Senior Clinical Research Associate

• Manage research activities at sites participating in Worldwide’s clinical research projects
• Identify potential sites to participate in research efforts
• Perform study start-up activities, including collecting regulatory documents from sites
• Support negotiation of contracts and budgets
• Train sites to collect data properly and report potential safety-related events
• Manage site activities during study maintenance
• Close down research activities at sites after study completion
• Conduct study initiation visits (SIVs)
• Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to detail
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS, and EDC Systems
• 5+ years of experience as a Clinical Research Associate
• 4-year university degree OR Nursing Degree
• Experience in Oncology is required
• Fluent in written and verbal English required
• Candidates must reside in Argentina
• Willingness to travel regionally required

• Diverse and inclusive work environment
• Supportive and cohesive teams
• Accessible leadership
• Opportunities for professionals from diverse backgrounds and experiences to succeed
• Equal employment opportunities
• Regional travel opportunities