- Sallie Mae (New Castle, DE)
- …generations, for the future of education. **What You'll Contribute:** The Associate , Education will be responsible for designing, delivering and evaluating ... will design, deliver, and continuously improve training programs aligned with regulatory requirements, contact center KPIs, and customer experience standards. **What… more
- Sallie Mae (Newark, DE)
- …highly regulated industry is strongly preferred, including familiarity with bank regulatory frameworks relevant to contracting principles. + Experience advising on ... intellectual property and technology transactions, as part of an IP transactional or technology transactions practice at a law firm or in a sophisticated in-house environment. + Experience in various forms of corporate transactions, including but not limited… more
- GRAIL (Dover, DE)
- …For more information, please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership with key internal ... including Multi-Cancer Early Detection (MCED). The position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements,… more
- Terumo Medical Corporation (Elkton, MD)
- …Primary responsibilities of this position include environmental permitting and regulatory compliance, as well as planning, developing, implementing and administering ... identifying, recommending, and driving improvements. 7. Identify and interpret EHS regulatory standards that impact operational exposures and business activities and… more
- Terumo Medical Corporation (Elkton, MD)
- …or Microbiology Manager, accordingly. **Job Details:** 1. General Requirements: 1. Associate is responsible for following requirements of applicable national and ... knowledge of Terumo Safety Policies and Procedures to assure compliance with regulatory , global and site quality requirements. 3. Can work independently, with… more
- Parexel (Dover, DE)
- …for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at ... in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and… more
- Parexel (Dover, DE)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local ... in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and… more
- Parexel (Dover, DE)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... command of process details + Demonstrated knowledge of global and local regulatory requirements + Demonstrated understanding of key operational elements of clinical… more
- ABBTECH Professional Resources, Inc. (Dover, DE)
- **Financial Project Associate ** **Exempt** Embark on a dynamic career with Premier Group Services, Inc., a leading CPA Management and Consulting firm dedicated to ... approach that ensures responsiveness and lasting relationships. **Join as a Project Associate ** As a Project associate at Premier Group Services, Inc.,… more
- Parexel (Dover, DE)
- …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...including medical review of serious adverse events. - Support regulatory safety reporting activities - Ensure client needs and… more
- CSL Behring (King Of Prussia, PA)
- …therapies that make a meaningful difference worldwide. We are looking for a ** Associate Director,** **Case Management Intake & Submissions** to join our R&D team. ... monitor successful reporting and resolve submission failures to minimize impact to regulatory compliance. The Case Submission aspect of the function has a high… more
- CSL Behring (King Of Prussia, PA)
- …developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, PV Standards and Governance? The job is in our King of ... and quality in safety data management across the R&D organization, supporting regulatory readiness and scientific integrity. **The Role** + Maintain PV data… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical ... strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables...study design and data analysis for clinical trials and regulatory submissions + Influence and contribute to clinical development… more
- Parexel (Dover, DE)
- …readiness for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation of FSFV + ... with CRA for enrollment delivery during study conduct + Partners with local Regulatory authorities and Study Start up teams to ensure timely completion on country… more
- CSL Behring (King Of Prussia, PA)
- Associate Director, Corporate & External Affairs, R&D Portfolio **Position Purpose:** The Associate Director, Corporate and External Affairs, R&D Portfolio will ... for patients and partners. + Serve as a key partner to regulatory policy team providing strategic counsel on advocacy opportunities, and stakeholder engagement.… more
- CSL Behring (King Of Prussia, PA)
- **Job Title:** Associate Director, Strategic Forecasting and Portfolio Analytics **Reporting to:** Director, Strategic Forecasting & Portfolio Analytics **Position ... scenario modeling; forecast submission - Stay updated on industry trends, regulatory changes, and advancements in forecasting methodologies within the biotech and… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director, Commercial Data Science & AI is crucial in driving the overall strategy for (Gen)AI tools and technologies within CSL. This individual will ... decisions + A deep understanding of the pharmaceutical industry, including regulatory requirements, market dynamics, and emerging AI technologies, with the foresight… more
- Parexel (Dover, DE)
- …to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator ... document structure, content, and style adheres to FDA/EMA or other appropriate regulatory guidelines, and comply with departmental, corporate or client SOPs and… more
- CSL Behring (King Of Prussia, PA)
- …trackers, SOPs, and governance frameworks that ensure scientific integrity and regulatory compliance. You will also drive innovation in publication metrics and ... digital engagement, helping us measure and enhance our scientific impact globally. As a more senior member of the publications team, you will also be expected to provide strategic and operational mentorship to less experienced colleagues. **RESPONSIBILITIES… more
- CSL Behring (King Of Prussia, PA)
- …of biotech/pharmaceutical experience. **Experience** + Strong knowledge of the regulatory requirements for MDRP, Medicare/IRA, Veteran's Healthcare Act, and other ... Federal regulations mandating price and/or transparency disclosures. + Experience with implementation and utilization of financial & pricing systems. Model N preferred. + Strong Excel skills as well as MS Office proficiency Demonstrated ability to function… more
