Regulatory affairs jobs in Bridgewater, New Jersey (NJ) State

This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the devel...

Associate Director, US Advertising and Promotion, Global Regulatory Affairs. Trusted Staffe is partnering with a renowned global healthcare and pharmaceutical company based in Bridgewater, NJ, to find an experienced and strategic Associate Director of US Advertising and Promotion. ...

Regulatory Affairs Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in...

The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory agencies. Mini...

This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the devel...

Leadership capabilities and ability to work with cross-functional team. This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunolog...

The Senior Director, Clinical Development Medical Affairs is responsible for the strategic direction, planning, execution, and oversight of our clinical development programs, ensuring they meet the highest scientific and regulatory standards. The Senior Director, Clinical Development Medical Affa...

Provides scientific, technological and medical knowledge and expertise for the clinical research aspects of registration activities with a working knowledge of regulatory affairs, in the development of the project strategy and the clinical development plan (CDP). The Senior Director CDMA will int...

This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. ...

The Senior Director, Clinical Development Medical Affairs is responsible for the strategic direction, planning, execution, and oversight of our clinical development programs, ensuring they meet the highest scientific and regulatory standards. The Senior Director, Clinical Development Medical Affa...

The Associate Director, Advertising and Promotion, Prescription Drug Products, reviews, approves and monitors prescription drug product advertising and promotional labeling pieces for compliance with regulatory agency requirements. ...

The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory agencies. Expe...

Job title:  Head of U.S. Medical ImmunologyLocation: Cambridge, Massachusetts                 Bridgewater, New JerseyAbout the JobAre you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills c...

Build and manage cross-functional teams/scrum teams, including quality, legal, and regulatory affairs. * Define KPIs and value propositions, and act based on impact assessments. About You * Advanced ...

Education and Experience: • BS/BA degree in a relevant scientific discipline required. Advanced ... biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs ...

Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. At Kelly, we believe that the more inclusive we are, the better services we can provide. Kelly® Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New Jersey. ....

Senior Director, Global Regulatory Affairs Strategy The position will provide regulatory affairs strategic leadership for the company and novel drug development programs. Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory...

The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review process and le...

DOWNLOAD OUR CODE OF CONDUCT The Senior Manager, Regulatory Affairs will handle publishing and coordinating tasks for Global RA submission activities. Review and track the archiving of global eCTDs , paper submissions and Health Authority correspondences using Regulatory Affairs systems/tool. Pub...

More Years of relevant pharmaceutical experience including experience within Regulatory Affairs. Experience with communicating the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leadership team and other governing bodies required. Ensure global regulatory...

DOWNLOAD OUR CODE OF CONDUCT The Senior Manager, Regulatory Affairs will handle publishing and coordinating tasks for Global RA submission activities. Review and track the archiving of global eCTDs , paper submissions and Health Authority correspondences using Regulatory Affairs systems/tool. Pub...

Global Regulatory Affairs Operation（Sr. This position belongs to Global regulatory affairs department, serving the global Market which encompasses China US, EU, AUS and others. This role requires a detail-oriented professional who can oversee all regulatory affairs and quality assurance activitie...

Manager of Regulatory Affairs Strategy to join their team. Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. This role is responsible for developing, implementing, and leading short/long term global regulatory s...

The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval conditions. Under the direction of Regulatory Affairs management, participate in drug development from early stage development through final formulation, ensuring compliance with princi...