Senior Study Start-Up CRA | Clinical Trials

Overview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...

Senior Clinical Research Associate (CRA) Join to apply for the Senior CRA role at IQVIA. The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with...

Clinical Project Manager – Level Dependent on Experience CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the life‑cycle of development,...

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...

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....

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,...

Clinical Project Manager, IQVIA Biotech IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. We are seeking an experienced Clinical Project Manager based in Argentina...

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 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...

Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill,...