Clinical Training Specialist (Clinical Science Liaison – CSL) Albany/Rochester, NY Siemens HealthineersClinical Training Specialist (Clinical Science Liaison – CSL) Albany/Rochester, NYWashingtonRemoteExport Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”. Varian Medical Systems, a Siemens Healthineers company is hiring a Clinical Training Specialist (CSL) for the Albany/Rochester, NY area supporting Varian Interventional Solutions (VIS) by providing in‑person case coverage, clinical education, and first-line technical support for VIS products.
Radiochemist GuidehouseRadiochemistBethesda, Maryland$74,000–$124,000 / yearProduce tracers to support preclinical and clinical research and transition promising radiotracers from research-scale synthesis to GMP-compliant production when appropriate. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.
Associate Director, Digital Health Business Development IQVIAAssociate Director, Digital Health Business DevelopmentWashington, District of ColumbiaThis individual will serve as a trusted advisor to MedTech, software, and healthcare technology organizations, helping clients navigate complex challenges related to connected devices, Software as a Medical Device (SaMD), cybersecurity, human factors engineering, regulatory compliance, clinical evidence generation, and commercialization. Identify and close opportunities related to Digital Health Technologies, Software as a Medical Device (SaMD), Artificial Intelligence/Machine Learning-enabled devices, Human Factors Engineering and Usability Validation, Medical Device Cybersecurity, and Clinical Evaluation and Evidence Generation.
Director, Regulatory Affairs – Regenerative Medicine & Biologics Quality IQVIADirector, Regulatory Affairs – Regenerative Medicine & Biologics QualityWashington, District of ColumbiaExperience: Minimum five years of experience in Regulatory Affairs related to FDA oversight of various human medical products (HCT/Ps, drugs and/or biologics, medical devices, and combination products)developing regulatory deliverables and submissions. The primary roles and responsibilities include managing the development of regulatory submissions, development of overall regulatory strategy, communicating with regulatory bodies and clients, and leading or expanding new therapy ideas, as applicable.