Clinical Research Coordinator

Pearl Pathways is a life science consulting company specializing in regulatory, quality compliance, and clinical services for biopharmaceutical, medical device, and diagnostic companies. Known as a trusted advisor, the company offers tailored solutions to expedite product development and navigate the complexities of regulatory environments. Pearl Pathways combines decades of clinical, scientific, and regulatory experience to support clients in achieving their business objectives.

Additionally, Pearl IRB, a full-service independent review board, enables comprehensive support for human research initiatives.

This is a 1099 role for a Clinical Research Coordinator, based in the Indianapolis, IN area. The Clinical Research Coordinator will oversee clinical trial activities, including obtaining informed consent, ensuring adherence to protocols, coordinating clinical research activities, and facilitating compliance with regulatory requirements. Responsibilities also include collaborating with internal and external stakeholders to ensure the successful execution of clinical trials while maintaining timelines and quality standards.

• Knowledge of Informed Consent processes and Protocol adherence
• Strong understanding of research processes, methodologies, and regulatory compliance
• Excellent organizational, communication, and interpersonal skills
• Problem-solving abilities and attention to detail
• Bachelor’s degree in a related field or relevant clinical research certification is preferred
• Experience in the GI therapeutic area preferred
• 3-5 years of experience with Clinical Research and Clinical Trials