Paralegal Specialist for Regulatory Affairs

3 weeks ago


Boston, Massachusetts, United States Dexian DISYS Full time

Job Title: Paralegal Specialist for Regulatory Affairs

Job Summary:

We are seeking a skilled Paralegal Specialist to join our team at Dexian DISYS. As a Paralegal Specialist for Regulatory Affairs, you will be responsible for providing administrative support to our regulatory team.

Key Responsibilities:

  • Complete data entry onto excel spreadsheets, sort data, and perform analytics as requested.
  • Draft letters to be sent to licensees, including dismissal letters.
  • Transfer cases to prosecution, tracking any additional information as necessary.
  • Electronically scan letters and other applicable documents, and summarize them into electronic folders.
  • Work with large databases, maintaining both electronic and manual files.
  • Answer emails and provide minimal direction.

Requirements:

  • Paralegal level of knowledge is essential.
  • Bachelors degree required.
  • Paralegal experience and or certification required.

About Dexian DISYS:

Dexian DISYS is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. We are committed to providing our clients with the best talent and technology to achieve their goals.



  • Boston, Massachusetts, United States Katalyst Healthcares and Life Sciences Full time

    Job Title: Regulatory Affairs SpecialistAt Katalyst Healthcares and Life Sciences, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will play a critical role in ensuring the compliance of our medical devices with global regulatory requirements.Responsibilities:Develop and implement...


  • Boston, Massachusetts, United States Katalyst Healthcares and Life Sciences Full time

    Job SummaryAs a Regulatory Affairs Specialist at Katalyst Healthcares and Life Sciences, you will play a critical role in ensuring the compliance of our medical devices with global regulatory requirements. You will develop and implement global regulatory strategies for new and modified medical devices, providing regulatory guidance to cross-functional...


  • Boston, Massachusetts, United States Foundation Medicine Full time

    Job DescriptionThe Senior Specialist, Regulatory Affairs plays a pivotal role in supporting the regulatory submissions process by developing strategic plans and submitting materials to health authorities such as the FDA for approval of novel platforms.This position provides critical regulatory guidance to internal development teams and prepares comprehensive...


  • Boston, Massachusetts, United States Foundation Medicine Full time

    Job SummaryThe Senior Specialist, Regulatory Affairs will play a key role in supporting the regulatory submissions process through the development of regulatory strategy and submission of materials to health authorities such as the FDA for approval of novel platforms. This position will provide regulatory guidance to internal development teams and prepare...


  • Boston, Massachusetts, United States PathAI Full time

    Regulatory Affairs Specialist RolePathAI is seeking an experienced Regulatory Affairs Specialist to support the development and approval of our diagnostic products. As a key member of our regulatory team, you will work closely with cross-functional teams to ensure compliance with regulatory requirements and guidelines.Key Responsibilities:Prepare and manage...


  • Boston, Massachusetts, United States Foundation Medicine Full time

    About the RoleThe Senior Specialist, Regulatory Affairs plays a critical role in supporting the regulatory submissions process by developing regulatory strategies and submitting materials to health authorities such as the FDA for approval of novel platforms. This position provides regulatory guidance to internal development teams and prepares document...


  • Boston, Massachusetts, United States WHITE COLLAR TECHNOLOGIES INC Full time

    Job OverviewWhite Collar Technologies Inc. is seeking a highly skilled Regulatory Affairs Associate to join our team. As a key member of our life science consulting team, you will be responsible for ensuring compliance with regulatory requirements and providing expert guidance to clients.Key Responsibilities:Develop and implement regulatory strategies to...


  • Boston, Massachusetts, United States ProClinical Full time

    Senior Director, Regulatory Affairs **Job Summary:** Proclinical is seeking a dynamic and strategic leader for the role of Senior Director of Regulatory Affairs. This position is pivotal in driving regulatory efforts for vaccine development programs. **Primary Responsibilities:** * Manage the full lifecycle of global regulatory submissions and approvals,...


