PA
ParexelClinical Research Associate II or Sr- Argentina
LocationArgentina-Remote
Also inBuenos Aires
Work moderemote
Typefull-time
SeniorityMid
Experience1+ yrs
Company size10,000+ people
PostedSep 18, 2026 · 3w ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
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
Must be fluent in English and Spanish
Bachelor's degree in life sciences, pharmacy, nursing, or related field
A minimum of 1 year of CRA experience
Must be able to travel and hold a valid driver's license
Benefits
Work life balance
Flexible working
When our values align, there’s no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.
About the role
At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing medicines to patients. We are seeking an experienced Clinical Research Associate II/Sr to join our team. As a CRA, you’ll be joining a fast‑paced, driven environment that’s 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
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Detail‑oriented and a strong problem solver
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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
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Monitor clinical trial sites through on‑site and remote visits
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Build and maintain strong relationships with investigators and site staff
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Collaborate with cross‑functional teams to meet project timelines
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Manage site‑level study documentation, systems updates, and visit reports
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Implement corrective actions when needed to maintain study integrity
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Ensure sites are always audit- and inspection-ready
Additional Details
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Home‑based role; preference for candidates residing in Buenos Aires
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Must be fluent in English and Spanish
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Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
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A minimum of 1 year of CRA experience required
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Must be able to travel and hold a valid driver’s license
Why Join Us
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Be part of groundbreaking projects pushing the boundaries of clinical research
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Work in a collaborative and inclusive environment that values your expertise
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Unlock career growth and professional development opportunities
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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.