Regulatory Affairs Associate II - Princeton, NJ

The Regulatory Operations Associate is responsible for publishing, QC, and transmittal of eCTD submissions, · as well as document formatting and report-level publishing. · ...

The Regulatory Operations Associate is responsible for publishing, QC, and transmittal of eCTD submissions, · e.g., using Acadia's eCTD publishing (IQVIA RIM Smart) and document management (Veeva Vault RIM), publish eCTD submissions and reports in alignment with health authority ...

Ensures a controlled documentation system record retention and information services including electronic records retention processes in accordance with regulatory requirements. · Maintains the technical and non-technical documentation change system · Interprets and enforces all d ...

The Associate Director Medical Affairs Operations is responsible for leading and managing all operational aspects of the Medical Affairs team to ensure the effective execution of strategic initiatives. · ...

The Associate Director will be responsible for helping build and execute global regulatory strategy objectives policies and programs pertaining to development marketing Acadia products including regulatory compliance for advertising promotion marketed products. · This role will s ...

The Associate Director helps build and execute global regulatory strategy for Acadia's products. · ...

The Associate Director Regulatory Affairs ROW is responsible for building and executing global regulatory strategy objectives policies programs pertaining to development marketing Acadia products including regulatory compliance advertising promotion marketed products. · ...

The Associate Director, Regulatory CMC, is responsible for contributing to/assisting with the development and implementation of global regulatory CMC strategies supporting investigational and marketed small molecules therapeutics worldwide. · Bachelor's degree in a life science o ...

This is an opportunity to work at Bristol Myers Squibb as an Associate Director in US Commercial Regulatory Affairs. The role involves applying complex scientific and expert regulatory advice to ensure promotional campaigns meet the company's objectives. · Provides regulatory adv ...

RK Pharma Inc is seeking a Regulatory Associate to work with our growing Regulatory Affairs Team as we scale towards commercial manufacturing in the next upcoming months. · ...

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. · We're changing lives for a living. Are you ready to make a difference? · The Associate Director, Medical Affairs Omnichannel Engage ...

This position is for an Associate Director of Medical Affairs Omnichannel Engagement at Novo Nordisk. The role will support the execution and governance of medical omnichannel engagement strategy across specific therapeutic areas.The ideal candidate will have experience in projec ...

The Associate Director, Global Medical Affairs Training is responsible for developing implementing continuously elevating Genmab training curricula supporting Health Evidence Outcomes Liaisons HEOLs cross-functional Medical Affairs partners. · Strategic Training Leadership Provid ...

We're changing lives for a living. Are you ready to make a difference? · ...

We are dedicated to building extraordinary futures by developing antibody products that change lives and the future of cancer treatment.The Associate Director Global Medical Affairs Training is responsible for developing training curricula supporting Health Evidence Liaisons and ...

We are hiring Regulatory Affairs Associate I. · Please let me know if you are interested or anyone who might be interested. Review formulas for compliance with local regulations in US and Canada. · Reviewing artwork for US and Canada Compliance. · Notifying products in US and Can ...

The Regulatory Affairs Associate manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · With input from the submission teams this individual establishes and maintains submission content planners and associated timelines ...

This is a Regulatory Affairs Associate position that requires a Bachelors level degree in Science or related field and strong working knowledge of Chemistry. · ...

We are hiring Regulatory Affairs Associate I. · Please let me know if you are interested or anyone who might be interested. · Client: Major Cosmetics Client · Position: Regulatory Affairs Associate I · Duration: 11+ months · Location: Clark, · NJ 07066 ...

The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets, vendors and administrative services. · Oversee daily office operations to ensure a safe clean functional and welcoming work environment. · Coordinate facility se ...