Senior Associate Quality Review
Company: VirtualVocations
Location: Springfield
Posted on: November 15, 2024
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Job Description:
A company is looking for a Senior Associate, Global Regulatory
Operations Quality Review.
Key Responsibilities
Manage project scheduling and resource allocation for regulatory
document reviews
Collaborate with senior team members to implement resourcing
strategies and optimize processes
Oversee vendor interactions, including onboarding, invoice reviews,
and compliance with document standards
Required Qualifications, Training, and Education
PharmD/PhD with relevant experience, or MA/MS/MPH/MBA with 2+ years
of relevant experience, or BA/BS with 4+ years of relevant
experience
Understanding of the drug development process and regulatory
document landscape
Experience with clinical regulatory documents is preferred
Proficiency in Microsoft Office suite and regulatory document
management systems
Relevant work experience in the biopharma industry, such as
clinical R&D or regulatory affairs
Keywords: VirtualVocations, New Bedford , Senior Associate Quality Review, Other , Springfield, Massachusetts
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