Drug Regulatory Affairs Jobs in New Jersey

Shionogi Inc. - Florham Park, New Jersey

, medical and regulatory affairs, and commercial teams to drive successful drug development programs. Provide strategic guidance and decision support to senior management on project priorities, resource

from: resume-library.com - 10 days ago

Merck - Rahway, NJ 07065

Team. Strong organizational, time management, and multi-project coordination skills Broad knowledge of Clinical Development and Regulatory Affairs requirements Ability to multi-task, work independently

from: Pharmadiversityjobboard.com - 13 days ago

Johnson & Johnson - Raritan, NJ

data review, including medical data review, coding, in conjunction with other clinical team members. OTHER RESPONSIBILITIES / DETAILED DUTIES: Assists Regulatory Affairs in the development of drug USD 135,000.00 - 232,300.00 per year

from: Dice.com - 17 days ago

Cloudious LLC - Princeton, NJ

experience in regulatory affairs (e.g., 3-5 years) Key Competency Required: Expert understanding of policy, laws, regulations, and guidelines as they apply to U.S. FDA for drug development and approval. Expert

from: Dice.com - 19 days ago

Merck - Rahway, NJ 07065

with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects. Assist the Executive Director in ensuring

from: Pharmadiversityjobboard.com - 26 days ago

Rahway, NJ

Affairs, the Specialist has the following main responsibilities: · Drug Listings - Maintain and update drug listings for new marketed US Pharmaceutical products (including but not limited to establishment $73,788 - $110,000/Year

from: careerbuilder.com - 5 days ago

Daiichi Sankyo, Inc. - Bernards, NJ

Years of proven experience in a regional regulatory lead role 7 or More Years of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs Knowledge of IND, NDA/BLA

from: careerbuilder.com - 5 days ago

Daiichi Sankyo, Inc. - Bernards, NJ

. Experience Qualifications: 10 or More Years in the pharmaceutical industry required. 7 or More Years in regulatory affairs Experience in providing regulatory strategic input into the drug development process

from: careerbuilder.com - 12 days ago

Daiichi Sankyo, Inc. - Bernards, NJ

. Experience Qualifications: 10 or More Years in the pharmaceutical industry required. 8 or More Years in regulatory affairs Experience in providing regulatory strategic input into the drug development process

from: careerbuilder.com - 13 days ago