Fda Regulations Jobs in Clayton, OH
Fda Regulations Jobs in Clayton, OH

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(The role requires weekly to cover PST time for a couple of days) The Scientific Affairs Manager (SAM) is responsible to inform engage and influence key stakeholders (KSH) at strategic pharma and biotech companies regarding scientific and clinical data supporting Guardant Health More...
Part of Amgens R&D Strategy & Operations organization the R&D Knowledge & Learning team serves staff across R&D and the Office of the Chief Medical Officer transforming how we learn and grow together. We are reimagining learning as an integrated longitudinal journe More...
About The Position The KIPP Foundation is seeking a Senior Director (SD) of Transformation to drive strategic change and innovation across its operations. The SD will be responsible for leading strategic transformation efforts across KIPP Foundation teams (i.e. Finance Scho More...
Job Description: The Patient Services Representative II (PSR II) represents the face of our company to patients who come in both as part of their health routine or for insights into lifedefining health decisions. The PSR II draws quality blood samples from patients and prepares those More...
The VP Copy Market Access is a content leader in the Market Access Strategic Affiliate with oversight of large/mid/small account and complete commercialization agency of record and projects. The VP Copy Market Access is a leadership position that collaborates with all members of the t More...
About This Role Leading and taking full accountability in the successful creation ownership and execution of US Medical Affairs (USMA) operational processes and activities the Sr Manager Medical Affairs Operations Lead (specialty Care) is a critical member of the US Medical Affairs te More...
The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. Has responsibility for 12 of the following: therapeutic area pr More...
The Senior Associate Counsel Clinical Trials and Research provides legal support for clinical trial and research activities across the University of Maryland Medical System (UMMS). This role involves refining processes to streamline timetoactivation for clinical trials standardizing c More...
General SummaryUnder limited supervision is responsible for the collection of the account balances from all third party payors and patients for services rendered at UMMC Kernan and Specialty Hospital. Manages the Cash Posting area and Followup. Develops and maintains the policies and More...
At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...
Vice President Regulatory AffairsHybrid/Remote Options AvailableAre you a strategic leader with a passion for regulatory compliance and higher education Join our team as Vice President of Regulatory Affairs where you will shape compliance strategies build key regulatory relationships More...
About This Role The Associate Director Statistical Programming will be reporting to the Statistical Programming & Clinical Data Sciences Lead for Biogens West Coast Hub. He/She will lead and oversee statistical programming activities of internally and externally through vendors en More...
About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri More...
Job Title: Validation Engineer III Location: Santa Monica CA Duration: 06 months contract with possible extension Shift Details: 1st Shift/ MF 85 Pacific/ Onsite at least 3 days a week (Hybrid) Pay Range: $60$80/hr w2 Position Details: Responsible for developing CSV related docu More...
At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...
About the Role:We are seeking a highly experienced and visionary Senior Manager for our AI Foundation team. This role is pivotal in driving the strategy development and implementation of AI capabilities services and solutions to assist our organizations AI initiatives that is a mix of More...
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