Regulatory Affairs Associate

Overview: Monte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs. This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing and implementing regulatory strategies to support the...

Associate Director, Regulatory AffairsLocation: Boston, MA USAMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs. This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing...

Overview: **Responsibilities**: - The Associate Director of regulatory Affairs will be responsible for the development and execution of the Regulatory strategy for assigned programs in alignment with the corporate goals. - Lead and manage FDA and Health Authority interactions with FDA and global health authorities, including meetings, teleconferences, and...

Role: Regulatory Affairs Associate Location: Remote Duration: 7 Months Main Responsibilities Provide regulatory input to product lifecycle planning. Assist in SOP development and review. Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes. Understand and investigate regulatory history/background of...

Job Title: Director of Regulatory Affairs Job Description: As the Director of Regulatory Affairs in the medical device industry, you will play a pivotal role in ensuring that our products comply with all applicable regulatory requirements and standards. Leveraging your extensive knowledge of regulatory processes, you will lead the development and...

Job Title: Director of Regulatory AffairsJob Description:As the Director of Regulatory Affairs in the medical device industry, you will play a pivotal role in ensuring that our products comply with all applicable regulatory requirements and standards. Leveraging your extensive knowledge of regulatory processes, you will lead the development and...

Job Title: Director of Regulatory AffairsJob Description:As the Director of Regulatory Affairs in the medical device industry, you will play a pivotal role in ensuring that our products comply with all applicable regulatory requirements and standards. Leveraging your extensive knowledge of regulatory processes, you will lead the development and...

Job DescriptionJob DescriptionJob Title: Director of Regulatory AffairsJob Description:As the Director of Regulatory Affairs in the medical device industry, you will play a pivotal role in ensuring that our products comply with all applicable regulatory requirements and standards. Leveraging your extensive knowledge of regulatory processes, you will lead the...

Job Description Job Description Job Description We have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will interface with clients on different projects to provide consulting services. We are seeking entry-level experienced personnel or fresh graduate students...

Job DescriptionJob DescriptionJob DescriptionWe have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will interface with clients on different projects to provide consulting services.We are seeking entry-level experienced personnel or fresh graduate students willing...

Associate Director, Regulatory Affairs Advertising & Promotion page is loaded Associate Director, Regulatory Affairs Advertising & Promotion Apply locations Boston time type Full time posted on Posted 4 Days Ago job requisition id REQ-2604 The Associate Director, Regulatory Affairs Advertising & Promotion will be responsible for providing strategic,...

Responsibilities and Requirements: This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies. Be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. dditionally, this role leads the development of a global HA...

Location: REMOTESalary: $30.00 USD Hourly - $37.00 USD HourlyDescription: Our client is currently seeking a Regulatory Affairs Senior Associate Day to Day Responsibilities:Support the implementation of Veeva Vault, IDMP, EU CTR, and other regulatory initiatives.Work with stakeholders to gather requirements and develop solutions.Provide Subject Matter...

Associate Director/Director, Regulatory Affairs, CMC Boston, MA, USA Req #249 Monday, April 1, 2024 Who We Are: Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE ) is a neuroscience-focused biopharmaceutical company committed to discovering, developing, and commercializing innovative therapeutics to improve the lives of people living with neurological and...

Our client is a clinical stage biopharmaceutical company. They have asked us to assist them in their search for a Director, Regulatory Affairs. Major tasks and responsibilities include:Supports global regulatory strategy and execution on development programs, including maintaining strong relationships with cross-functional internal colleagues, regulatory...

Senior Manager/Associate Director, Regulatory Strategy Company Overview: Inozyme Pharma, Inc. (Nasdaq: INZY) is a clinical-stage rare disease biopharmaceutical company developing novel therapeutics for the treatment of diseases of abnormal mineralization impacting the vasculature, soft tissue, and skeleton. Through our in-depth understanding of the...

Senior Manager/Associate Director, Regulatory Strategy Company Overview: Inozyme Pharma, Inc. (Nasdaq: INZY) is a clinical-stage rare disease biopharmaceutical company developing novel therapeutics for the treatment of diseases of abnormal mineralization impacting the vasculature, soft tissue, and skeleton. Through our in-depth understanding of the...

Job Description Job Description BrioHealth Solutions Inc., Inc. is seeking a skilled and self-motivated Principal Regulatory Affairs Specialist to join our growing team. As a principal regulatory affairs specialist at BrioHealth Solutions Inc., you’ll support product development activities for Class III Medical Devices and have responsibility for preparing...

Senior Manager/Associate Director, Regulatory StrategyCompany Overview:Inozyme Pharma, Inc. (Nasdaq: INZY) is a clinical-stage rare disease biopharmaceutical company developing novel therapeutics for the treatment of diseases of abnormal mineralization impacting the vasculature, soft tissue, and skeleton. Through our in-depth understanding of the biological...

Job DescriptionJob DescriptionBrioHealth Solutions Inc., Inc. is seeking a skilled and self-motivated Principal Regulatory Affairs Specialist to join our growing team. As a principal regulatory affairs specialist at BrioHealth Solutions Inc., you’ll support product development activities for Class III Medical Devices and have responsibility for preparing...