Drug Regulatory Affairs Jobs in Raritan, NJ

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

Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States

and through strategic partnerships with manufactures from around the world. JOB SUMMARY: The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval

from: linkedin.com - 11 days ago

GForce Life Sciences - Princeton, NJ, United States

preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual

from: linkedin.com - 6 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 - 6 days ago

GForce Life Sciences - Princeton, NJ, United States

preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual

from: linkedin.com - 8 days ago

Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States

regulatory affairs operations. Knowledge of eCTD publishing systems and standards, EDMS technology and related publishing tools. Working knowledge of US FDA (OGD/CDER) e-submission requirements. Strong written

from: linkedin.com - 15 days ago

Experis - Rahway, New Jersey

regular updates to management and escalates issues. MAJOR ACTIVITIES AND RESPONSIBILITIES: With the support and guidance of the Executive Director of US Regulatory Affairs, the Specialist has the following

from: resume-library.com - 3 days ago

Proclinical Staffing - Morristown, NJ, United States

Regulatory Affairs representative, you will work with brand on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies

from: linkedin.com - 16 days ago

i-Pharm Consulting - Trenton, NJ, United States

and build out the full R&D organization including clinical development, clinical operations, regulatory affairs, biometrics, medical affairs and drug safety Oversee design and execution of global clinical

from: linkedin.com - 21 days ago

Englewood Lab, Inc - Totowa, New Jersey

Responsibilities: Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits. With the assistance of Head of R&D (or designee), create and collate product master files

from: resume-library.com (+1 source) - 3 days ago