Note: The job is a remote job and is open to candidates in USA. Parexel is hiring Clinical Research Associates to support high-quality clinical trial execution, site partnerships, and compliance across study phases. The role monitors clinical trial sites, manages site-level documentation and reporting, and works with investigators, site staff, and cross-functional teams to maintain study integrity and inspection readiness.

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 when needed to maintain study integrity
• Ensure sites are always audit- and inspection-ready

Skills

• 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
• Must be fluent in English and Spanish
• Bachelor's degree in life sciences, pharmacy, nursing, or related field is required
• A minimum of 1 year of CRA experience required

Benefits

• Be part of groundbreaking projects pushing the boundaries of clinical research
• Work in a collaborative and inclusive environment that values your expertise
• Career growth and professional development opportunities
• Work-life balance and flexible working arrangements
• Home-based role

Company Overview

Company H1B Sponsorship