Clinical Research Associate - all levels

Parexel; São Paulo; Hybrid; BRL 60,000 - 100,000; Full time

Job summary

Parexel is seeking experienced Clinical Research Associates (CRAs) to join a fast-paced team. This home-based role requires monitoring sites via on-site and remote visits, building strong investigator relationships, and collaborating with cross-functional teams to meet project timelines.

The CRA will manage site documentation, implement corrective actions when needed, and ensure audit readiness. Candidates must be fluent in English and Portuguese, hold a life sciences degree, have at least 1

Qualifications

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

Responsibilities

• 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 to maintain study integrity.
• Ensure sites are audit- and inspection-ready.

Skills

Detail-oriented

Problem solving

Communication

Collaboration

Adaptability

Independent worker

Remote/On-site support

Education

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

Job description

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

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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