Regulatory Expert - Princeton

Provide strategic leadership for Quality Assurance programs across U.S. operations ensuring compliance with applicable global regulations and industry standards. · ...

We are seeking a detail-oriented and strategic professional to play a pivotal role in supporting enterprise-wide regulatory inspections.Our team values proactive project management and the ability to ensure accurate and compliant documentation, making this position integral to up ...

We are seeking an experienced professional to provide expert regulatory affairs support focused on advertising and promotional review activities. Our team places particular emphasis on compliance with evolving FDA regulations, · Conduct comprehensive regulatory reviews of promoti ...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds... · ...

· SystImmune is seeking an experienced Director/Sr. Director/Executive Director for its Clinical Regulatory Affairs team to drive regulatory strategy and execution within SI Project development teams. · Integrate scientific, medical and regulatory perspectives to drive developme ...

We offer an opportunity for you to learn and grow while making significant contributions to the company's success.The Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department in all aspec ...

We would like to fill the following permanent vacancy in an hybrid working model in Princeton as soon as possible · Your role · Contribute to medical and scientific strategy for the clinical development of ITM radiopharmaceutical products... · ...

We are seeking a Regulatory Affairs Professional who will serve as an internal expert on U.S. FDA regulations governing the promotion of prescription drug and biologic products.The ideal candidate will have experience in drug, biologic and/or combination products in Regulatory Af ...

We are seeking an experienced Senior Statutory & Regulatory Reporting Specialist to join our Finance team and support statutory and regulatory reporting across the United States and Canada. · Pregare and file quarterly and annual statutory financial statements for U.S. regulatory ...

Kardigan is seeking an experienced Director of CMC Drug Substance Development to oversee the development of its pipeline and portfolio across small molecules and oligonucleotides. · Cross-functional collaboration with drug product development teams. · Maintain awareness of evolvi ...

We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone metastases. · ...

Our client is seeking a Medical Director or Senior Medical Director to provide scientific and clinical leadership across key development programs. · ...

Dice is seeking Quality Assurance Analyst for SGS Consulting in Princeton. · ...

The Executive Director Analytical Sciences will provide strategic and operational leadership for all analytical activities supporting the development registration and commercialization of the Company's lead bispecific antibody product. · ...

Our client, New Jersey Hospital Association (NJHA), is a mission-driven trade organization, · supporting hospitals and other healthcare providers across the state to improve the health of the people of New Jersey.NJHA's Health Information Management (HIM) division is seeking a Se ...

The Sr. Director, Clinical Operations provides strategic and operational leadership across all clinical functions to advance the company's rare disease portfolio. · This leader oversees Clinical Operations, ensuring scientific excellence, regulatory compliance, and operational ef ...

Responsible for planning and implementing computer system validation protocols of GxP computerized systems. · ...

We are looking for a Senior Director to lead our global regulatory strategy in Neuroscience. · This is an exciting opportunity to join our team and contribute to the development of innovative medicines that transform patients' lives. · You will be responsible for developing globa ...

We're looking for a Senior Director, Global Regulatory Lead Neuroscience to join our team.Bristol Myers Squibb is an equal opportunities employer. · Develop global therapeutic regulatory strategies and operational plans for identified investigational and marketed products. · Asse ...

We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone metastases. · Competitive base salary. · Comprehensive health benefits, including a medical pl ...