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Reporting to the Head of Process and Analytical Development – Cell Therapy, the Director of Analytical Development will be accountable for the flawless execution of the Cell Therapy Analytical Development activities (internal and client-focused); spanning technical development, method transfer, manufacturing, product release and successful preparation of regulatory submissions.
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Reporting RelationshipTypically Director or aboveSkills, Knowledge & AbilitiesExpert knowledge of the professional services industry, ideally Lawyers Professional Liability claims, policy language, coverage, and claim practices.
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As a Technical Support Engineer Intern, you will be responsible for:You will assist and answer inquiries within businesshours and within SLAs. You communicate clearly and effectively. Thencome and join our global team as a part time Technical Support EngineerIntern.
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Directly investigate each claim through prompt and strategically-appropriate contact with appropriate parties such as policyholders, accounts, claimants, law enforcement agencies, witnesses, agents, medical providers and technical experts to determine the extent of liability, damages, and contribution potential.
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Working closely with the SVP / Senior Director of the VMO & PMO, the Director of Third Party Monitoring will be responsible for the development and implementation of a robust continuous monitoring function for our third and Nth-party relationships.
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Your primary responsibilities as Medical Director include upholding medical quality standards (patient care, client and referral veterinarian satisfaction, and patient safety), supporting quality and operational initiatives, fostering a clinician-driven culture and one that cultivates a learning environment, and clinician recruiting, engagement, and retention.
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In conjunction with the Vice President of Operations, the Area Director is responsible for overseeing management, customer service and operations at those facilities under his/her auspices to ensure adherence to policies and procedures and professional standards as established by AdvantageCare.
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Senior/Executive Director, Clinical Pharmacology We are seeking a highly skilled and motivated Clinical Pharmacologist with a background in pharmacokinetic modeling to join our dynamic research and development team.
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Could you be our next Senior Director of Clinical Research and Development? CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. Knowledge of the drug development process and clinical research methodologies including experience in clinical trial design, data analysis/statistics and data interpretation; knowledge of regulations, ICH/GCP, adverse event management.
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We are seeking an experienced Senior Counsel at the Director level to join our legal team. Juris Doctor (JD) degree from an accredited law school. This role requires a diverse skill set across clinical operations/development and contracts/legal operations.
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The National Director, Field Medical Affairs (FMA) will be responsible for providing leadership, oversight, and overall direction to the Medical Science Liaison (MSL) and Clinical Device Liaison (CDL) teams.
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The Sr Director of GSK Market Access Strategy, Anti-Infective (AI) Vaccine (Vx) & Launch Excellence (LE) is a highly visible position within GSK US Market Access as well as the AI & Vx Business Units, reporting to the head of the US Market Access Strategy team.
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Aramark Healthcare+ is seeking candidates for an Environmental Services Director position at Riddle Hospital located in Media, PA. This is a management position, responsible for developing and executing custodial solutions to meet customer needs.
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You will be responsible for all CSL Group entities in the Americas including Behring and Seqirus.
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The Senior Associate Director oversees technical systems used by Advancement and develops through software programming knowledge reporting and data visualization for Advancement staff, College leadership, and College volunteers.
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Title: character technical director Company: Genies in Villanova, PA
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