Regulatory Coordinator: Average Salary in New Jersey in 2024

SMBC is seeking a self-motivated and diligent professional for the associate position within the Controllers - Regulatory Reporting Analysis Group. Assist in the preparation of the quarterly regulatory reports. Assist in maintaining proper controls and documentation associated with regulatory report...

What will you be doing?\n\nSingle point-of-contact for the assigned Audio-Visual program (s)\nProvide weekly program status updates to management and customer stakeholders\nProvides escalation for project managers and the client\nProvides cross-regional and/or specialty coordination and ensures cons...

The individual will be partnering with Regulatory Reporting Analysis team members and business stakeholders to assist with the automation efforts across all regulatory reports. Partner with Regulatory Reporting Analysis team members to understand current reporting procedures and manual processes per...

Prepares and maintains project plans, tracks project progress, and prepares reports for clients or project stakeholders. Currently the Center for Natural Resources has received funding for a few new projects and this position is needed in allocating a skilled resource to them. Works with communiti...

DOWNLOAD OUR CODE OF CONDUCT 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. Publis...

Perform other regulatory tasks as assigned. Regulatory, Legal/Compliance, Medical, Marketing, Creative Agencies. ...

Newark Community Solutions seeks an Intake and Compliance Specialist as part of its Eviction Diversion Initiative. Reporting to the Senior Resource Navigator, the Intake and Compliance Specialist is responsible for identifying participants, monitoring the tenant hotline, completing intake screenings...

CMC Regulatory Affairs Specialist performs regulatory assessment of changes. Interpreting the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission form process. Reviews regulatory submissions to ensure all aspects of global regulatory and CMC compl...

This role will report directly to the VP of Global Regulatory Affairs. This list is not totally inclusive, and the person will be expected to complete tasks reasonably requested by the VP of Global Regulatory Affairs. Under direction from the VP of Global Regulatory Affairs, the. R&D, Regulatory...

The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review process and leadi...

In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...

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. This role has high visibility within the Somerset site and the...

Summary:Program Manager is responsible to support & manage the day-to-day activities for new product launch projects with the objective to successfully commercialize and launch new products for SUN pharma. Area of Responsibility:Coordinate, Support & Align with Senior Program Leads on the Overall La...

They will be taking over the project management process and create processes within a new team. ...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Compile, prepare, and review regulatory submission to US and EU. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input for responsible countries/region fo...

Compliance and Regulatory Specialist. Bachelor’s degree with at least 5+ years of experience working in the pharmaceutical industry in Quality/Regulatory Compliance, Quality Assurance, Quality Management Systems or associated pharmaceutical manufacturing related function. Associate degree or High Sc...

Maintains service programs full adherence to relevant service programs manuals. Conducts weekly program visits and supervision with program supervisors. Coordinates all necessary team meetings for the program. Develops, modifies, and/or recommends necessary amendments of the service plans to Support...

Provide consultation and advice to regulatory specialists regarding change control and product development. Offer regulatory direction and interpretation on team activities. Apply regulatory knowledge to support product-related activities. Prepare regulatory submissions and registration documents fo...

Rutgers, The State University of New Jersey is seeking a Senior Program Coordinator for Rutgers Residence Life. Leads and coordinates the on-going evaluation process for all the selection programs, as well the undergraduate and graduate performance appraisal process. Union Description URA-AFT Admini...

The Project Coordinator will need to demonstrate extremely strong organizational skills and maintain meticulous records of all their projects and assist the Project Managers with their records. The Seasonal Project Coordinator is a position to assist the Project Managers. The Project Coordinator wil...

In addition, the Program Coordinator will collect and use data to inform ongoing monitoring and improvement of the program. The Program Coordinator will assist the Program Director by handling administrative tasks and serving as the liaison with partnering agencies and organizations. The full-time P...

As we further expand our US presence, we have a new opportunity for a proven Project Manager to join our highly collaborative team, to oversee all commercial areas of our Audio-Visual projects and to act as the clients’ primary contact ensuring all contractual commitments are met. Oversee project In...

The project coordinator works across groups, aligning internal team members and external stakeholders and may coordinate project schedules, arrange support services, order supplies, and track progress. Works in collaboration with various project leadership and is a project champion to ensure the suc...

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forens...

As a member of the NERC Compliance Group, you will perform governance and oversight of PSEG’s compliance with the NERC Critical Infrastructure Protection (CIP) Reliability Standards. Bachelor’s degree in Engineering, Compliance, Computer Science or a related field with a minimum of 4 years of equiva...