clinical data associate

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the...

## Clinical Research Associate II - ArgentinaApply: Remote: Buenos Aires, Argentina: Full time: Posted Today: JR103297Join a global Contract Resource Organization (CRO) where innovation meets purpose. At **Worldwide Clinical Trials**, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPurpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors...

ICON Strategic Solutions is seeking a Study Start Up Associate I in Argentina to support site start-up and activation for clinical trials. You will collaborate with cross-functional teams to ensure regulatory compliance and timely study initiation, contributing to innovative therapies that benefit patients worldwide.The role emphasizes detailed regulatory...

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the...

Use Your Power for PurposeWork Location Assignment: Buenos Aires, Argentina (Complejo LUMINA - Office Park). This role follows a hybrid model. Colleagues are expected to work from the assigned Pfizer office 2-3 days per week, or as required by business needs.Our mission is straightforward: support healthcare decisions that ensure the safe and effective use...

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and...

Job Description Our 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,...

Merck & Co., Inc. in Rahway, NJ, USA seeks an Associate Director, Data Collection Data Steward to oversee program-level data standards within GDMS/GCDS. Lead Therapeutic Area Standards Teams, train staff, and support information governance across the clinical lifecycle.You will guide data definitions (EDC and non-EDC), ensure harmonization with CDISC and...

Fortrea is seeking a Site Monitoring Specialist to oversee clinical study sites and manage site activities. You will ensure proper initiation, conduct visits, and maintain study files while safeguarding patient safety and data integrity.The role requires coordination with sponsors, adherence to SOPs, and efficient travel; English fluency and regulatory...

Buenos Aires ThermoFisher Scientific is seeking an entry-level Clinical Research Associate I (FSP CRA I) to join the monitoring team in Buenos Aires. The role involves coordinating site activities, performing remote or on-site visits, and ensuring protocol and regulatory compliance according to ICH-GCP for multiple sponsors and trial environments.You will...

Fortrea is seeking a Regulatory Affairs professional to act as the primary site liaison, ensuring timely collection and submission of essential documents for EC/IRB/Regulatory Authority approvals. You will support in-country regulatory activities, maintain compliant study documentation, and coordinate with vendors to meet global requirements.Experience with...

Parexel is seeking a Milestone One Site Coordinator in Mendoza, Argentina to support trial sites in line with ICH-GCP and protocol timelines. You will serve as the primary liaison between Sponsor/CRO and the site, ensuring timely responses and smooth monitoring visits.Responsibilities include tracking enrollment, maintaining site documents, supporting budget...

Join . Morgan in Buenos Aires and take the next step in your career by leading and driving a high-performing team. As a CRG Associate, you’ll collaborate with teams across North America, oversee the delivery of high-impact financial analysis and research, and ensure the success of client meetings and live transactions. We value experienced, analytical...

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II / Senior CRA at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.You will conduct...

Caraway Therapeutics, Inc. in Argentina is seeking a Clinical Research Associate to manage and monitor study sites, ensuring ICH-GCP compliance and effective site operations. You will oversee site performance, regulatory documentation, and collaboration across sponsor teams to advance trials in the region.The role requires 2 years of direct site management...

Syneos Health is seeking a Senior CRA I to perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory compliance and data integrity. The role may involve on-site or remote activities with up to 75% travel.You will support source data verification, IP handling, and coordination with site staff. Knowledge of ICH/GCP...

Thermo Fisher Scientific is seeking a Clinical Research Associate I to support monitoring and site management across trials, ensuring protocol and regulatory compliance.You will conduct remote or on-site visits, manage essential documents per ICH-GCP guidelines, and collaborate with sponsors and investigational sites to guarantee patient safety and data...

Clinical Trials Associate - Argentina - Mexico - BrazilWe use cookies to improve your browsing experience and help us improve our websites. We have carefully selected third parties that use cookies to achieve purposes illustrated in the cookie policy. For more information. Read more about online privacy statement. By closing this banner or continuing to...

Syneos Health Argentina S.A. is seeking a CRA to perform site qualification, initiation, monitoring and close-out visits, ensuring regulatory adherence and data integrity.The role may involve on-site or remote activities with a focus on protocol compliance and patient safety. Responsibilities include overseeing informed consent, site file accuracy, and data...