Hybrid Senior Site Activation Specialist

A leading biopharmaceutical solutions organization in Argentina is seeking a Senior Site Activation Manager to oversee the Site Start-Up deliverables. The successful candidate will manage site activities from selection to activation, ensuring compliance with regulations and timely delivery. The ideal candidate has a strong background in project management...

Join to apply for the Senior Site Activation Coordinator role at IQVIA. Make an impact on patient health! Hybrid – Argentina Job Overview As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities. These activities will be in accordance with applicable local...

Join to apply for the Senior Site Activation Manager hybrid Argentina role at Syneos Health . 2 days ago – Be among the first 25 applicants. 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...

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...

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...

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...

FSP - Sr. Regulatory and Start Up Specialist Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities....

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...

Clinical Site Technology Specialist (Nuclear Medicine) 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,...

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...