Drug Regulatory Affairs Jobs in Rahway, NJ
Clinical Dynamix - Jersey City, NJ, United States
research labs (CROs). This individual will partner with CMC, Clinical, Regulatory Affairs, and other corporate stakeholders to ensure Company’s clinical and commercial products follow cGMP framework
from: linkedin.com (+1 source) - 30 days ago
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
Register your RESUMEfrom: resume-library.com - 11 days ago
HUMAC INC. - 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 Depends on Experience
from: Dice.com - 7 days ago
Pfizer - New York City, New York
potential of our existing and future commercially available medicines. + The role will partner closely with Pfizer Oncology stakeholder groups (including Research, Early and Late Development, Regulatory
from: HealtheCareers.com - 24 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 - 18 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 - 20 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 - 6 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 - 13 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 - 14 days ago
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