Clinical Research Associate - Experienced II/Sr

Parexel; Brasil; Remote; BRL 120.000 - 180.000; Vollzeit

Zusammenfassung

Parexel is seeking experienced Clinical Research Associates (CRAs) to monitor clinical trial sites through on-site and remote visits, build strong relationships with investigators and site staff, and collaborate with cross-functional teams to meet project timelines.

The role requires a bachelor’s degree in life sciences, pharmacy, nursing, or related field and a minimum of 1 year CRA experience. Fluency in English and Portuguese is required, with the role being home-based for Brazilian residents.

Qualifikationen

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field required.
• Minimum of 1 year CRA experience required.
• Fluency in English and Portuguese required.

Aufgaben

• 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.

Kenntnisse

Detail-oriented

Problem solving

Communication

Independent

Flexible working

Ausbildung

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

Jobbeschreibung

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.