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 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.

- Conduct site qualification, initiation, interim monitoring, and close-out visits in accordance with study protocols, GCP, applicable regulations, and SOPs.
- Monitor study conduct, source documentation, informed consent, subject safety information, and CRFs to support patient safety and data quality.
- Assess and train site staff on protocol requirements and address compliance or study-related issues as needed.
- Ensure regulatory, ethics, and site documentation is complete, current, and appropriately maintained for the Investigator Site File and Trial Master File.
- Partner with sites to resolve data queries,



maintain timely data submission, and ensure appropriate safety-event reporting and follow-up.
- Oversee study materials and investigational product receipt, accountability, return, or destruction at assigned sites.
- Maintain regular communication with investigative sites and document monitoring activities and findings through clear, timely visit reports.
- Contribute input to protocols, CRFs, monitoring plans, and feasibility activities as requested.
- Support the assessment and training of other CRAs through accompanied site visits when appropriate.

Where You'll Work

This is a home-based Clinical Research Associate role supporting sites across Argentina. Candidates must reside within the territory to effectively support site visits and study activities. You will collaborate with sites, sponsors, and integral study teams while traveling to investigative sites approximately 6-10 days per month.

To best support our sites, we're seeking candidates who are based in Argentina. Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

What You'll Do

- Conduct site qualification, initiation, interim monitoring, and close-out visits in accordance with study protocols, GCP, applicable regulations, and SOPs.
- Monitor study conduct, source documentation, informed consent, subject safety information,



and CRFs to support patient safety and data quality.
- Assess and train site staff on protocol requirements and address compliance or study-related issues as needed.
- Ensure regulatory, ethics, and site documentation is complete, current, and appropriately maintained for the Investigator Site File and Trial Master File.
- Partner with sites to resolve data queries, maintain timely data submission, and ensure appropriate safety-event reporting and follow-up.
- Oversee study materials and investigational product receipt, accountability, return, or destruction at assigned sites.
- Maintain regular communication with investigative sites and document monitoring activities and findings through clear, timely visit reports.
- Contribute input to protocols, CRFs, monitoring plans, 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 fiv

📌 Clinical Research Associate II (Córdoba)
🏢 Worldwide Clinical Trials
📍 Córdoba