Senior Regulatory Operations Specialist

2 months ago


Princeton, United States MRMMcCann Full time

Job Title: Senior Regulatory Operations Specialist

About this role:

The Senior Regulatory Operations Specialist position is an integral part of MRM for Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and Regulatory (MLR) groups.

This position will support the Princeton pharmaceutical/health Client base. The Senior Regulatory Operations Specialist will manage submission workflow and capacity for specific brands and work to achieve expert level status on Client regulatory submission, collaboration, and archive platforms/tools. This includes a supporting role in adhering to and maintaining processes and requirements for the capability.

Responsibilities:

  • Serve as day-to-day submissions lead; manage and filter workload to team members
  • Demonstrate general knowledge of Regulatory Affairs and guidelines that govern advertising and promotional material according to FDA
  • Work cross functionally with Project Management to ensure submission timelines are met and all material is gathered for accurate and timely submissions
  • Learn client-based submission systems and be able to navigate for efficient use, including the tagging and linking of references based on annotations provided by Copy team
  • Maintain reference library and asset library for internal cross-functional use
  • Execute submissions in the following manner:
    • Initiate the submission process
    • Track the project from kickoff through to final submission Client MLR approval
    • Organize submission materials in accordance with the Client dictated requirements
    • Ensure integrity of submission materials to ensure adherence with Client MLR requirements
    • Submit materials via Client MLR submission platform/tool
    • Provide status updates on submission progresses
    • Support team with prepping and sending final samples, and 2253 materials when needed
  • Record keeping and knowledge base:
    • Document and maintain project tracker
    • Document and maintain current Client requirements for MLR submission
    • Maintain knowledge of the Client MLR schedule
    • Utilize and maintain regulatory document control and appropriate distribution of regulatory documents

  • Requirements:
  • 4+ years of experience in a relatable role preferred
  • Familiarity with agency submission process and MLR preferred
  • Must have strong interpersonal and problem-solving skills; be able to build strong relationships within the agency and client organizations, and must be able to participate in client and internal agency meetings with senior personnel
  • Must be able to manage multiple projects as one cohesive program
    • Capacity for risk identification and management
    • Strong sense of ownership of process and results
  • Strong writing and verbal skills
  • Highly organized and detail oriented with an ability to influence others in these areas
  • Ability to find creative solutions to complex problems and multi-task
  • Must be comfortable working in an environment that utilizes electronic docbases, databases, and computer systems (Microsoft Office, Veeva Vault, Zinc, and web based applications)
  • MS Office experience and competence required
  • Workload management and people supervisory experience a plus

About MRM

MRM is a modern relationship marketing agency that delivers transformative creative solutions at the intersection of business, culture, and technology. MRM operates in a borderless, integrated way, to allow for greater collaboration and velocity-all to the service of helping businesses grow meaningful relationships with people. MRM is part of McCann Worldgroup and the Interpublic Group of companies (NYSE: IPG), and spans 35 offices across North America, Latin America, Europe, the Middle East, and Asia Pacific. For more information, please visit www.mrm.com.

We love our diverse workplace MRM is an equal opportunity employer and does not discriminate on the basis of race, color, gender, religion, age, sexual orientation, national or ethnic origin, disability, marital status, veteran status or any other occupationally irrelevant criteria.



  • Princeton, United States MRMMcCann Full time

    Job Title: Senior Regulatory Operations Specialist About this role: The Senior Regulatory Operations Specialist position is an integral part of MRM for Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and Regulatory...


  • Princeton, New Jersey, United States MRINetwork Jobs Full time

    Position OverviewA dynamic company within the Pharmaceutical sector is seeking a Senior Regulatory Compliance Specialist.This position entails the preparation and evaluation of various regulatory submissions to relevant authorities. The Specialist will work in close collaboration with senior leadership in Regulatory Affairs, concentrating on activities such...


  • Princeton, New Jersey, United States MRMMcCann Full time

    Senior Regulatory Operations SpecialistOverview:The Senior Regulatory Operations Specialist plays a crucial role in the preparation, assessment, and submission of regulatory documentation to the Client Medical, Legal, and Regulatory (MLR) teams. This position is essential for supporting the pharmaceutical and healthcare sectors within the Princeton client...


  • Princeton, United States Intellectt Inc Full time

    Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12 MonthsYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsSkills:Have working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave experience...


