Clinical Research Associate II / Senior Clinical Research Associate - Remote

Overview

The Clinical Research Associate II/Senior Clinical Research Associate role at Parexel focuses on managing and monitoring clinical trials to ensure patient safety and quality execution.

In Short

• Responsible for site management and monitoring of clinical trials.
• Ensure compliance with Good Clinical Practices and relevant laws.
• Manage operational aspects of clinical trial activities.
• Facilitate communication between study teams and investigator sites.
• Monitor site-level adverse events and collaborate with Drug Safety Unit.
• Serve as point of contact for audits and drive corrective action plans.
• Work in a supportive role for various therapeutic areas.
• Contribute to the development of therapies benefiting patients.
• Preferred experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.
• Join a global team dedicated to improving health outcomes.

Requirements

• Bachelor’s degree in life sciences or equivalent.
• Minimum 3 years of experience in clinical research site monitoring.
• Extensive knowledge of clinical trial methodologies.
• Familiarity with ICH/GCP and FDA regulations.
• Experience in Oncology is preferred.
• Strong communication and interpersonal skills.
• Ability to manage multiple tasks and timelines effectively.
• Commitment to patient well-being and ethical standards.
• Ability to work independently and as part of a team.
• Willingness to travel as necessary for site visits.

Benefits

• Work with a global leader in clinical research.
• Opportunity to contribute to significant health outcomes.
• Supportive and collaborative work environment.
• Access to comprehensive training and development resources.
• Competitive salary and benefits package.
• Flexible working options available.
• Engagement in diverse therapeutic areas.
• Opportunities for career advancement.
• Be part of a mission-driven organization.
• Work with a talented and dedicated team.