- Northeast Georgia Health System, Inc (Gainesville, GA)
- …a foundation of improving the health of our communities. About the Role:Job SummaryThe Research Regulatory Specialist performs a wide range of tasks ... essential to the submission, approval, and maintenance of required regulatory documents for conducting clinical research in...of required regulatory documents for conducting clinical research in compliance with the Federal Food and Drug… more
- Merck & Co. (Rahway, NJ)
- …products and interests from the world's biomedical literature in support of regulatory , clinical research , marketing, and legal functions.- Plans, organizes, ... Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's… more
- Merck & Co. (Rahway, NJ)
- …dedicated colleagues while developing and expanding your career.The Senior Trial Initiation Specialist in Global Site Budgets and Payments will be responsible for ... Minimum of three (3) years of relevant experience in clinical research setting.Business acumen and/ or financial background; preferably Investigator grants and… more
- Merck & Co. (Rahway, NJ)
- …CCDS, CCPPI, CCIFU) and US labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of the EU Labeling and other ... and implementing US Labeling for assigned products in line with regulatory requirements and internal standards and guidelines.- Assisting with developing and… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must actively support, participate and embrace an empowered team culture… more
- Merck & Co. (Millsboro, DE)
- …tests, and review and release of antigen and seed batches. The QC associate specialist must adhere to regulatory and site policies and procedures governing the ... with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract… more
- Merck & Co. (North Wales, PA)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... data governance reviewsThe Global Clinical Data Standards (GCDS) Data Standards Specialist may contribute to the definition and maintenance of business processes… more
- Merck & Co. (Durham, NC)
- …Durham employs 1,000+ people. This role as a Training Operations Associate Specialist will be an energetic individual with strong interpersonal, leadership, and ... manufacturing and related systems (ie SAP) Familiarity with pharmaceutical regulatory requirements Project management and data analysis skillsTechnical writing… more
- Merck & Co. (Rahway, NJ)
- …Pharmacology and Pharmacometrics --Immune/Oncology-(QP2-IO)-team in the role of-Senior Specialist .--QP2-IO team is part of the Global Clinical Development ... our end-to-end pipeline support in one of the world's most research -intensive biopharmaceutical companies. Senior Specialists in QP2-I/O-will work in collaborative… more
- Merck & Co. (Durham, NC)
- …with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract ... be responsible for activities that support Good Manufacturing Practice and regulatory compliance during product manufacturing within the respective VMF's to include… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Specialist , Manufacturing Automation (Hybrid) g, quality and engineering groups.- -Supports a large spectrum of sophisticated ... within Manufacturing Operations; providing multiple opportunities to learn new automatioThe Specialist is a member of the Focus Factory Automation team responsible… more
- Merck & Co. (Durham, NC)
- …medicines and vaccines, including our HPV vaccines. - The Senior Engineering Specialist will troubleshoot and maintain process and process support equipment utilized ... plant maintenance and spare parts procurement systems. Working knowledge of regulatory requirements in accordance with GMP manufacturing operations Ability to work… more
- Eisai, Inc (Nutley, NJ)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. TheNeurology Account Specialist (NAS) will be part of a diverse team of sales professionals who… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to be part of the team responsible for Warehouse activities that will… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …global function on study and project teamsProduces independent writing for publications and regulatory documentsServes as a specialist in PK-PD and Pop PK-PD ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The primary… more
- Amerantbank (Miramar, FL)
- The BSA OFAC Specialist II is primarily responsible for reviewing and researching potential matches to government sanctions, internal watch lists, and 314a sharing ... areas of the Bank to ensure compliance and correct disposition. The OFAC Specialist conducts special testing reviews to ensure appropriate mitigating controls are in… more
- Cambia Health Solutions, Inc (Portland, OR)
- … research , interpret and understand laws, regulations and other regulatory and compliance guidance.Demonstrated ability to review legal documents regarding ... Privacy Specialist I or II Work from home within...fit. What You Bring to Cambia: Qualifications: The Privacy Specialist I would have a bachelor's degree in law,… more
- MultiPlan (Atlanta, GA)
- …edits, claim factors, guidelines and other applicable reference materials. Monitor, research , and summarize trends, coding practices, and regulatory changes. ... bright people come to shine! The Senior Medical Coding Specialist provides analysis of the highest dollar and most...the highest dollar and most complex claims by applying research , coding standards, industry knowledge and federal regulations to… more
- MultiPlan (Atlanta, GA)
- … Research , Client, Physician Teams as well as Senior Leadership. Monitor, research , and summarize trends, coding practices, and regulatory changes. Assist ... people come to shine! JOB SUMMARY: The Medical Coding Specialist is responsible for providing billing analysis of claims...talking points or tools, and communicating overall industry or regulatory changes which affect the department. Research … more
- MultiPlan (Atlanta, GA)
- …additional negotiation talking points or tools, and communicating overall industry or regulatory changes which affect the department. Monitor, research , and ... summarize trends, coding practices, and regulatory changes. Research and review individual claims, claim trends or detailed itemized bills, operative notes and… more
