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Associate Manager, Regulatory Operations (Remote)

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Legal & ComplianceRegulatory
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Quick Summary

Overview

function googleTranslateElementInit() { new google.translate.TranslateElement({pageLanguage: 'en'}, 'google_translate_element'); } Associate Manager, Regulatory Operations (Remote)…

Key Responsibilities

Collaborate with cross-functional teams to develop and execute regulatory strategies and submission plans, focusing on regulatory filings for Rest of World (RoW) regions.

Requirements Summary

Bachelor’s or higher degree in a related field with at least 4 years of experience in the biopharmaceutical industry, preferably in regulatory project management or a related discipline. PMP or similar project management certification is preferred.

Technical Tools
ms-officeproject-management

CEDENT

Summary

We are looking for an Associate Manager, Regulatory Project Manager to provide regulatory project management support across a growing portfolio. This role is part of the Global Regulatory Project Management function and supports regulatory submissions including NDAs, BLAs, INDs, CTAs, and other regional filings. The ideal candidate will coordinate regulatory strategies, timelines, and deliverables while ensuring alignment with corporate goals.
 

Responsibilities
  • Collaborate with cross-functional teams to develop and execute regulatory strategies and submission plans, focusing on regulatory filings for Rest of World (RoW) regions.

  • Create and manage high-level and detailed regulatory timelines using project management software, ensuring alignment with corporate objectives.

  • Facilitate regulatory team and working group meetings, including scheduling, preparing agendas, distributing documentation, and ensuring action item follow-up.

  • Coordinate and track regulatory documents for submissions, ensuring compliance with ICH guidelines, regional requirements, and company policies.

  • Maintain transparent and timely communication about submission-related activities, keeping all stakeholders informed of progress and status.

  • Proactively identify and address potential issues that could impact project timelines or deliverables.

  • Support the development and continuous improvement of regulatory business processes, tools, templates, dashboards, and project management practices.
     

Requirements
  • Bachelor’s or higher degree in a related field with at least 4 years of experience in the biopharmaceutical industry, preferably in regulatory project management or a related discipline.

  • PMP or similar project management certification is preferred.

  • Working knowledge of drug development processes and regulatory agency regulations, guidelines, and submissions.

  • Proficiency in project management tools such as Microsoft Project and Smartsheet, as well as the MS Office suite.

  • Demonstrated ability to manage multiple tasks, prioritize effectively, and meet deadlines.

  • Strong verbal and written communication skills, attention to detail, and the ability to collaborate effectively in a team environment.

  • Self-motivated and capable of working independently within a matrix organization.

    Compensation 
    Hourly Rate Range - $45-$60/ hr 

    Benefits Offered:
    [Health, Dental, Vision Insurance]

    Deadline: Applications accepted until 04/30/2026 at 11:59 PM CST

    We are an Equal Pay Employer. All employment decisions, including compensation, benefits, hiring, training, and promotions, are made based on merit, qualifications, and business needs. We do not discriminate on the basis of gender, race, ethnicity, age, disability, sexual orientation, or any other protected characteristic. We are committed to ensuring equal pay for equal work and regularly review our compensation practices to promote fairness, equity, and transparency across our organization.

     

     

Department: Direct Clients
This is a full time position

Visit Careers at CEDENT

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Location & Eligibility

Where is the job
Location terms not specified

Listing Details

First seen
May 6, 2026
Last seen
May 8, 2026

Posting Health

Days active
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Trust Level
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Scored at
May 6, 2026

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dtAssociate Manager, Regulatory Operations (Remote)