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Work closely with the Head of Regulatory Affairs to ensure our research is designed to meet stringent FDA regulatory standards for safety and efficacy. Quality Assurance & Regulatory Affairs Integration: Work closely with the quality assurance and regulatory affairs teams to embed scientific excellence into every aspect of product development and compliance.
$250,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Collaborate closely with Preclinical, Clinical, Regulatory Affairs and Medical Affairs to ensure efficient and robust strategic integration of drug safety plans. Experience working with the a global safety database, medical coding (medDRA and WHO) and other data systems in clinical setting.
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Collaborate with cross-functional teams, including analytical development, formulation development, quality assurance, and regulatory affairs, to ensure seamless project progression. Collaborate with regulatory affairs to support regulatory submissions and inspections.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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About the Role:Join our compassionate Kia Care Consumer Affairs team as a Remote Total Case Specialist. This includes: an industry-leading dispatch management platform powered by Swoop; comprehensive accident management services; knowledgeable consumer affairs and connected vehicle capabilities; and a growing marketplace of services, discounts and support enabled by a robust partner ecosystem.
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The Director/Senior Director, Intellectual Property will work closely with research and development, business development and external patent counsel to lead and implement our intellectual property (IP) affairs, including the overarching strategies for our portfolio of clinical stage assets.
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Lead activities establishing a top-tier Regulatory Affairs department, including the development of policies and procedures aligned with GxPs, Guidance, and best practices. Reporting to the Senior Vice President, Regulatory Affairs, the successful candidate will support the development of comprehensive regulatory strategies and collaborate with cross-functional teams to efficiently develop products in accordance with global regulations and guidelines.
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This individual provides oversight and assistance to Medical Affairs, internal partners, and external vendors to ensure completion of scientific communications projects in an efficient and timely manner that are medically and scientifically accurate and of high editorial quality.
$233,960 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Under the general direction of the MassHealth Chief Medical Officer, or designee, the Program Manager for MassHealth Health Equity Programs works directly with MassHealth Program and Office of Clinical Affairs leadership to manage health equity measurement and value-based care initiatives for MassHealth programs.
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As a Senior Regulatory Affairs Specialist at Verily, you will work closely with other Regulatory Affairs team members, experts from diverse fields (e.g., Biology, Chemistry, Physics, Electrical Engineering, Computer Science) to develop, manage and execute regulatory strategies to obtain market clearances for innovative products.
$166,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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College degree or equivalent in any relevant field such as security studies, law enforcement, intelligence, political science, international affairs; advanced degree is not required. Provide direct support for regional security operations, event security, executive protection and intelligence needs.
$108,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Represent PCDS at team meetings and coordinate between PCDS and other functions including CMC, Regulatory Affairs, Clinical Operations, and Platform and Discovery Sciences. Design toxicity studies: coordinate with Preclinical Outsourcing for placement and monitoring of the studies as well as the Bioanalytical and DMPK groups regarding integration of bioanalysis and toxicokinetic aspects into these studies to ensure on-time delivery of key data and study reports.
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They collaborate with faculty, the HMS Dean for Clinical and Academic Affairs, and others in the HMS Dean’s Office to achieve these objectives in supporting gender equity and positive faculty experience through development and implementation of programming that includes a focus on community building, mentoring and leadership training, and promoting the visibility and interests of women in science.
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Those interested in the role should address a letter of interest and CV to:Dr. Paul Alfille, MGH Anesthesia Vice Chair for Clinical Affairs Dr. Doug Shook, BWH Anesthesiology Deputy Chair )with cc to: Danielle Le Hals, MGB Enterprise Vice President of Anesthesiology class="blockpanel">.
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JOB GOALS: The Director of Finance for the Arlington School Department has responsibility for supporting the Assistant Superintendent for Finance & Operations with administering and supervising the business affairs of the district; ensures all duties and responsibilities associated with purchase order processing, accounts payable, accounts receivable, state reporting, student activity funds, grants, revolving funds, etc.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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The Associate Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (HCP’s, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities.
Full-timeExpandApply NowActive JobUpdated 14 days ago
affairs job Title: assistant Company: Citi in Watertown, MA
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