Director of Regulatory Affairs

6 month contract with potential to extendFlorham, NJ- hybrid 2x a week onsiteSupport the Global Therapeutic Area Lead (GTAL), Regulatory Affairs (Senior Director) in developing and executing regulatory strategies for antimicrobial antifungal programs globally or within specific regions Specific tasks:Assisting in preparing presentations, reports, and strategic documents for leadership discussions.Maintaining and tracking project timelines, action items, and regulatory deliverables to ensure smooth anizing and documenting meeting minutes and action items to support the leader's strategic planning.Contribute to the preparation and submission of regulatory documents related to antimicrobial antifungal programs to regulatory authorities.Conducting research on regulatory trends, competitor strategies, and market intelligence to provide background insights. Assist in Coordinating with Global Regulatory Counterparts to Align Regional Strategies and Submissions with Global Development Plans and Regulatory Strategy Plans:Specific Tasks:Maintaining centralized regulatory meeting minutes to track planning and progress of key submissions, including timelines, status updates, and regulatory requirements across regions.Scheduling and organizing cross-functional and cross-regional meetings, preparing agendas, and summarizing discussions. Assist in Managing Regulatory Risks and Developing Mitigation Strategies for Anti-Infective Initiatives:Specific Tasks:Maintaining a regulatory risk log, tracking identified risks, mitigation plans, and follow-up actions.Conducting literature reviews and research on regulatory guidelines to provide preliminary insights.Drafting initial risk assessment summaries for leadership to review and refine. Provide Regulatory Guidance and Support for Post-Marketing Activities Related to Marketed Anti-Infectives: Specific Tasks:Assisting in preparing draft regulatory documents under the guidance of senior regulatory staff.Tracking post-marketing requirements and submission deadlines to ensure compliance.Conducting basic document reviews for formatting, consistency, and completeness before piling and organizing historical regulatory data for reference and audits. Assist in Preparing Regulatory Updates, Progress Reports, and Strategic Recommendations for Senior Leadership:Specific Tasks:Gathering regulatory intelligence and compiling data for leadership reports.Assisting in drafting initial versions of regulatory updates, subject to review and refinement.Creating visual summaries, presentations, and dashboards to convey regulatory insights effectively.Maintaining a library of past regulatory updates for reference and consistency. Establish Deliverables and Performance Expectations:Specific projects to be completed include:preparation of Type CBD Meetings for antimicrobials in clinical development (as needed)contributions to finalization of regulatory strategy plans for antimicrobials in developmentpreparation of sNDA for marketed antimicrobialKnowledge of and Compliance with FDA, EMEA, PMDA guidancesPerformance will be monitored via regularly review by the GTAL and feedback on the strategist's work. This will include review of meeting minutes, timelines and draft submission packages. Performance metrics will include completion of regulatory submissions, adherence to timelines, and the quality of submissionsThe GTAL Regulatory Affairs will review and approve completed work. Minimum Qualifications:Bachelor's degree in a scientific discipline such as life sciences, pharmacy, bioscience; advanced degree preferred.10+ years of experience in regulatory affairs within the pharmaceutical or biotech industryDemonstrated ability to work effectively in a cross-functional team environment.Strong knowledge of regional regulatory requirements and guidelines, including FDA regulations and ICH guidelines.Excellent communication and interpersonal skills.pay within this range will be commensurate with level of experience

Created: 2025-03-07