Regulatory affairs associate jobs in East Orange, NJ

The Position The Associate Director (Associate Principal Scientist), Organon Manufacturing & Supply.. Direct experience in Regulatory CMC. Demonstrated experience driving change initiative projects. Who We..

And commercial teams and leads regulatory activities associated with planning, authoring, compiling, and.. ORGANIZATION STRUCTURE The Manager, Regulatory Affairs reports into the Director Regulatory Affairs or..

Summary Our client, a growing pharmaceutical company, has engaged GForce to provide a CMC Regulatory Affairs Manager Consultant. The role will be focused on providing CMC regulatory strategy..

Responsibilities Deputy Therapeutic Area Head Support the Regulatory Affairs Therapeutic Area Head for.. Directs due diligence activities related to regulatory affairs and directs activities associated with..

On Board Scientific is hiring a Regulatory Affairs Assistant!For immediate consideration please send.. st shiftBenefits Compensation. per hour based on previous experience The Regulatory Assistant needs to..

FDA EMA) guidelines for NDA MAA IND or CTA interactions. Manage the regulatory activities for multiple.. Support the development of regulatory strategy and update strategy based upon regulatory changes..

The company handles research, clinical development, sales, marketing, medical affairs, supply chain, and.. Handles other administrative tasks as assigned. Qualifications. Associate Degree in Office..

The company handles research, clinical development, sales, marketing, medical affairs, supply chain, and.. The Director, Regulatory Affairs (Early Development) provides strategic global regulatory guidance to..

Paid time off. Parental leave. Vision insurance. Job Summary The Regulatory Affairs Specialist is.. The role assists the Regulatory Manager and other associates within the Regulatory Department and works..

Regulatory Affairs Project Manager Position SummaryCatalent is a global, high growth, public company and.. The Regulatory Affairs Project Manager is responsible for ensuring that the company aligns with all of..

Job Description. POSITION Nonclinical Regulatory Document and Scientific Writer DEPARTMENT Nonclinical.. Regulatory submissions will span across all therapeutic areas (cancer, immunology, neurology etc..

Senior Regulatory Associate. Hybrid, NJ (2 3 days a week) I am currently partnered with a global.. Responsibilities. Act as the Regulatory Affairs lead on assigned projects, ensuring the completion..

For more information visit. or LinkedIn vantagePOSITION SUMMARYRegulatory Affairs Senior Manager is.. This position will report directly to the Global Director Regulatory Affairs. The person will be..

Make It With Pride.The Sr. Scientist II will u execute the scientific affairs strategy for your.. You advocate for our regulatory and scientific positions to promote the removal of technical barriers..

Disease. As the Director, Regulatory Affairs. Advertising, Promotion and Regulatory Compliance you will.. The Director will also serve as the company subject matter expert for regulatory review of advertising..

Description templates and other group health plan documents.Perform additional tasks and lead additional work streams, from time to time and upon request, concerning the regulatory regime or..

Job DescriptionThe PositionReporting to the Director or Executive Director in Organon Regulatory CMC New.. The Associate Principal Scientist may also support project team goals and organizational initiatives, on..

No Honor Period. Life of search The primary responsibility of this role, as Associate Director Global.. Strong management skills are a plus. Regulatory affairs All your information will be kept confidential..