Regulatory Deliverables Coordinator

1 week ago


Canton, Michigan, United States MMS Full time
Regulatory Deliverables Coordinator Role
MMS is a leading CRO with a proven scientific approach to complex trial data and regulatory submission challenges. We're seeking an experienced Regulatory Deliverables Coordinator to provide operational support for clinical trial transparency, data sharing, and redaction of clinical trial documents.

Key Responsibilities
* Provide high-quality transparency deliverables in an efficient manner
* Ensure consistency and accuracy in document redaction or anonymization
* Maintain a strong understanding of regulations and guidance's as they pertain to transparency
* Lead projects with minimal management oversight

Requirements
* Bachelor's Degree in a scientific, medical, or clinical discipline or related field preferred; or 5 years of experience if less than a Bachelor's
* At least 3 years of previous transparency experience
* Hands-on experience with clinical trials and pharmaceutical development preferred

What We Offer
* Competitive salary: $130,000 - $160,000 per year
* Collaborative and inclusive work environment
* Opportunities for professional growth and development

How to Apply
Please submit your application if you're interested in this role.

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