Clinical Research Associate II - Remote Opportunity

About the Role

We are seeking a Clinical Research Associate II remote to join our Multi-Sponsor Clinical Operations Team at Parexel. This role offers a unique opportunity to contribute to improving the world's health by ensuring the success of clinical trials. As a Clinical Research Associate II remote, you will be the key point of contact for clinical sites, ensuring they are set up for success while maintaining high standards of quality and compliance.

What You'll Do

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites, generating detailed visit/contact reports.
• Build and maintain strong relationships with clinical site staff, addressing and resolving any site issues that arise.
• Review trial performance at designated sites to ensure the rights and well-being of human subjects are safeguarded in accordance with protocols.
• Develop patient recruitment strategies in collaboration with clinical sites to meet enrollment timelines while ensuring compliance with all regulatory requirements.
• Evaluate the quality and integrity of reported data, ensuring drug accountability and site efficacy.
• Monitor completeness and quality of regulatory documentation and perform site document verification.

Requirements

• Site Management or equivalent experience in clinical research, with a solid understanding of clinical trial methodology and terminology.
• Ability to perform all clinical monitoring activities independently.
• Bachelor’s or equivalent degree in biological science, pharmacy, or another health-related discipline.
• Strong interpersonal, written, and verbal communication skills within a matrixed team environment.
• Experience working in a self-driven capacity with a sense of urgency and limited oversight.
• A client-focused approach with a flexible attitude towards assignments and new learning opportunities.
• Ability to manage multiple tasks and evaluate unpredictable scenarios while meeting project timelines.
• Strong computer skills, including knowledge of Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), and MS Office products.

Nice to Have

• Experience in multiple therapeutic areas.
• Knowledge of Good Clinical Practice (GCP) guidelines.
• Previous experience in a remote working environment.

What We Offer

• Competitive salary and bonus incentive program.
• World-class technology and training tailored to your experience.
• Opportunities for career advancement in clinical research.
• Flexible working arrangements with less travel compared to industry standards.
• A supportive and collaborative work environment focused on patient care.