Clinical Research Associate - all levels at Parexel | GlassEver Jobs

Clinical Research Associate - all levels at Parexel | GlassEver Jobs

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Clinical Research Associate - all levels

Brazil Oct 22, 2026
Clinical-Research-Associate Clinical-Research-Coordinator Clinical-Trial-Monitor Clinical-Research-Associate-II Clinical-Research-Associate-Trainee Clinical-Research-Assistant Assistant-Clinical-Research-Associate Clinical-Trial-Associate Clinical-Trials-Associate Clinical-Research-Aide

Job Description

When our values align, there's no limit to what we can achieve.

At , 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 , 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 , 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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