activities, support the preparation and approval of essential documents, and maintain project-specific systems. Ideal candidates will hold a Bachelor’s Degree in Life Sciences and have...

Job Overview Clinical Research Associate role at MSD LATAM – a global health care leader. The position is accountable for performance and compliance for assigned protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures,...

A leading biopharmaceutical solutions organization is seeking a Sr Investigator Management Solutions (IMS) Specialist to support clinical trial management in a hybrid model. The role involves analyzing site clinical trial agreements, ensuring budget accuracy, and collaborating with internal teams for project support. Candidates should have a Bachelor's...