  • Boston, Massachusetts, United States PathAI Full time

    Join Our Team at PathAIPathAI is a pioneering company in the field of AI-powered pathology, dedicated to improving patient outcomes. We are seeking an experienced Principal Regulatory Affairs Specialist to play a key role in supporting our regulatory strategies and ensuring the success of our diagnostic products in the global market.This role involves...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics Full time

    Regulatory Affairs ProfessionalMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to support the global development and approval of our innovative therapies.This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing and implementing...


  • Boston, Massachusetts, United States Takeda Pharmaceutical Full time

    About the Role:Takeda Pharmaceutical is seeking a highly skilled Regulatory Affairs Manager to support the execution of regulatory CMC investigational, registration, and post-approval tasks for assigned products. As a key member of the Regulatory Affairs CMC team, you will work closely with cross-functional teams to develop project plans for global...


  • Boston, Massachusetts, United States Fairway Consulting Group Full time

    Job Summary:Fairway Consulting Group is seeking a highly experienced Regulatory Affairs Director to lead our client's global regulatory strategy and execution on development programs. The ideal candidate will have a comprehensive knowledge of the drug development process, global regulations and guidelines, and a comprehensive understanding of global...


  • Boston, Massachusetts, United States Cambridge Associates Full time

    Job Opportunity at Cambridge AssociatesWe are seeking an experienced Corporate Paralegal to join our global Legal and Compliance department. The successful candidate will be responsible for reviewing and negotiating NDAs and vendor agreements, drafting, reviewing, and announcing various contractual matters, including client contracts and amendments.Key...


  • Boston, Massachusetts, United States Monte Rosa Therapeutics Full time

    Regulatory Affairs Senior Manager**Job Summary:**Monte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team. This role will focus on oncology, immunology, and related therapeutic areas.**Key Responsibilities:*** Develop and implement regulatory strategies to support the global development and approval of...


  • Boston, Massachusetts, United States Takeda Pharmaceutical Full time

    About the Role:Takeda is a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients worldwide. We are seeking a highly skilled Manager, Global Regulatory Affairs CMC Submission Management to support the execution of regulatory CMC investigational, registration and post-approval tasks for assigned...

  • Paralegal Coordinator

    3 weeks ago


    Boston, Massachusetts, United States CMBG3 Law, LLC Full time

    Job DescriptionCMBG3 Law, LLC is a certified majority women-owned law firm with a diverse team of attorneys, litigators, lobbyists, consultants, paralegals, and staff. Our proactive approach to solving legal problems involves best-in-class business counsel, regulatory compliance, risk prevention, government affairs advocacy, litigation, and national...

  • Paralegal Specialist

    3 weeks ago


    Boston, Massachusetts, United States BCforward Full time

    Job Title: Paralegal SpecialistJob Summary:BCforward is seeking a highly motivated Paralegal Specialist to join our team. The successful candidate will work with two complaint resolution coordinators on processing completed discipline determinations on licensed nurses. Must be a certified Paralegal.Key Responsibilities: Process completed discipline...


  • Boston, Massachusetts, United States Xenon Inc Full time

    About the RoleWe are seeking a highly skilled Senior Manager, Regulatory Affairs to join our team at Xenon Inc. This role will be responsible for developing and implementing global regulatory strategies to support the advancement of our product pipeline.ResponsibilitiesProvide regulatory support on multidisciplinary project/clinical study teams, including...

  • Paralegal Specialist

    3 weeks ago


    Boston, Massachusetts, United States Trove Brands Full time

    Job Title: Paralegal SpecialistAbout the Role:Trove Brands is seeking a skilled Paralegal Specialist to support our legal team in Overland Park, KS. As a key member of our team, you will play a vital role in enhancing attorneys' effectiveness by developing case information, evidence, and settlement options, tracking cases, and supporting attorneys' hearing...


  • Boston, Massachusetts, United States Cambridge Associates Full time

    Our global Legal and Compliance department is seeking an experienced corporate paralegal to join our collegial and collaborative team environment. As a key member of our team, you will be responsible for reviewing and negotiating agreements with vendors, drafting, reviewing, and internally announcing various contractual matters, including client contracts...