- Takeda Pharmaceuticals (Raleigh, NC)
- …Director , GRO Regulatory Project Management and be a part of the Global Regulatory Affairs Team. **How you will contribute:** + As Associate Director , ... process changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global Regulatory Project… more
- Veterans Affairs, Veterans Health Administration (Durham, NC)
- …training, implementation of local and national policies, Directives, and Regulatory Requirements pertaining to disruptive behavior. Clinical Duties: 1. The ... program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus...programs were sanctioned by the VHA Central Office Program Director for Psychology and the VHA Office of Academic… more
- J&J Family of Companies (Raleigh, NC)
- …partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs , clinical pharmacology, health economics, and the disease ... Medical Director / Sr. Med Director , Clinical Research...compound through close partnership with the compound global medical affairs leader. + Serves as the clinical leader for… more
- Takeda Pharmaceuticals (Raleigh, NC)
- …You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met ... therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible...+ Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts… more
- Gilead Sciences, Inc. (Raleigh, NC)
- …to help transform innovations to life-changing medicines for patients. The Senior Director , RWE Innovation Methods and External Partnerships reports to the Executive ... Director , RWE Generation and is accountable for the development...as an in depth understanding of the pharmaceutical industry, regulatory strategy and evidence generation. **What will you be… more
- Takeda Pharmaceuticals (Raleigh, NC)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …Type: Permanent Staff (EHRA NF) Vacancy ID: NF0008195 Position Summary/Description: The Director of Revenue Cycle reports to the Associate Dean of Finance and ... ) office and will work closely and in partnership with the Clinical Affairs team. Centralized functions include: Payor Contracting and Evaluation, Regulatory … more
- Sumitomo Pharma (Raleigh, NC)
- …impacting business decisions. + Proficient in GMP manufacturing, quality assurance, regulatory affairs , and clinical operations. + Demonstrated ability to ... **Executive Director , Commercial Supply Chain** Sumitomo Pharma America (SMPA)...of all products. + Identify risks (business, performance, quality, regulatory , external, etc.) to ensure supply and work with… more
- ThermoFisher Scientific (Morrisville, NC)
- …regulatory agencies. + Requires strategic business partnering with Medical Affairs , Regulatory , Clinical Operations, Project Management, Patient Advisory ... cancer. **How will you make an impact?** The **Sr. Director , Procurement - Clinical Research Group (CRG)** is the...the required onboarding due diligence and continuous assessment of regulatory , compliance, and risk for suppliers used for global… more
- The Clorox Company (Durham, NC)
- …across our BU's through strong working relationships with leaders in R&D, regulatory , manufacturing, commercial, government affairs and sustainability. + Foster ... you will work within a team of product safety, chemical management, and regulatory professionals in R&D's Global Stewardship (GS) department to build our Product… more
- Institute for Medical Research (Durham, NC)
- …and facilitating resource sharing amongst teams. The position will report to the Director or their designee and may supervise mid-level managers and other study ... software Critical Element 2 - Supervise Clinical Research Coordinators, Regulatory Coordinators, Project Scientists, and/or Business Administration personnel: +… more
- Prime Therapeutics (Raleigh, NC)
- …determinations with requesting physicians or ordering providers, when available, within the regulatory time frame of the request by phone or fax. + Provides ... training per inter-rater reliability process. + Assists the VP, Medical Affairs in research activities/questions related to the Utilization Management process,… more
- Merck (Raleigh, NC)
- …partnership with GCTO (Global Clinical Trial Operations) country operations, finance, regulatory affairs , pharmacovigilance, legal and regional operations, HQ ... appropriately in a timely manner. + Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out. +… more
- Institute for Medical Research (Durham, NC)
- …Human Resources on trends, underlying risks, and recommendations + Assist the HR Director in the completion of government, regulatory , and compliance reporting + ... is under the direct supervision of the Human Resources Director . The prior statements describe the general nature and...programs may be required for all Department of Veterans Affairs Health Care Workers Without Compensation (WOC) appointments. We… more
- Merck (Raleigh, NC)
- …as needed different challenges and issues to TA Head/CRD Clinical Research Director /CCQM Country Clinical Quality Manager and or CTT Clinical Trial Team (as ... regional and local operations, EU Clinical Development, Pharmacovigilence, Global Medical Affairs to align on key issues/decisions across the trials. Consult with… more