Internal Affairs Investigator Jobs in Edison, NJ

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Remote-Medical Director - CV Renal  

Novo Nordisk - Plainsboro Township, NJ 08536

internal relationships within Novo Nordisk Inc. and Global HQ. Key internal relationships include Field Medical Affairs, Medical Strategy & Operations, Medical Information, Publications, Clinical Directors

from: Pharmadiversityjobboard.com - 26 days ago

Medical Director - Clinical Development & Research  

Novo Nordisk - Plainsboro Township, NJ 08536

. Internal relationships include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs, Regulatory Affairs and other NNI skill areas. External relationships include expert

from: Pharmadiversityjobboard.com - 20 days ago

Medical Director, Bladder - Global Medical Affairs Oncology  

Johnson & Johnson - Raritan, NJ

investigators. Importantly, they will lead the internal study working group for this global study, working with R&D regional Medical Affairs colleagues. Qualifications Qualifications This position requires USD 187,000.00 - 322,000.00 per year

from: Dice.com - 6 days ago

Scientific Director, Medical Affairs- CNS/Psychiatry at AbbVie  

AbbVie - Florham Park, New Jersey

with internal stakeholders as they relate to ongoing medical affairs and clinical projects. Serve as the voice of the patient and HCP in all activities. + Has overall responsibility for oversight of the Medical

from: HealtheCareers.com (+1 source) - 9 days ago

Medical Director, Medical Affairs- CNS/Psychiatry  

AbbVie - Florham Park, NJ

and medical activities with internal stakeholders (i.e., commercial, clinical operations, discovery, statistics, regulatory, etc...) as they relate to on-going medical affairs projects. Serves as the scientific

from: Pharmadiversityjobboard.com (+1 source) - 9 days ago

Director (Principal Scientist), Regulatory Affairs Liaison- Vaccines and Infectious Disease (Hybrid)  

Merck - Rahway, NJ 07065

to external agencies and investigators. Represents Global Regulatory Affairs (GR) within internal committees to provide regulatory advice and approval according to the committee charters (therapeutic area

from: Pharmadiversityjobboard.com - 28 days ago

Manager, GCP Quality Assurance  

Aquestive Therapeutics - Warren, NJ

trials in biotech or pharma required. Experience auditing GCP vendors who provide clinical trial and nonclinical study services, internal GCP processes and documents, and clinical investigator sites

from: careerbuilder.com - 24 days ago


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