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Key Skills: ISDA, Derivatives, law degree preferred, legal trade documentations, Credit risk. Responsible for complete documentation process from drafting, reviewing and negotiating to execution & filing of the CDEA, ISDA/CSA, ancillary documents such as novation and related regulatory initial margin documents.
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Qualifications: Bachelor's degree in Speech-Language Pathology or related field. Valid SLPA certification or license (if required by state). Minimum 1+ years speech therapy experience required.
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Develop, implement, and monitor procedures designed to promote compliance with IACUC policies and procedures and integration with other committees, such as the Institutional Review Board (IRB), Institutional Biosafety Committee (IBC), Chemical Safety Committee (CSC), and offices, such as the Sponsored Programs Administration (SPA), Office of Technology Development, and Legal Affairs.
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We’re a leader in staffing Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, HEOR, Market Access, and Sales & Marketing roles. Medical Science Liaison, Medical Device, Respiratory (Central) TMAC - Dallas, TX, United States Tagged: TMAC Direct Hire, Pharmaceutical, Medical Science Liaison, Respiratory, Field Medical , TMAC, Medical Affairs, MSL Medical Science Liaison, Medical Device, RespiratoryTwo Territories: Central and WestTMAC’s direct-hire service, formerly known as TMAC Direct, is an executive search firm and Pharma’s Complete Recruiting Resource.
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Qualifications for virtual production studio manager (Required and Desired) Bachelor’s degree in audio/visual communications, design, production or journalism communications and four years’ related experience, or equivalent combination of education and experience.
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There is NO experience required, paid training is provided for all job openings. To qualify for employment, you must be 18 years of age or older, have a high school diploma or a GED (NO college required) and be a U.S. citizen (or have a Green card.
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Certified Regulatory Compliance Manager (CRCM), Certified Securities Compliance Professional (CSCP), or other relevant compliance certifications. Bachelor's degree in finance, business administration, legal studies, or a related field; advanced degree or relevant certifications preferred.
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Juris Doctor (JD) degree. Bachelor’s or advanced degree in Electrical Engineering, Computer Engineer, Physics, Chemical Engineering, Materials Scienceor related field. TI’s legal department is seeking a talented Patent Attorney with a background in semiconductor engineering within the Embedded Processors, Device Manufacturing, and Analog Design space.
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Completion of a graduate level degree (PharmD, MD, DO, DNP, PhD, MSN, MS or equivalent healthcare professional degree) along with relevant clinical experience. Provide field-based medical affairs assistance for clinical research initiatives supported by Company, related to Investigator Initiated trials, or collaborative initiatives.
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Contribute to the preparation and review of CMC (Chemistry, Manufacturing, and Controls) documentation, particularly focusing on the analytical sections required for regulatory filings(BLA/MAA), including post-approval submissions to US and EU regulatory bodies.
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Your JobThe Product Safety & Regulatory Compliance Team is seeking a Regulatory Affairs Manager to join our team. Who You Are (Basic Qualifications)Experience working in regulatory compliance, chemical control, regulatory affairs, environmental, laboratory or product safety in the agriculture industry Experience working with chemical regulations Experience in the agricultural products / fertilizer industry.
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Prior experience in compliance, product controllers, legal, regulatory, audit or risk management functions in the firm's various businesses, e.g., consumer banking, asset or wealth management and/or global banking and markets businesses.
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Required: Law degree from accredited school. Required: Bachelor's Degree. This role collaborates with Legal Department colleagues on legal and regulatory issues related to technology contracts, emphasizing privacy, security , and regulatory compliance.
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Experience in other Medical Affairs functions (i.e., Publication Planning, Scientific communications, HEOR, etc.) Inizio Engage has a strong partnership with an emerging biopharmaceutical company in endocrinology/rare disease to support Medical Affairs activities and execution.
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And 3 years Required or Master Degree in Geotechnical Engineering or related degree from an ABET accredited program and 2 years Required Basic knowledge in standard geotechnical engineering techniques, principles and procedures.
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regulatory affairs degree required jobs in Dallas, AZ, United Kingdom
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