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Parexel

Clinical Research Associate - Experienced II/Sr

Posted 9 days ago
0-2 years experience
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AI Summary

Monitor clinical trial sites through on-site and remote visits, maintain strong relationships with investigators and site staff, and collaborate with cross-functional teams to meet project timelines. Manage study documentation and visit reports, implement corrective actions when needed, and ensure sites remain audit- and inspection-ready.

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.

We are seeking experienced Clinical Research Associates (CRA) 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

  • 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; only candidates residing in São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre are eligible
  • Must be fluent in English and Portuguese
  • 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 would 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.


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