Parexel is Seeking a Clinical Research Associate II in São Paulo

At Parexel, our mission is clear: we work to get life-changing treatments to patients sooner. At the very heart of this mission are our Clinical Research Associates (CRAs). We are currently searching for a dedicated and experienced Clinical Research Associate II in São Paulo, Brazil, to join our world-class team.

This isn’t just a monitoring role; it’s an opportunity to take ownership of site relationships, ensure the highest standards of patient safety, and contribute to global projects across a wide variety of therapeutic areas.

Role at a Glance

For those who want the key details first, here’s a snapshot of the position:

• Job Title: Clinical Research Associate II
• Job ID: R0000034632
• Company: Parexel
• Location: São Paulo, Brazil
• Required Experience: Proven experience in clinical site management or an equivalent CRA role.
• Education: University degree (life sciences, pharmacy, or related discipline is preferred).
• Travel Required: Yes, this role requires extensive travel to investigator sites.

The Role: A Pivotal Partner in Clinical Research

As a Clinical Research Associate II, you will serve as Parexel’s direct point of contact for assigned clinical sites. Your primary responsibility is to ensure the complete integrity of the study’s implementation, championing adherence to the protocol and prioritizing the well-being of every patient. You will be empowered to build strong relationships, solve complex problems, and act with unwavering integrity.

Your Core Responsibilities

Your role will be dynamic, encompassing the full lifecycle of a clinical site from initiation through close-out.

Site Management & Relationship Building

• Serve as the primary liaison, building and nurturing strong, collaborative relationships with investigators and their site staff.
• Conduct comprehensive on-site and remote monitoring visits, including qualification, initiation, routine, and close-out visits.
• Proactively identify site needs, providing targeted training and resources to ensure compliance and engagement.
• Continuously evaluate site performance and recruitment strategies, providing expert recommendations for improvement.

Clinical Monitoring & Data Integrity

• Perform rigorous monitoring to ensure adherence to the study protocol, ICH-GCP guidelines, and all applicable regulations.
• Apply your expertise to identify and evaluate potential issues with data quality and integrity, implementing corrective actions to resolve them swiftly.
• Diligently follow up on CRF data entry, query resolution, and Serious Adverse Events (SAEs) to ensure timely and accurate reporting.
• Manage the accountability of the test article/study supply at the site level.

Compliance & Quality Assurance

• Ensure that your assigned sites are always audit and inspection-ready.
• Meticulously collect, review, and maintain all essential site documentation, ensuring the Trial Master File (TMF) is complete and of the highest quality.
• Act as a subject matter expert on ICH-GCP and local regulations, guiding your sites toward full compliance.

What You Will Bring: The Profile of Success

We are looking for a professional who combines deep clinical research knowledge with exceptional interpersonal skills.

Essential Experience & Education

• A university degree, preferably in a biological science, pharmacy, or other health-related discipline (or equivalent nursing qualification/experience).
• Proven experience in site management or an equivalent role within clinical research, demonstrating a strong understanding of clinical trial methodology and terminology.

Key Skills for Success

• Autonomous Problem-Solver: You possess strong analytical skills and the ability to take initiative, work independently, and make confident decisions to resolve site issues.
• Exceptional Communicator: You have strong interpersonal, verbal, and written communication skills, with the ability to interact professionally with clients and site staff.
• Highly Organized & Detail-Oriented: You have a keen eye for detail and the ability to prioritize multiple tasks to meet project timelines in a dynamic environment.
• Collaborative Team Player: You thrive in a matrix environment, value the importance of teamwork, and are committed to performing consistently high-quality work.
• Tech-Savvy & Adaptable: You are proficient with clinical trial systems (CTMS, EDMS, EDC) and MS Office, and you have a flexible attitude toward new technologies and work assignments.

Why Build Your Career at Parexel?

Choosing to be a CRA at Parexel means choosing to be part of something bigger. You will join a diverse global team with a wealth of experience, working on projects that have a direct impact on public health. We are deeply invested in your personal and professional growth, offering structured career paths, ongoing training, and opportunities to become a subject matter expert.

Our culture is built on collaboration, mutual support, and a shared commitment to quality. You will be encouraged to be curious, to challenge the status quo, and to take ownership of your work. If you are ready to make a tangible difference in the lives of patients and grow your career with a global leader, we want to hear from you.

Ready to Join Our Mission?

Take the next step in your professional journey. Apply today to become a pivotal part of the Parexel team in São Paulo.

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