## Clinical Research Associate II - ArgentinaApply: Remote: Buenos Aires, Argentina: Full time: Posted Today: JR******Join a integral 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 world. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. **Make an Impact as a Clinical Research Associate at Worldwide** As a Clinical Research Associate, you'll play a key role in protecting patient safety and data quality throughout the clinical trial lifecycle. You'll work closely with investigative sites to ensure studies are conducted in line with protocols, Good Clinical Practice (GCP), applicable regulations, and study requirements.You'll take ownership of site qualification, initiation, interim monitoring, site management, and close-out activities. Through strong site relationships, effective monitoring, and timely follow-up, you'll help ensure reliable study data and successful study delivery.This role gives you the opportunity to apply your clinical research expertise across multiple therapeutic areas while collaborating with sites and study teams. ## Where You'll WorkThis is a home-based Clinical Research Associate role supporting sites across Argentina.





and feasibility activities as requested.* Support the assessment and training of other CRAs through accompanied site visits when appropriate. ## What You'll Bring * Education and experience: MD or Pharmacy degree (MSPH, PharmD, PhD, or equivalent) with at least one year of experience as a Clinical Research Associate Level I; OR a four-year degree focused on medical, biological, physical, health, pharmacy, or a related science with at least two years of clinical research experience; OR a two-year college curriculum or equivalent education/training, preferably nursing or life sciences, with two years of experience as a Clinical Research Associate Level I.* Strong knowledge of clinical research principles and processes, GCP, ICH Guidelines, applicable FDA and/or EU regulations, local regulatory requirements, and SOPs.* Clinical research knowledge across three to five therapeutic areas, or in-depth knowledge of two to three therapeutic areas.* Proficiency with Microsoft Office, IxRS, and electronic data capture (EDC) systems.* Excellent communication, organisation, time-management, interpersonal, initiative, and problem-solving skills, with the ability to work independently in an organised and methodical way.* Proficiency in spoken and written English, together with fluency in the local languages of the countries under responsibility.* Valid current passport and driving licence, with willingness to travel as required.* Experience in full-service monitoring PREFERRED **Discover the Difference** We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit ** or connect with us on**LinkedIn**.
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? Clinical Research Associate II - Argentina (Buenos Aires)
? Worldwide
? Buenos Aires

📌 Clinical Research Associate Ii Argentina (Buenos Aires)
🏢 Empresa líder
📍 Buenos Aires