Search Results: 784 vacancies

 ...Job Overview: RWJBH is seeking a Coordinator Regulatory for our Community & Government Affairs department at the New Brunswick campus. Qualifications: Required: Minimum of five years of experience in clinical practice Knowledgeable about federal, state,... 
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Main Hospital - New Brunswick

New Brunswick, NJ
more than 2 months ago
 ...Job Description AVP/VP Underwriting Governance- Westfield Specialty Job Description: Create, manage, and execute quality underwriting review strategies/plans across multiple lines of business, including external delegated underwriting authorities (MGAs).... 
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Westfield

Berkeley Heights, NJ
2 days ago
 ...Responsibilities: Provides administrative support for regulatory affairs manager Provides RA support for change control projects and sustaining activities Conducts regulatory assessments and determines need for re-registration for proposed device changes... 
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Worldwide

Katalyst HealthCares and Life Sciences

South Plainfield, NJ
2 days ago
The CMC Regulatory Affairs Specialist is responsible for for a subset of programs at the IOPS facility. Evaluate proposed changes to IOPS documents and procedures to determine regulatory impact.E ssential Duties and Responsibilities include, but are not limited to, the... 
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Regeneron Pharmaceuticals Inc.

Basking Ridge, NJ
4 days ago
 ...pharmaceutical industry required. ~8 or More Years in regulatory affairs ~ Experience in providing regulatory strategic input into the...  .... ~ Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of regulations... 
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Daiichi Sankyo, Inc.

Basking Ridge, NJ
2 days ago
 ...pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to Regulatory Affairs, Director, Associate, Regulatory, Product Development, Business Services, Compliance... 
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Worldwide

Catalent, Inc.

Somerset, NJ
2 days ago
 ...enrollment application from new and existing providers through all stages to enroll or re-validate the facilities/providers with government payers. This will include a compilation of confidential data and communications. Will manage the external consultant ensuring accuracy... 
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Hackensack Meridian Health

Edison, NJ
5 days ago
 ...advertising and promotion - related processes and procedures to enhance efficiencies and compliance. Works closely with the Regulatory Affairs labeling group regarding package insert changes to assess and determine the impact of proposed labeling changes on product... 
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Bausch Health

Bridgewater, NJ
2 days ago
 ...in South Plainfield currently has an opening for a Regulatory Affairs Specialist - Pharma YOUR ROLE & RESPONSIBILITIES * Supporting...  ...North America, Inc. and its subsidiaries use E-verify, a government-run, web-based system that allows employers to confirm the eligibility... 
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Brenntag

South Plainfield, NJ
4 days ago
The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Lead for a prominent Pharmaceutical client of ours. This position is in Bridgewater, NJ (Hybrid Role). Details for the position are as follows: Job Description:... 
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Flexible hours

The Fountain Group LLC

Bridgewater, NJ
3 days ago
 ...~10+ years' experience in Global Regulatory affairs, CMC submissions. ~ Knowledge on Insights and regulatory affairs. ~ Develop the detailed project plan ~ Kickoff the project with full project team including IT, Validation and Business participants ~... 
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The Dignify Solutions LLC

Raritan, NJ
1 day ago
 ...other research areas centered around rare diseases and immune disorders. Summary The Senior Director, Global Oncology Medical Affairs is responsible for developing the Global Medical Affairs (GMA) strategy and tactical plan as part of the Global Brand Strategic Plan... 
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Local area

Daiichi Sankyo, Inc.

Basking Ridge, NJ
5 days ago
 ...management as needed. Competencies and Capabilities This individual is expected to competently and confidently represent Regulatory Affairs as a key member of cross-functional RC teams for assigned, as well as for all verbal and written communications with OPDP/APLB... 
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Sanofi

Bridgewater, NJ
4 days ago
 ...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 conditions. A Senior Associate is expected to have a strong... 
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Overseas

Breckenridge Pharmaceutical Inc

Berkeley Heights, NJ
5 days ago
 ...required for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global locations or contract manufacturing organizations (CMOs), or alliance partners. He/She... 
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Spectraforce Technologies Inc

Bridgewater, NJ
5 days ago
 ...are met and that client deliverables are successfully executed. Additionally, the Data Management team designs and implements data governance and standardization principles to be utilized across the DTC and HCP measurement business. Likewise, the team supports several... 
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IQVIA, Inc.

Warren, NJ
4 days ago
 ...well as other research areas centered around rare diseases and immune disorders. Summary The Director, Global Oncology Medical Affairs, Evidence Generation role is responsible for co-leading a cross-functional Evidence Generation Team and developing an Integrated Evidence... 

Daiichi Sankyo, Inc.

Basking Ridge, NJ
1 day ago
 ...leaders we produce for the industry. Will you be next? Job Details: Are you passionate about Data? Do you believe that data governance is critical for organizations to use data responsibly and efficiently for realizing business goals? Are you ready to take charge... 
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3 days per week

Axtria, Inc.

Berkeley Heights, NJ
1 day ago
 ...support for all aspects of Global Clinical Operations with a high degree of quality in the execution of all Global Oncology Medical Affairs (GOMA) Company Sponsored Studies (CSS) and Medical Access/Expanded Access (MAP)/(EAP)activities in adherence to Good Clinical... 
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Daiichi Sankyo

Basking Ridge, NJ
5 days ago
Overview/Risks: Responsible for supporting R&D activities by conducting experiments related to product and process development, preparing different allograft tissue forms based on protocols or SOPs, preparing test samples, developing and executing test protocols, and...

MTF Biologics

Edison, NJ
2 days ago