Regulatory Compliance Specialist: Average Salary in Salem, MA in 2024

The IACUC Regulatory Compliance Specialist has the overall responsibility for ensuring regulatory compliance within the areas of the animal care and use program that fall under the responsibility of the IACUC office. Job Description - IACUC Regulatory Compliance Specialist (3271795). Investigate and...

As an Environmental Compliance Specialist, you will partner cross-functionally to ensure the proper evaluation of project activity, pacing of consultant services, and compliance documentation. We are seeking an Environmental Compliance Specialist to join American Tower's U. You will collaborate with...

Compliance and Admissions Officer – Jupiter V Institute, Boston, MA. ...

Manager, Regulatory Affairs Labeling – Permanent – Georgia, North Carolina or Massachusetts. Proclinical is seeking a remote Manager, Regulatory Affairs Labeling for a global biopharmaceutical company with locations in Georgia, North Carolina and Massachusetts. The Manager, Regulatory Affairs Labeli...

The Regulatory Affairs Specialist will be responsible for the preparation, and review of regulatory documents for a novel veterinary product in various international jurisdictions. Assist in the development of regulatory strategies to facilitate timely approvals and optimize submission processes; wo...

Our award-winning client is seeking a Manager, Time Charging Compliance to join their team. In this critical role, you will play a pivotal role in safeguarding the client's financial integrity and ensuring compliance with all relevant regulations. Develop and deliver training programs to educate...

We are building a new type of regulatory intelligence platform using AI-driven workflows that enable Regulatory Affairs teams to work faster and more accurately when developing new clinical trial and regulatory filing strategies. Regulatory Affairs Informatics Specialist. We are seeking a skilled Re...

Cherry Hill Programs brings the magic to every experience by capturing moments that last a lifetime. In partnership with retail locations, tourist attractions, and destinations across North America, Cherry Hill Programs contributes millions of holiday and souvenir experiences for children and famili...

Join Takeda as a Manager, Global Regulatory Affairs CMC Submission Management where you will support the execution of regulatory CMC investigational, registration and post-approval tasks for assigned products. As part of the Regulatory Affairs CMC team, you will report to the Senior Manager GRA CMC ...

As an Associate Director, Global Regulatory Affairs Marketed Products you will define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. Demonstrates acceptable skills with increasing independence ...

As a Medicare Operations Compliance Manager. Compliance Program Development:. Create, maintain, and enhance the compliance program for Medicare Advantage Plans, including the development of policies, procedures, and controls. Develop a compliance roadmap that aligns with regulatory requirements and ...

Assistant Environmental Project Manager. This individual will interact with clients and help manage projects that require site characterization; due diligence assessments; environmental investigation related to soil, groundwater, and vapor intrusion issues; MassDEP and USEPA regulatory interaction; ...

Monte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of Regulatory Affairs. The Associate Director of regulatory Affairs will be responsible for the development and execution of the Regulatory strategy for assigned p...

The Senior Specialist, Regulatory Affairs performs activities to support the regulatory submissions process through development of regulatory strategy and submission of materials to health authorities such as FDA for approval of novel platforms. Support and eventually manage interactions with regula...

Business Analyst will provide business analysis and related duties for various Anti-money laundering (AML) and Compliance Technology projects in the Boston, Massachusetts area. Individual must be able to manage other Business Analyst resources. Manage, coordinate, lead, and set direction of other bu...

The Associate Director, Regulatory Affairs reports to the Senior Director, Regulatory Affairs and executes clinical and preclinical regulatory strategies and activities. Previous experience in representing the sponsor in front of regulatory agencies and as primary regulatory author for regulatory su...

Join Takeda as a Manager, Global Regulatory Affairs CMC Submission Management where you will support the execution of regulatory CMC investigational, registration and post-approval tasks for assigned products. As part of the Regulatory Affairs CMC team, you will report to the Senior Manager GRA CMC ...

The Global Compliance Program Manager helps identify compliance priorities, offers practical and informed solutions, and supports creation and dissemination of best practices for compliance throughout the university worldwide. The Global Compliance Program Manager is the university's primary policy ...

Associate Director, Global Regulatory Affairs in Cambridge, MA with the following requirements:. Master’s degree in Pharmacy, Biomedical Engineering, Regulatory Affairs or related field plus 7 years of related experience. Provide global regulatory oversight and execute regulatory activities on late-...

Associate Director of Regulatory Affairs. Works proactively in a cross-functional organization to partner with various other expertise areas and regional regulatory partners (as applicable) to plan and execute global regulatory filing strategies for company's programs across the portfolio. Provides ...

Program Operations Manager will manage and oversee budgets for the professional graduate programs, initiate a broad range of human resource and faculty personnel actions on behalf of the programs, arrange for purchases, funding transfers, and other fiscal operations for the programs, oversee academi...

Regulatory Affairs Specialist (Medical Device). At least 5 years relevant experience within the regulatory affairs discipline. Work with cross-functional teams consisting of R&D, Quality and Regulatory to gain concurrence on gaps and needed actions to address. Knowledge of EU medical device regu...

As an Associate Director, Global Regulatory Affairs Marketed Products you will define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. Demonstrates acceptable skills with increasing independence ...

L&D (Senior) Program Manager – Onboarding. The L&D (Senior) Program Manager will be instrumental in building a best-in-class team, driving our growth strategy, and fostering a dynamic, innovative culture. Facilitate Keystone’s weekly Orientation program on employees’ day 1, as well as ongoin...

Role: Business Analyst – ISO Compliance. Must have an experience on US Insurance Compliance like- ISO, Regulatory, Statutory Reporting etc. ...