- Interpret regulatory filings and lead cross-functional teams to comply with new or revised regulations.
- Cultivate relationships within Customer Operations, throughout the Company and with external stakeholders. Partner with Corporate Affairs, Rate Engineering, Law, Customer Energy Solutions, Corporate Accounting and IT, and other organizations as needed.
- Track Customer Operations' compliance with rate case and other regulatory requirements including development and management of project plans and executive updates.
- Maintain well organized files and accurate records including maintaining back-up for reports and computer files, and safeguarding computer facilities, reports, and work papers.
- 5 years' experience as a project manager in a regulated industry
- Demonstrated ability to be well organized, detail oriented, and flexible to handle multiple assignments and deadlines.
- Must have the ability to interact and partner with various levels of management and internal/external organizations. Required
- Must have experience handling multiple assignments and changing priorities. Required
- Must have experience working independently and making sound business decisions. Required
- Must have demonstrate excellent oral communication skills and strong leadership skills. Required
- Proficient in Word, Excel and PowerPoint. Required
- Experience in project management. Required
- Regulatory experience. Required.
- Regulatory or energy industry experience required. Preferred
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Regulatory Affairs Specialist
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Thrive Boston, United StatesA clinical-stage bio pharmaceutical client whose mission is to develop new therapies for people with rare diseases is looking for a Regulatory Affairs Specialist with pharmaceutical and/or biotechnology experience · The Regulatory Affairs Manager will support regulatory activiti ...
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Sr. Regulatory Affairs Specialist
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Hyperfine Boston, United StatesCompany Profile · Hyperfine (NASDAQ: HYPR) is the groundbreaking MedTech company that created Swoop, the world's first FDA-cleared portable magnetic resonance imaging (MRI) system capable of providing neuroimaging at the point of care. Our mission is to transform patient care by ...
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Principal Regulatory Affairs Specialist
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Thrive Boston, United StatesA clinical-stage bio pharmaceutical client whose mission is to develop new therapies for people with rare diseases is looking for a · Regulatory Affairs Specialist · with pharmaceutical and/or biotechnology experience · The Regulatory Affairs Manager will support regulatory ac ...
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Expedited Specialist II, Human Research Affairs
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Partners Healthcare System Boston, United StatesCome join our team and play a pivotal role in promoting and ensuring an environment where human subject research is conducted according to the highest standards · Our Team · Our Human Research Affairs Compliance and Education Office was established in June 1999 as the Quality Ass ...
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Mantell Associates Boston, United StatesMantell Associates is currently partnered with an innovative Biotech company, developing much-needed therapies for people with solid tumors/lung cancer and rare endocrine diseases, who are searching for a Director / Senior Director of Regulatory Affairs. · Director of Regulatory ...
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Medtronic plc Boston, United States1325 open jobs. · Use your resume to get matched with the right job. · or Build your resume · Senior Director, Regulatory Affairs, Robotics · Boston, Massachusetts, United States and 2 more · Regulatory Affairs · Senior/Principal Robotic Surgery Start-Up Specialist · Oslo, Oslo ...
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Regulatory Documentation Specialist
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Digital Prospectors Boston, United StatesPosition: Regulatory Documentation Specialist · Location: Boston, MA (Onsite) · Length: 6+ months · Job Description: · Our client is seeking a Regulatory Documentation Specialist who will be responsible for overseeing, organizing, and preparing regulatory documentation essent ...
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Associate Director, P&R
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Faculty Affairs Coordinator
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