Clinical Project Coordinator

BD; United States; Remote; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Clinical Project Coordinator to ensure the success of clinical studies within the Peripheral Intervention business unit. This role is crucial in delivering high-quality support and ensuring compliance with global clinical procedures and regulations. The ideal candidate will manage the operational aspects of clinical studies, including study supplies and administrative support, while upholding the highest standards of scientific integrity and ethics. If you're passionate about clinical research and looking to make a meaningful impact, this opportunity is perfect for you.

Qualifications

• Experience in managing clinical studies with a focus on compliance and quality.
• Strong understanding of regulatory guidelines and GCP.

Responsibilities

• Manage day-to-day operations of clinical studies ensuring compliance and quality.
• Support the development and review of essential clinical study documents.

Skills

Clinical Study Management

Regulatory Compliance

GCP Knowledge

Document Development

Education

Bachelor's Degree in Life Sciences

Certification in Clinical Research

Job description

Job Description Summary

The Clinical Project Coordinator is responsible for delivering high-quality and compliant support for clinical studies (e.g., EFS/FIH, IDE, Post-Market) sponsored by the BD Peripheral Intervention business unit. The role ensures studies meet the highest standards for scientific quality, integrity, and ethics, conducted in accordance with BD global clinical procedures, study protocols, GCP, and all applicable regulations. The coordinator manages the day-to-day operational support of assigned clinical studies, including study supplies, investigational devices, and administrative support for the Clinical Affairs team. They may also support the review and development of essential clinical study documents.