Overview
The contractor will support the Promotional Review Committee (PRC) process by coordinating submission logistics, ensuring compliance with internal processes, and facilitating cross-functional collaboration across marketing, regulatory, medical, legal, and creative teams.
- Reporting to: Director, Creative
- Location: Fully Remote
- Employment Type: Contract, $40/.00/hr
Required Qualifications & Experience
The contractor should possess the following qualifications:
- Familiarity with the MLR (Medical, Legal, Regulatory) review process within aesthetics, pharmaceutical, biotech, or other FDA-regulated life sciences environments
- Experience working with Veeva Vault or similar promotional review/content management systems
- Demonstrated ability to review materials for accuracy, completeness, and compliance prior to submission
- Experience collaborating cross-functionally with marketing, regulatory, medical, legal, and creative stakeholders
- Background in traffic coordination or project management within an agency, marketing, or commercial team
- Minimum of 2-3 years of professional experience in a corporate environment
- Proficiency in Microsoft Office applications
Core Competencies (Soft Skills)
- Strong organizational skills with exceptional attention to detail
- High level of accountability and accuracy in reviewing and tracking submission materials
- Ability to manage multiple deadlines with strong time management skills
- Process-oriented mindset with the ability to adapt to changing priorities
- Proactive, self-motivated, and reliable
- Clear and professional communication skills across cross-functional teams
Scope of Work / Responsibilities
The contractor will be responsible for:
- Coordinating PRC submission logistics and managing timelines to ensure materials are submitted and reviewed on schedule
- Maintaining dashboards to track current, upcoming, and completed submissions, including review stages, job codes, and deadlines
- Managing submission materials within Veeva Vault, ensuring all required components are complete prior to review
- Performing quality control checks to ensure accuracy, completeness, and adherence to PRC requirements
- Documenting reviewer feedback, requested revisions, and next steps, and communicating updates to stakeholders
- Collaborating with cross-functional teams, including PR, Regulatory, Medical, Legal, Marketing, Operations, and Creative Studio, to route materials through the review process
- Providing operational support during periods of high submission volume
- Assisting with preparation for PRC review meetings as needed
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