Regulatory Affairs Manager

Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

Immediate Need for a Manager, Regulatory Affairs with a biotech company in Florham Park, NJ. Hybrid position with 2 days in office in Florham Park. 1 year renewable contract.Must have strong regulatory strategy experience.OverviewThe Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior...

Insight Global is seeking a Sr. Manager of Regulatory Affairs to join one of our pharmaceutical clients in Florham Park, NJ. This position is responsible for assisting with the development and execution of regional regulatory strategies for its therapeutics division. It is essential that this person has experience working with therapeutics and possesses a...

Insight Global is seeking a Sr. Manager of Regulatory Affairs to join one of our pharmaceutical clients in Florham Park, NJ. This position is responsible for assisting with the development and execution of regional regulatory strategies for its therapeutics division. It is essential that this person has experience working with therapeutics and possesses a...

Insight Global is seeking a Sr. Manager of Regulatory Affairs to join one of our pharmaceutical clients in Florham Park, NJ. This position is responsible for assisting with the development and execution of regional regulatory strategies for its therapeutics division. It is essential that this person has experience working with therapeutics and possesses a...

Florham Park, NJ- onsite 2-3x a week1 year contract with potential to extendOverview:The Associate Director, Regulatory Affairs – GDP Contractor, provides essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves assisting in the development and...

Florham Park, NJ- onsite 2-3x a week1 year contract with potential to extendOverview:The Associate Director, Regulatory Affairs – GDP Contractor, provides essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves assisting in the development and...

Responsibilities: Manages most aspects of company regulatory interface with domestic and international health authorities. Manages the development and deployment of the regulatory program that ensures aggressive product approval. Manages and may generate regulatory submission documents for new products or changes to existing health authorities' filings,...

Key Responsibilities:As a Regulatory Affairs Specialist at Katalyst Healthcares & Life Sciences, you will be responsible for managing the company's regulatory interface with domestic and international health authorities. This includes developing and deploying the regulatory program to ensure aggressive product approval. You will also manage and generate...

Job Title: Sr. Regulatory Affairs SpecialistJoin iHealth Labs Inc, a leading provider of cloud-connected medical devices, personal health care devices, and home-based tests, as a Sr. Regulatory Affairs Specialist. In this role, you will be part of the regulatory team responsible for proper oversight of medical device development and market introduction.Key...

Overview The Associate Director/Director, Regulatory Affairs - Global Development Products (Anti-Viral), provides essential support to the Executive Director in overseeing regulatory activities related to antiviral initiatives on a regional and/or global scale. This role involves assisting in the development and execution of regulatory strategies, regulatory...

Job SummaryAbbVie is seeking a highly skilled Medical Director, Medical Affairs to provide strategic and operational input into core medical affairs activities. The ideal candidate will have a strong understanding of relevant therapeutic areas and experience in generating clinical and scientific data.Key Responsibilities:Contribute to the development of...

Purpose As our Senior Manager of Rates and Regulatory Affairs you will collaborate with the Transformation and Regulatory Teams, contributing to the success of rate case filings across multiple states and commodities. Reporting to the Senior Director, Rates & Regulatory Affairs, you will be instrumental in preparing regulatory materials and supporting...

Job SummaryAs a Senior Manager of Rates and Regulatory Affairs at Liberty Utilities, you will play a critical role in collaborating with the Transformation and Regulatory Teams to drive the success of rate case filings across multiple states and commodities. Reporting to the Senior Director, Rates & Regulatory Affairs, you will be responsible for preparing...

Job Title: Scientific Director, Medical Affairs- CNS/PsychiatryJob Summary:We are seeking a highly skilled Scientific Director to join our Medical Affairs team in CNS/Psychiatry. As a key member of our team, you will provide specialist medical and scientific strategic and operational input into core medical affairs activities.Key Responsibilities:Develop and...

Job DescriptionJob DescriptionWork Location: Irwindale, CaliforniaSalary Range: $80,000 - $140,000 depending on related working experienceJob Type: Full-Time OnsiteOur Company:Founded in 2010, iHealth Labs is dedicated to empowering people to live healthier lives. The company is a leading provider of cloud-connected medical devices, personal health care...

Job SummaryAt BioSpace, Inc., we are seeking a highly skilled Medical Director/Scientific Director to join our team. This individual will be responsible for providing strategic medical and scientific input into core medical affairs activities, including health-care professional and provider interactions, generation of clinical and scientific data,...

Senior Regulatory Operations Associate Contractor (Publishing) Like the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description. Must be local for Florham Park, NJ (Hybrid 2-3 days onsite) 12-month contract (renewable) Senior Regulatory Operations Associate...

Job DescriptionPurpose:The Safety Statistics Group at AbbVie is a critical component of Data and Statistical Sciences. As a Senior Manager, you will be part of collaborative teams with Pharmacovigilance, Patient Safety, Statistical Programming, Clinical Statistics, Regulatory Affairs, and Medical Writing. Your focus will be on evaluating, interpreting, and...