Regulatory Coordinator: Average Salary in Massachusetts in 2024

Regulatory Project Coordinator 2044984. ...

Senior Clinical Research Regulatory Coordinator, Center for Clinical Investigation, Hybrid-(3302525). The Senior Research Regulatory Coordinator (RC) works under the direction of the CCI Executive Director, Research. Operations Director and Principal Investigator(s) to complete the regulatory requir...

Are you a regulatory project coordinator who takes pride in seeing programs move into the clinics and through to commercialization?. ...

The Regulatory Coordinator will contribute to the regulatory/ethics/IRB submission consultations process, ongoing educational initiatives, and Research Professionals Network (RPN) of the Clinical Research Resources Office (CRRO) at Boston University Medical Campus. REGULATORY COORDINATOR, School of ...

The Clinical Research Regulatory Coordinator I (CRRCI) works under general supervision to ensure the regulatory requirements for clinical trials are met. Clinical Research Regulatory Coordinator---Cancer Center Protocol Office-(3302823). The Cancer Center Protocol Office is seeking motivated, detail...

Regulatory Contracts Coordinator/Specialist 2044987. This position is responsible for overseeing the regulatory contract process, from negotiating agreements and vendor setup to ensuring compliance and handling all related documentation. ...

Senior Clinical Research Regulatory Coordinator, Center for Clinical Investigation, Hybrid-(3302525). The Senior Research Regulatory Coordinator (RC) works under the direction of the CCI Executive Director, Research. Operations Director and Principal Investigator(s) to complete the regulatory requir...

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The Regulatory Coordinator will contribute to the regulatory/ethics/IRB submission consultations process, ongoing educational initiatives, and Research Professionals Network (RPN) of the Clinical Research Resources Office (CRRO) at Boston University Medical Campus. The Regulatory Coordinator will pe...

The Regulatory Affairs Coordinator (RAC) will work with investigators, sponsors, Institutional Review Boards (IRB) and research support staff to ensure that regulatory requirements are met for clinical trials. Regulatory Affairs Coordinator - Cancer Center Protocol Office-(3302443). This role report...

The Project Coordinator will support teams of investigators, biostatisticians, and project managers in preparing proposals and conducting projects. Oversee logistics of research projects, and participate in the cycle of grant application and renewal processes for projects and work closely with the f...

The Compliance Analyst will be a member of the Legal, Compliance & Risk Group and will report to the WFD Compliance Officer. Compliance analyst, client platform Compliance. The Sales and Marketing Compliance Analyst will support Wellington Management's sales and marketing compliance program, with a ...

As CAISO Program Manager, you will have responsibilities to build, execute, and measure performance of Stem's market operations in North American wholesale electricity markets. This effort includes developing, implementing, and monitoring program operations strategies, project planning, portfolio an...

The Principal Regulatory Specialist is responsible for carrying out Pre-Market and Post-Market regulatory activities in compliance with Digital Factory's Quality Management System for domestic and various international markets for SaMD products. Conceive of and Implement the Regulatory Strategy in ...

Technical Project Managerwill report to and work closely with the Director, Digital LIMS Systems to ensure the implementation of new solutions and improvement of existing systems (LabVantage) for the Moderna Digital Laboratory Systems organization. Act as the Technical Project Manager for the LabVan...

Serve as a CMC strategist and project leader for projects/programs, providing regulatory assessments and developing regulatory strategies with input from the Executive Director Regulatory Affairs CMC. The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for exe...

We are seeking a highly motivated and experienced Associate, Benefits and HR Compliance, (Compensation experience a+) to join our dynamic organization. The ideal candidate will have a strong background in benefits administration, data analysis, and compliance management, with specific experience in ...

Join Takeda as an Associate Director, Global Regulatory Affairs CMC where you will develop and lead the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products. Can apply and adapt this understanding to projects to enhance probability of regula...

Under the direction of the Senior Director, Accreditation & Regulatory and working collaboratively, the Accreditation and Regulatory Specialist (Nurse) leads efforts to ensure continual organizational compliance and ongoing readiness with clinical quality and patient safety standards and regulations...

Program Coordinator- Adult Behavioral Health Unit. Oversees the day to day operations of the Group Therapy Program and supervises other clinicians who lead groups. ...

As our Senior Compliance Analyst, you will report to our Senior Compliance Leader, who reports to our Group Benefits Senior Compliance Lead. Support the implementation of enterprise compliance projects and initiatives including compliance risk assessments and compliance trainings. We drive a high-pe...

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...

Previous experience of Agile Program management (e. Experience of a wide range of Technology roles is desirable, ideally with some form of development engineering or Agile Program management background. Prior experience working with an OCIO investment manager involving a mix of traditional and alter...

The Human Research Compliance Specialist (compliance auditor) provides education and support to researchers and is responsible for performing audits of IRB-approved clinical research protocols across our institutions to ensure compliance with FDA, OHRP and other state and government regulations, Goo...

The Business Control Manager - Preferred Project Execution is a member of the Consumer Investments (CI) Supervision Leadership Team and reports to several different stakeholders potentially including other Division Supervision Managers (I and II) and the Complex Products & Platform Supervision l...