Regulatory Affairs Cro Jobs

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Sr. Project Manager, Clinical Project Management - Princeton  

Fahrenheit IT - Princeton, New Jersey, US

Director of Clinical Development and Sr. Director of Regulatory Affairs. Please send resume at rchugesnetwork.com or call Rose at 610-822-1256 for details. Strong managementnegotiating abilities to drive

from: neuvoo.us (+3 sources) - 4 days ago

Vice President, Regulatory Affairs  

San Francisco, California, US

teams to define contributions to submissions Lead the regulatory submission teams for projects assigned within defined time schedules and following established standards Represent the Regulatory Affairs

from: neuvoo.us - 2 days ago

Senior Clinical Scientist  

CSL Behring - King of Prussia, Pennsylvania

data monitoring committees, steering committees, etc. Collaborate with internal stakeholders (clinical operations, data management, statistics, safety, commercial, and regulatory affairs) to ensure

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

Senior/Principal Statistician - Irvine  

Irvine, California, US

activities, manuscripts, abstracts and regulatory communications. Oversee statistical work performed at CROs. Ensure compliance with regulatory guidelines. Provide input to CRF design, database development

from: neuvoo.us - 2 days ago

Product Safety Director - Rockville  

MacroGenics Inc. - Rockville, Maryland, US

functional area specialists including Clinical Operations, Regulatory Affairs, Biostatistics and Data Management, Contract Research Organizations (CROs), Data Monitoring Committees (DMCs) and other entities

from: neuvoo.us (+1 source) - 2 days ago

Director of Regulatory Affairs  

Connecta Pharma Resource - New York, NY

, commercial, and CROs on Regulatory Affairs related issues. • Serves as a primary liaison to US FDA, EMA, and other key market Health Authorities for assigned projects. • Defines strategies for, coordinate

from: ziprecruiter.com - 4 days ago

Associate Director, Regulatory Affairs Intelligence - Plainfield  

Plainfield, New Jersey, US

Regulatory Affairs experience in a pharmaceutical, biotechnology, contract research organization (CRO) or related environment OR equivalent experience and/or education. Special knowledge or skills needed

from: neuvoo.us - 2 days ago

Project Manager Drug Safety  

Raleigh, North Carolina, US (+2 locations)

in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance

from: neuvoo.us - 2 days ago

Director, Clinical Quality Assurance  

Seattle, Washington, United States

audits.. Work with clinical operations and regulatory affairs to review IND and NDA submission documents.. Responsible for ensuring submission data and documentation meets GCP guidelines.. Perform 125.000 - 150.000

from: jobleads.com - 8 days ago

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Principal Medical Writer - Morrisville  

Morrisville, North Carolina, US

writing projects Experience within a broad range of medical writing projects Additional qualifications in medical writing (AMWA, RAC, etc) is advantageous Broad regulatory affairs experience is an advantage

from: neuvoo.us - 2 days ago


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