Regulatory Consultant: Average Salary in New Brunswick, NJ in 2024

Excellent employment opportunity for a Regulatory Affairs Consultant in the Somerville, NJ area. Represent Regulatory Affairs by attending project team meetings, providing regulatory strategies, reviewing project documentation, and participating in design control activities, as scheduled. Submit not...

Our practitioners help organizations identify the regulatory and industry changes impacting their business and implement effective and efficient regulatory and risk reporting frameworks and processes including regulatory reporting, reporting governance, risk management, process and controls manageme...

Pharma, Biotech, Medical Devices) Regulatory Affairs with experience in the areas of Regulatory Strategy or Regulatory Development and Regulatory Operations. Experienced Life Sciences Domain / Business or Transformation Consultants driving Advisory Services and Delivery, for pharmaceutical and medic...

Pharma, Biotech, Medical Devices) Regulatory Affairs with experience in the areas of Regulatory Strategy or Regulatory Development and Regulatory Operations•Strong experience Life Sciences Regulatory areas, with Consulting / Advisory company, Global pharmaceutical or medical devices company / IT Com...

Regulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies, government agencies as needed to develop harmonized policies, procedures and work instructions for ...

The Geotechnical Project Manager is responsible for the management of clients and projects, supervising the preparation of geotechnical engineering reports, geotechnical engineering calculations, and special inspections in support of: borings, test pits, earth retaining structures (temporary and per...

Position: Regulatory Affairs Manager. Prepare and submit CTAs within the EU Clinical Trial Integrated System (CTIS) and MHRA Integrated Regulatory Submission (IRAS) submission portals in accordance with regulatory requirements, using Submission Management tools and an EDMS system. Assist with develo...

Regulatory Compliance Specialist (14450840). Senior Regulatory Compliance Specialist. Senior Regulatory Compliance Specialist. Supplier Quality, Regulatory Compliance, DEA, and QMS. ...

Join Our Winning Team - Sales Agent Position with the Pappas Agency. Our first-time agents can earn up to $75-150K per year, even with no sales experience. In addition to a competitive commission structure, we offer up to $7,000 cash bonuses and an all-expense-paid trip worth $8k based on sales in t...

The Senior Manager, Regulatory Affairs will handle publishing and coordinating tasks for Global RA submission activities. Review and track the archiving of global eCTDs , paper submissions and Health Authority correspondences using Regulatory Affairs systems/tool. Publish, review, submission and arc...

The Labeling Specialist supports the development of labeling activities for all regulatory submissions. This individual works cross-functionally with internal and external departments on Regulatory Affairs labeling related issues. Effective collaboration with Regulatory Affairs, CMR, Supply Chain, a...

SAP Program Management Resource will assist in various SAP/ERP programs/projects related to technology and service transitions. Reporting to SAP Delivery Head, SAP Engagement Director/Program Manager is responsible for the planning, execution and management of complex and large transformation engage...

As the Manager of Regulatory Affairs, this role advises the research, creative, application and commercial departments or customers on the safe use, regulatory compliance, regulatory strategy or advocacy for ingredients and products. In a regulatory landscape that is continuously evolving and with o...

Responsible for ensuring that the program is aligned to enterprise strategic business objectives and program deliverables meet stakeholder expectations. Collaborate with the project manager(s) in the management of overall resource allocation and capacity planning for the projects within the program....

The requirement is for 3 Regulatory Affairs Specialist. The candidates will work with client & Our client's teams to deliver best in-class solutions for regulatory submissions. Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to re...

Strong understanding of data sources, such as clinical trial data, electronic health records, and other healthcare databases. This position focuses on assisting with analyzing data and deriving insights from clinical and safety data sources to generate evidence and support decision making across the...

As a Compliance Program Support Analyst on the Compliance Program Support team, you will collaborate with subject matter Compliance Officers in working with insurance and reinsurance business and support functions to create and maintain controls over the various legal and regulatory compliance and e...

Reporting to the Senior Manager of Museum Projects & Strategic Initiatives, and supporting the work and leadership of the Campus Art Steering Committee (co-chaired by the Art Museum Director and the University Architect), the position will project manage the care of existing campus art collectio...

Must have proven track record in managing multi-year projects and/or programs; 3 years of experience utilizing leadership and managerial skills, working with diverse teams across multiple geographies. Consolidate status reports across multiple ongoing projects into a program/portfolio view for consu...

Regulatory Affairs Manager/Sr Manager. Regulatory Affairs Manager/Sr Manager - CGP - Oncology Trials - Remote US. You'll serve as the primary point of contact for all regulatory responsibilities associated with assigned projects and represent regulatory function at cross function discussions. Provid...

Export Compliance Specialist - Contractor position. Provide Export compliance support to all sites and locations. Assessments & compliance with pertinent Export laws, regulations and guidelines mandated by government. Support analysis, improvement, and implementation of the Export compliance program...

As a Strategic Initiatives Program Manager, you will immerse yourself in key projects that directly impact our business, collaborate with leaders across departments, and manage high-level relationships with both internal and external stakeholders. Project and Program Management experience with an ab...

Years of experience in business process analysis / business process design activities and concepts preferred. Become functional/technical expert on LIMS and Biovia eLN archive (system features, system functionality, access/security controls, master data and understanding of the business processes th...

We are seeking those who have a passion for using data, analytics, and insights to drive decision making, that will allow us to tackle some of the world’s greatest health threats. Within our commercial Insights, Analytics, and Data or…. ...

The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. The ideal candidate must be agile and have well-developed orga...