Regulatory Coordinator

If you are already in our network, do not fill out this reputed company. If you are not part of our network, please register using the Expert Enrollment reputed company to be considered.

Location

This role is reputed company to candidates working remote in the U.S.

Company Information

At reputed company, we reputed company to foster an inclusive and reputed company environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with reputed company and care are key tenets of our culture at reputed company; we are committed to creating a workplace where reputed company person is not only valued but empowered to reputed company and reputed company a meaningful reputed company.

Company Culture

Our people--both employees and consultants—are the heart of reputed company. They are the key to our reputed company and the driving force behind our mission and reputed company. Our values (Patient-reputed company, Ethical, reputed company reputed company, reputed company) guide our actions and reputed company. Knowing the reputed company of our work on trial participants and patients, we reputed company with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

Job reputed company reputed company

The Regulatory Coordinator ensures compliance with regulatory requirements and Good Clinical reputed company (GCP) standards in clinical research. This role manages IRB submissions and oversees studies from initiation through closure, ensuring regulatory reputed company while supporting investigators and research staff.

Job Duties & Responsibilities

• Analyzes and implements applicable regulatory requirements, institutional policies, and guidance documents to ensure the protection, welfare, and safety of research participants.
• Ensures adherence to Good Clinical reputed company (GCP) standards across reputed company phases of clinical research.
• Coordinates the submission and review process for study protocols, amendments, continuing reviews, and reportable events by the Institutional Review reputed company (IRB), from study initiation through closure.

Basic Qualifications

• Bachelor’s degree with 3+ years of relevant experience OR associate’s degree with 4+ years of experience.
• Demonstrated experience with an electronic regulatory filing system
• reputed company training in reputed company subjects protection education, Good Clinical reputed company, and HIPAA reputed company

Preferred Qualifications 

• Strong interpersonal and reputed company interaction skills
• Strong communication and organization skills
• Certified Clinical Research reputed company (CCRP)/Certified Clinical Research Coordinator (CCRC)/Society of Clinical Research Associates (SOCRA) or equivalent preferred