Drug Regulatory Affairs Jobs in Berkeley Heights, NJ

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Senior Regulatory Affairs Associate  

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 - 8 days ago

Senior Pharmacovigilance Associate  

Tandym Group - Florham Park, NJ, United States

per device safety reporting requirements In-depth knowledge of the Drug Development process, Signal Detection, and Regulatory Affairs In-depth knowledge of Domestic and Global Safety regulations Profound

from: linkedin.com - 5 days ago

Senior Principal Scientist, Clinical Research, Hematology/Lymphoma  

Merck - Rahway, NJ 07065

, the Senior Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs

from: Pharmadiversityjobboard.com - 14 days ago

Head of Data Engineering, Healthcare & Life Sciences  

Fractal - New York, NY, United States

of drug commercialization, patient claims, real-world data, EHR/EMR, market access, medical affairs, and the regulatory landscape. Ability to manage a portfolio of 40-50MN revenue enterprise technical

from: linkedin.com - 3 days ago

Senior Director, Translational Medicine and Clinical Pharmacology  

SUN PHARMA - Princeton, NJ, United States

clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations) Provide clinical

from: linkedin.com - 17 days ago

Principal Scientist, Hematology-Oncology  

Merck - Rahway, NJ 07065

the activities of Clinical Scientists in the execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage

from: Pharmadiversityjobboard.com - 14 days ago

GPV Submission Specialist  

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 - 5 days ago

Director, Regulatory Affairs Strategy  

NS Pharma, Inc. - Paramus, NJ, United States

and other health authority guidances/guidelines. Experience in rare disease/accelerated approvals preferred. Regulatory Affairs Certification is a plus.

from: linkedin.com - 5 days ago

Senior Clinical Director  

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 - 3 days ago

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Senior Director, Regulatory Affairs - REMOTE  

Proclinical Staffing - New York, NY, United States

including significant experience in senior strategic role, including specific oncology investigational product experience The Senior Director, Regulatory Affairs will: Integrate strategic regulatory & drug

from: linkedin.com - 12 days ago


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