Clinical Research Associate- all levels

Parexel; Argentina; À distance; ARS 1 000 000 - 1 400 000; Plein temps

Résumé du poste

Parexel is seeking an experienced Clinical Research Associate to join a fast-paced team focused on high-quality clinical trial execution. This home-based role supports virtual and in-person teams, emphasizing site monitoring, investigator relationships, and ensuring study integrity.

The ideal candidate holds a life sciences degree, has at least 1 year of CRA experience, and is fluent in English and Spanish. Occasional travel and a valid driver’s license are required.

Qualifications

• Bachelor's degree in life sciences, pharmacy, nursing, or related field.
• Minimum 1 year of CRA experience.
• Fluent in English and Spanish.
• Willingness to travel and hold a valid driver's license.

Responsabilités

• Monitor clinical trial sites through on-site and remote visits.
• Build and maintain strong relationships with investigators and site staff.
• Collaborate with cross-functional teams to meet project timelines.
• Manage site-level study documentation, systems updates, and visit reports.
• Implement corrective actions when needed to maintain study integrity.
• Ensure sites are audit- and inspection-ready.

Connaissances

Attention to detail

Problem solving

Communication

Collaboration

Independent work

Formation

Bachelor's degree in life sciences / pharmacy / nursing or related field

Description du poste

We are seeking experienced Clinical Research Associates to join our team. As a CRA, you'll be joining a fast-paced, driven environment that is helping to make a life-changing difference to patients by ensuring high-quality clinical trial execution, building strong site partnerships, and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams, CRAs are provided with multiple opportunities to excel and discover where their skills can take them.

Who We're Looking For

• Detail-oriented and a strong problem solver
• Highly communicative, collaborative, and adaptable
• Motivated, accountable, and able to work independently
• Positive, professional, and comfortable supporting virtual and in-person teams

What You'll Do

• Monitor clinical trial sites through on-site and remote visits
• Build and maintain strong relationships with investigators and site staff
• Collaborate with cross-functional teams to meet project timelines
• Manage site-level study documentation, systems updates, and visit reports
• Implement corrective actions when needed to maintain study integrity
• Ensure sites are always audit- and inspection-ready

Additional Details

• Home-based role; preference for candidates residing in Buenos Aires
• Must be fluent in English and Spanish
• Bachelor's degree in life sciences, pharmacy, nursing, or related field is required
• A minimum of 1 year of CRA experience required
• Must be able to travel and hold a valid driver's license

Why Join Us

• Be part of groundbreaking projects pushing the boundaries of clinical research
• Work in a collaborative and inclusive environment that values your expertise
• Unlock career growth and professional development opportunities
• Enjoy work-life balance and flexible working arrangements

If this job doesn't sound like your next step, but you know someone who'd be a perfect fit, feel free to share this opportunity with them!

At Parexel, we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and you're exposed to a world of experiences and open doors.