  • Princeton, United States Intellectt Inc Full time

    Role: Senior Regulatory Affairs Specialist Location: Princeton, NJ 08540 Duration: 12 MonthsKey Responsibilities:Collaborate with multiple business units to develop, update, and enhance regulatory affairs processes.Assist in strategy implementation and operations for regulatory affairs, including product registration submissions, progress reports, and...


  • Princeton, United States Intellectt Inc Full time

    Role: Senior Regulatory Affairs Specialist Location: Princeton, NJ 08540 Duration: 12 MonthsKey Responsibilities:Collaborate with multiple business units to develop, update, and enhance regulatory affairs processes.Assist in strategy implementation and operations for regulatory affairs, including product registration submissions, progress reports, and...


  • Princeton, United States Experis Full time

    Experis IT ManpowerGroup has partnered with a leading Medical device organization in the Princeton , NJ for a Senior Regulatory Affairs Specialist role to assist their team. This is an on-site role. Industry: Medical device Title: Senior Regulatory Affairs Specialist Pay Rate:$80-100/hr on W2 Location: Princeton, NJ ( Onsite 100% ) Duration:12...


  • Princeton, United States Intellectt Inc Full time

    Job Details:Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12 MonthsYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsSkills:Have working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave...


  • Princeton, United States Intellectt Inc Full time

    Job Details:Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12 MonthsYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsSkills:Have working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave...


  • Princeton, United States Intellectt Inc Full time

    Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJDuration: 12 MonthsJob Description: Years’ Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsResponsibilities: This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy...


  • Princeton, United States Experis Full time

    Experis IT ManpowerGroup has partnered with a leading Medical device organization in the Princeton, NJ for a Senior Regulatory Affairs Specialist role to assist their team. This is an on-site role.    Industry:         Medical device Title:                 Senior Regulatory Affairs Specialist Pay Rate:        $80-100/hr on...


  • Princeton, United States Intellectt Inc Full time

    Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12+ MonthsCore job responsibilities for this role may include:This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy implementation and operations for regulatory affairs activities, including...


  • Princeton, United States Select Source International Full time

    Job DescriptionJob DescriptionJob Title: Senior Regulatory Affairs SpecialistLocation: - Princeton, NJ 08540Duration: - 12 Month contract with possible extension based on performanceAs an individual contributor, the function of a Senior Regulatory Affairs Specialist is to combine knowledge of scientific, regulatory, and business issues to enable i-STAT...


  • Princeton, United States Collabera Full time

    Job DescriptionJob DescriptionPrimary Job Function:·         As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to combine knowledge of scientific, regulatory, and business issues to enable branded products that are developed, manufactured, or distributed to meet required legislation in the US and...


  • Princeton, United States KYYBA Full time

    Job DescriptionJob DescriptionSenior Regulatory Affairs SpecialistPrinceton, NJ12+ month’s contractIVD Devices EXP in Regulatory AffairsExp with US 510K Submission in the last 5 yearsWriting submissions with Cross Functional TeamsExcellent Technical Writing SkillsGood Communication skillsOnsite 100%Technical Writing Examples would be preferred.MINIMUM...


  • Princeton, United States Select Source International Full time

    Job DescriptionJob DescriptionJob Title:  Regulatory Specialist IILocation:   Princeton NJ 08540Duration: 12 Months  CORE JOB RESPONSIBILITIES:Responsible for compiling and maintaining US 510k submission and EU IVDR Technical File.Responsible for compliance with applicable Corporate and Divisional Policies and procedures under the quality system. Core...


  • Princeton, New Jersey, United States Intellectt Inc Full time

    Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncRole Overview: The Senior Regulatory Affairs Specialist will play a pivotal role in ensuring compliance with regulatory standards and enhancing operational processes within the organization.Key Responsibilities:Engage with various departments to refine and advance regulatory affairs...


  • Princeton, New Jersey, United States Intellectt Inc Full time

    Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncRole Overview: The Senior Regulatory Affairs Specialist will play a crucial role in overseeing and enhancing regulatory processes within the organization.Key Responsibilities:Engage with various departments to refine and improve regulatory affairs methodologies.Support the execution of...


  • Princeton, United States KYYBA Full time

    Job DescriptionJob DescriptionYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsHave working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave experience supporting internal and external inspectionsWork cross-functionally and in...


  • Princeton, New Jersey, United States Intellectt Inc Full time

    Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncRole Overview:This role involves collaborating with various departments to enhance and refine regulatory affairs processes. The specialist will support the execution of strategies and operations related to regulatory affairs, which includes overseeing the preparation of product registration...