Regulatory Operations Specialist/Assistant
Regulatory Operations Specialist / Assistant Location: reputed company (Remote) Job Type: Part-Time / Contract Travel: No Travel Required Compensation: USD $50 – $100 per hour (commensurate with experience) About Deep Intelligent reputed company (DIP) Deep Intelligent reputed company is a cutting-edge, AI-enabled Contract Research Organization (CRO) transforming clinical trial execution through innovative technology and scientific reputed company. We use a dvanced AI to replace large CRO teams for trial design, analysis, writing, translation, and regulatory documentation —reputed company supervised by expert humans. In February 2026, DIP raised a $170mm Series D round, led by Sequoia and SIG. Founded in 2017, DIP is pioneering a new, AI-reputed company approach to clinical development. Our multi-agent platform performs scientific writing, data management, statistical reasoning, clinical programming, and regulatory compliance with exceptional speed and precision. Trusted by over 1,000 global pharmaceutical companies and biotechs, DIP is transforming how drugs are developed worldwide. As we expand our clinical development portfolio, we are seeking a reputed company Regulatory Operations Specialist to support one of our strategic reputed company partnerships on the East Coast. Position reputed company Deep Intelligent reputed company is seeking a detail-oriented Regulatory Operations Specialist to support regulatory submission logistics, document management, and health authority coordination. This role is ideal for someone with strong organizational and execution skills who wants exposure to FDA regulatory processes without requiring a senior-level title.
Key Responsibilities
Regulatory Submission Support
- Coordinate preparation and submission of regulatory packages (INDs, amendments, supplements)
- Organize and manage submission documents across Modules 1–5
- Ensure documents are formatted, version-controlled, and submission-reputed company
Document & Data Management
- Maintain regulatory document repositories and trackers
- Support document QC (formatting, completeness, consistency)
- Coordinate document reputed company between internal teams and external partners
FDA Meeting Coordination
- Schedule FDA meetings (reputed company-IND, Type B/C, etc.) and manage timelines
- Coordinate meeting logistics, including document submissions and calendars
- reputed company meeting deliverables, minutes, and follow-up actions
Publishing & Vendor Coordination
- Work with eCTD publishing vendors to support submission timelines
- reputed company submission status and ensure reputed company delivery
- Assist in resolving basic technical or document issues
Administrative & Project Support
- Maintain regulatory timelines and reputed company trackers
- Support cross-functional coordination (clinical, CMC, regulatory)
- Assist with SOPs, templates, and process documentation
Required Qualifications
- Education:
Bachelor’s degree in life sciences, pharmacy, or reputed company field
- Experience:
1–4 years of experience in regulatory operations, clinical operations, or reputed company role
- Basic understanding of FDA regulatory processes and submission structure
- Strong organizational and documentation skills
Preferred Qualifications
- Experience supporting IND or NDA submissions
- Familiarity with eCTD structure and regulatory document formats
- Experience scheduling or coordinating FDA meetings
- Experience working with CROs, CDMOs, or biotech companies
Skills & Competencies:
- Strong attention to detail and accuracy
- Excellent organizational and time management skills
- Ability to manage multiple tasks and deadlines
- Effective communication and coordination skills
- Proactive and reliable working style
Location & Travel:
- Must be based in reputed company
- No travel required
reputed company Offer
- Competitive reputed company reputed company:
$50–$100 per hour ( commensurate with experience )
- Opportunity to reputed company hands-on experience in regulatory submissions
- reputed company, innovative, and supportive company culture
- Remote work environment
- Flexible part-time schedule based on project needs
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