English Associate

4 weeks ago

New Haven CT, United States Precision Life Sciences Full time

Associate Director/Director, Regulatory Affairs Submissions and Operations
This role reports to the Senior Director of Global Regulatory Affairs with the primary objective to execute and pull through regulatory strategy and guidance, ensuring a fully compliant and successful outcome for the company and partners. The selected candidate must have a working knowledge of global regulations, submission practices and requirements with proven attentiveness to detail to translate the company regulatory strategy into compliant submissions and best practices.
Regulatory submission planning, prioritization, execution and successful delivery to health authorities.
Various Operational aspects of regulatory submissions including document management.
Support for Regulatory Strategy including providing input on the regulatory development plan.
The incumbent will work in a close cross-functional partnership with all functions within the company. as well as with Contract Research Organizations, alliance partners and vendors performing work on behalf of the company.
Regulatory Operations
Serves as a subject matter expert on US and global regulatory matters (i.e. global regulations, current guidance and changes, electronic submissions and platforms)
Identifies compliance issues to Regulatory management to facilitate remediation and continuous improvement with the appropriate stakeholders
Maintains awareness of Regulatory Health Authority Policy, trends, and changes that could impact the submission space (ICH, electronic requirements, submission content.)
Provides oversight and guidance for regulatory documents and dossiers in accordance with company policies and SOPs
Implements and organizes/manages an Electronic Document Management platform to establish taxonomy, naming conventions, version control and audit trail maintenance including monitoring 21CFR Part 11 Compliance
Provides regulatory operational documentation support for submission components to ensure documents comply with electronic guidance
Ensure all regulatory authors have training and access to the appropriate authoring templates and shared drive(s) Regulatory Submission Management
Provides oversight on routine regulatory submissions, such as those for IND safety reports, clinical site documentation updates (1572s), lot releases, promotional pieces and protocol amendments
Provides regulatory project management for submission deliverables such as INDs and IND amendments, CTAs and amendments, NDAs, BLAs and amendments/supplements, MAAs and Variations in accordance with applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc).
Provides guidance to development team to ensure that company timelines embed requirements that are dictated by regulatory guidance
Facilitates cross functional regulatory teams (internal staff and external CROs and partners) to develop regulatory submission content plans and execute them. Leads and guides participants in critical thinking along with decision-making criteria to ensure content quality optimization and speed towards submissions.
Provides regulatory review of draft documentation and submissions (including for potential to outsource activities to third party companies (under special agreement arrangements)
Submits new INDs including potential administrative splits for FDA Divisions to facilitate development plans
Drafts and submits submissions such as orphan drug, breakthrough therapy and fast track applications
Coordinates and manages marketing application (NDA, BLA, MAA) planning and submission
Improves operational effectiveness to increase the efficiency of procedures, processes and systems while increasing awareness of standards and compliance with regulations and law
Supports the regulatory aspects of partnerships in foreign countries
Acts as the point of contact for CROs and partners to provide documents/dossiers and communicate on regulatory questions Other responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
BS, MS or PhD in a scientific field
~10-15 years of Regulatory Experience
~ Global Regulatory Submission Management experience including INDs, NDAs, CTAs
~ Familiarity with ICH and Global Health Authority regulation and guidance which governs investigational drug development and marketing applications
~ Experience reviewing and writing Standard Operating Procedures Competencies:
~ Able to read, comprehend, write, and speak English fluently
~ Able to communicate complex information clearly and succinctly, both in writing and orally
~ Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook), SharePoint, Box, Adobe Pro
~ Ability to multi-task, manage and prioritize various and differing projects, as well as work effectively toward numerous deadlines

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