Regulatory jobs in Dover, DE

What Regulatory Affairs contributes to Cardinal HealthRegulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing...

Overview Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed...

A leading global information services provider in Dover, DE is seeking a Senior Field Sales Executive. This role demands expertise in regulatory compliance and sales acumen to support the sales team and engage with clients effectively. Candidates should have a Bachelor's degree, at least 5 years of experience, and a proven ability to analyze market opportunities. The position offers competitive...

Job DescriptionOracle Health Data Intelligence (HDI) is building the next generation of intelligent, cloud-based healthcare platforms - combining clinical, payer, and regulatory data at scale to transform how care is delivered and measured. We are bringing hyperscaler technology to healthcare, integrating advanced AI, secure data exchange, and regulatory-compliant infrastructure to accelerate...

Regulatory Reporting Senior Associate, Controllership - RemoteCountry: United States of America It Starts Here: Santander is a global leader and innovator in the financial services industry and is evolving from a high-impact brand into a technology-driven organization. Our people are at the heart of this journey and together, we are driving a customer-centric transformation that values bold...

Quivvy Tech is currently hiring telemedicine physicians!Quivvy Tech is the fastest growing national telemedicine network in the U.We have a triage call center where all patients are pre-screened for medical necessity and to confirm compliance with legal and regulatory standards all while ensuring a positive patient experience.Telemedicine Physician Responsibilities Include: Evaluate patients...

A leading pharmaceutical company is seeking an Associate Director of Regulatory Intelligence to oversee the collection and dissemination of regulatory insights. This role requires managing a team, directing communications and ensuring access to crucial regulatory information. Candidates should have a Master’s degree and extensive experience in regulatory affairs, with strong leadership and...

A leading global pharmaceutical company is seeking an Associate Director of Regulatory Affairs in Dover, Delaware. This role involves managing regulatory submissions and providing strategic regulatory input for oncology products. Ideal candidates should have a bachelor's degree, substantial experience in the biopharmaceutical industry, and specific experience in regulatory affairs. The position...

Job DescriptionOverviewWe are seeking a highly experienced sales and business development professional to drive growth across Commercial, Real-World Evidence (RWE), Clinical, Regulatory, and Safety research services within pharmaceutical and biotechnology organizations. This role is responsible for identifying, developing, and closing complex, large-scale engagements by aligning client needs with...

Job DescriptionAssists and supports the organization in complying with, as well as the ongoing preparation, testing and monitoring of conformance to, the requirements of government regulations and/or regulatory agencies.Responsibilities+ Performs evaluation of internal operations, controls, communications, risk assessments and maintenance of documentation as related to regulatory compliance and...

A global pharmaceutical company is seeking a Vice President of Regulatory Affairs Oncology in Dover, Delaware. This leader will drive regulatory strategy for oncology therapies, leveraging over 15 years of biopharmaceutical experience. Key responsibilities include managing regulatory submissions and ensuring compliance with FDA regulations. The ideal candidate will hold an advanced degree and...

Overview Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.). The company focuses on oncology, urology, women's health, rare diseases, cell & gene therapies and CNS with a diverse pipeline. For more information on SMPA, visit our website or follow us on LinkedIn. Job Overview We are seeking a dynamic, highly...

Job DescriptionAbout the Role:At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large, complex global health companies requires regulatory leaders who are deeply steeped in the public and private levers that impact this industry. To remain competitive in this rapidly changing landscape, organizations...

Job DescriptionOracle Health Data Intelligence (HDI) is hiring a Principal Technical Program Manager - Operations to lead key strategic and operational initiatives across the organization. This is a highly visible role where you'll report directly to the Director of Operations as a right-hand leader and help scale programs, headcount, tooling, and processes across operations, engineering,...

Job DescriptionAbout the RoleOracle Health Data Intelligence is entering a high-impact phase of MDR (Medical Device Regulation) readiness and regulatory transformation . Over the next year, HDI must execute a large volume of technical documentation, risk management activities, and engineering design updates required for compliance across our AI-enabled population health platform.To support these...

Job DescriptionOracle Health is a comprehensive suite of healthcare technology solutions designed to help organizations advance patient care, improve operational efficiency, and enhance caregiver experiences. Building on Oracle's global expertise in cloud technology, data management, and analytics, Oracle Health delivers integrated electronic health records (EHR), population health tools, and...

Job DescriptionManages the ongoing preparation, testing, and monitoring of compliance with information security standards and government regulations and regulatory agencies as it relates to the design, development, and deployment of products and services. Key Responsibilities:+ Lead, mentor, and grow a team of compliance and security specialists.+ Manage customer engagements focused on compliance...

Job DescriptionAbout the RoleOracle Health Data Intelligence is entering a high-impact phase of MDR (Medical Device Regulation) readiness and regulatory transformation . Over the next year, HDI must execute a large volume of technical documentation, risk management activities, and engineering design updates required for compliance across our AI-enabled population health platform.To support these...

Job DescriptionModern healthcare demands integrated solutions. At Oracle Health, we connect patients, providers, payers, and public health organizations with AI-powered, interoperable solutions that help streamline data exchange, surface actionable insights, and drive operational efficiencies across the care continuum.As an Interoperability Regulatory Strategist, you will monitor and evaluate...

Job DescriptionAbout the RoleOracle Health Data Intelligence is entering a high-impact phase of MDR (Medical Device Regulation) readiness and regulatory transformation . Over the next year, HDI must execute a large volume of technical documentation, risk management activities, and engineering design updates required for compliance across our AI-enabled population health platform.To support these...