Regulatory & Site Activation Lead - Clinical Trials

A leading global provider of clinical research services is seeking a part-time Site Research Assistant to work on-site in Ciudad Autónoma de Buenos Aires. The role involves providing support for clinical trials, including data entry, patient education, and managing study files. Candidates should possess a High School Diploma, with at least one year of...

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...

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 leading global clinical research company is seeking a Senior Clinical Research Associate (CRA) in Chubut, Argentina. The role involves planning, executing, and managing clinical trials to ensure data integrity and regulatory compliance. Candidates must have a Bachelor's degree in a relevant field and at least 4 years of on-site monitoring experience....

A global clinical research organization is seeking an experienced Clinical Project Manager in Argentina to lead innovative clinical trials in Immuno-Oncology and Cell and Gene Therapy. This role involves managing timelines, budgets, and ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor’s degree in Life Sciences and at...

Site Research Assistant, part-time (CABA) This is an on-site position in Ciudad Autónoma de Buenos Aires, part-time and fixed-term. Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies....

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 clinical research organization is seeking a Clinical Project Manager to oversee clinical trials in Neuquén, Argentina. The ideal candidate will have a Bachelor's degree in allied health fields and at least 6 years of clinical research experience. Responsibilities include project management from planning to execution, ensuring compliance with...

Clinical Regional Project Lead 3 days ago Be among the first 25 applicants. PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on‑time services across a variety of therapeutic indications. Job...

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...