- Prime Therapeutics (Trenton, NJ)
- …ensure fee schedule revisions align with Supply Chains COGS strategies for specialty drug management + Lead and implement network initiatives by facilitating and ... from negotiation of all terms, ensuring Prime and Pharmacy compliance and document retention aligning with Prime's Record Information Management (RIM) policies… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …of drug development principles and clinical trial implementation and management . + Complete understanding of the global regulatory requirements. + ... a major impact on human health. OPDC develops promising drug candidates, starting with clinical trial management ,...with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible… more
- Bank of America (Pennington, NJ)
- Merrill Onboarding & Maintenance Account Management Ops Representative Pennington, New Jersey;Tampa, Florida **To proceed with your application, you must be at least ... be at least 18 years of age.** Acknowledge (https://ghr.wd1.myworkdayjobs.com/Lateral-US/job/Pennington/Merrill-Onboarding Maintenance-Account- Management -Ops-Representative\_25043824-2) **Job Description:** At Bank of America, we are… more
- Sanofi Group (Morristown, NJ)
- …statistics + Knowledge of regulatory environment + Proficient in document management systems and authoring platforms **Professional Attributes:** + Strong ... be critical in helping our teams accelerate progress. Global Medical writing and Document management serves to generate timely, high quality, cost effective and… more
- Sanofi Group (Morristown, NJ)
- …Study Units, and investigators + Contribute to the clinical part of Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc.) and ... appropriately with all function stakeholders (eg clinical operations, project management , Patient Safety and Pharmacovigilance, regulatory , Finance, Scientific… more
- Sanofi Group (Morristown, NJ)
- …generating submission content plans, submission tracking, communication and document management . + Contribute to internal regulatory processes and procedures ... to be used alone or in combination with a drug product, leading regulatory efforts in the...control deliverables. + Contribute to product development and lifecycle management planning. Provide regulatory impact assessments for… more
- Sanofi Group (Morristown, NJ)
- …stages of submission development. + Expertise in the eCTD process, document management environments/systems, publishing tools and submission software. + ... was possible. Ready to get started? **Main Responsibilities:** + Applies project management skills and regulatory knowledge for global submission types, from… more
- Sanofi Group (Morristown, NJ)
- …Clinical Study Units, and investigators + Responsible for the clinical part of regulatory documents, Common Technical Document for submission to regulatory ... + Clinical trial or pharmaceutical experience in ophthalmology + Knowledge of drug development, ocular gene therapy, regulatory strategy + Good networking… more
- Bank of America (Jersey City, NJ)
- …(CCP), and Value at Risk (VaR). GMRA also develops analytical tools to support regulatory , audit, and internal risk management needs for Global Markets. This ... Independent Testing (EIT) are sub-lines of business within Global Risk Management (GRM). Collectively, they are responsible for developing a consistent and… more
- J&J Family of Companies (Raritan, NJ)
- …leading continuous improvement projects is required. + Experience working with document management systems is required. + Experience effectively/appropriately ... Industry Analysis, Legal Support, Mentorship, Organizing, Product Licensing, Public Policies, Regulatory Affairs Management , Regulatory Compliance, … more