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This includes working with the Rheumatology, Dermatology, and Gastroenterology Brand teams, Co-pay Center of Excellence, MABI, training, BTS, Digital Lab, Medical, Regulatory, Legal, OEC, Public Affairs, Ad Agencies, Media team, and purchasing.
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Assists the Assistant Dean of Student Affairs in determining resource allocation, including budgets and staffing, for student programs, organizations, and events. Essential Duties and Responsibilities: Under the direction of the Assistant Dean for Student Affairs, do the following: A. Guide to Professional Success (GPS) –Scheduling - Oversees and manages GPS CalendarSchedules rooms and appropriate educational technology support for GPS sessions Communication - Manages GPS communication Ensures timely and effective correspondence with session presenters, learning community mentors, and students via email, news board, and student assignments.
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Do you have 3+ years of experience in regulatory affairs, and do you have experience in labeling / preparing safety data sheets? Required Knowledge: Regulatory, Scientific / Technical, QA, Business acumen.
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The Interventional Radiologic Technologist reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.
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Depending on specific role, the Associate Director Regulatory Affairs may be involved in various regulatory activities (oversee activities for regulatory submissions; negotiate with regulatory authorities; oversee processes involved with maintaining annual licenses, registrations, ensure external communications meet regulations; lead crisis management program development and implementation; oversee and manage systems related to product safety issues and product recalls, project management, etc.
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The Data Scientist provides analytical support to Scientific Communications and Medical Affairs HEOR. This position will report to the Director RWE Analytics and provides exceptional opportunities for career development and growth in a cross-functional and cross-regional environment in the pharmaceutical industry.
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Establish team as a critical partner to key internal stakeholders who drive early pipeline strategy including US Commercial Leadership, Asset Strategy Leadership, Pipeline Commercial Strategy Leadership, Medical Affairs/HEOR and International Market Access and Pricing.
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6+ years of progressive medical/scientific affairs experience within the pharmaceutical, biotech industry or at a consulting firm that supports the pharmaceutical or biotech industry; at least 3 years driving medical strategy.
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Certification in RIMS- Certified Risk Management Professional, Regulatory Compliance Manager, Internal Auditor, Public Accountant (CPA) Researches emerging regulatory risks and reports recommendations and observations to senior management.
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Performs imaging procedures in accordance with radiation safety practices as determined by Illinois Dept. of Nuclear Safety and Nuclear Regulatory Commission to limit radiation exposure to patient,self and other healthcare team members.
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The medical director will work closely with Sr. Medical Director and serve as the internal medical/scientific US cross-functional and cross-Alliance (if applicable) point of contact (Global, Clinical Development, Health Outcomes, Scientific Communications, Regulatory, Brand Teams, etc.
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Responsible for talent development for the MMS-PA premarket Regulatory Affairs group; supervises and mentors RA associates. As Manager, Regulatory Affairs, you will provide leadership to the MMS -Pharmacy Automation platform team.
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The position will report directly to the Laboratory Director and work alongside technical staff specialized in fields of analytical, toxicology, and regulatory affairs as well as other labs and functions.
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What you'll be doingThe Medical Science Liaison (MSL) functions as a field-based member of the Medical Affairs group in Medication Delivery, Baxter Healthcare Corporation. This role will collaborate with the internal Commercial and Medical Affairs teams in their therapeutic area of expertise to provide scientific information relevant to the launch of new products, and support key product strategies and publications.
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Partners with Clinical, Regulatory, Operations, Quality, Preclinical Safety, and Commercial organizations. Bachelor's Degree with at least 10 years of experience in a variety of CMC functions required; Master's Degree with at least 8 years of relevant CMC experience required; or PhD with at least 6 years of relevant CMC experience required to effectively manage global teams and all CMC activities with respect to science, technology, quality, regulatory/compliance requirements, budget and resources.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Jobget in Lake Forest, IL
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