- Merck & Co. (Philadelphia, PA)
- Job DescriptionThe Associate Specialist of Regulatory Planning & Publishing works closely with various stakeholders of regulatory and safety submissions to ... job role skills and regulatory knowledge. Shared Services: ( Regulatory Submission Specialist )-Provide regulatory submission/systems support.-Manage … 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. (Durham, NC)
- …with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract ... and attendant quality control problems. Basic understanding of GMPs and of regulatory requirements as they apply to the vaccine, sterile pharmaceutical or related… 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)
- …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. (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. (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. (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)
- …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
- 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
- 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
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …global function on study and project teamsProduces independent writing for publications & regulatory documentsServes as a specialist in PK-PD and Pop PK-PD ... hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clinical Pharmacology and Pharmacometrics/… more
- Atrium Health (Charlotte, NC)
- …RAPS, etc.) preferred.Atrium Health Job ID #6301-121284. Posted job title: Oncology Research Specialist /RN - Atrium Health Levine Cancer Clinical Trials ... Type: Staff Overview Job Summary Assists with the coordination of clinical, regulatory , business, and other research - related activities and documentation for… more
- Kellogg Community College (Bedford, MI)
- …processes are in place, including monitoring and effectiveness. * Proactively research , identify and propose ongoing improvements to benefit plans for employees ... and recommend appropriate interventions. * Work with Finance Director and payroll specialist to ensure the continued compliance with ACA, year-end reporting and … more
- Bank of America (Dallas, TX)
- Oil & Gas Regulatory & Research Specialist - SAM Associate II Dallas, Texas **Job Description:** At Bank of America, we are guided by a common purpose to ... **Responsibilities:** We are looking for an energetic, self-motivated, and experienced Regulatory Compliance and Research Specialist to ensure… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist C (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist C Job Description Summary Regulatory Affairs as a field is concerned with ensuring that clinical … more
- UCHealth (Loveland, CO)
- …experience The UCHealth Research Administration Program is seeking a Clinical Research Regulatory Specialist . This position will primarily support ... Preferred candidates will have experience in supporting the conduct of clinical research , regulatory processing and submissions involving central IRBs and IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical Research Regulatory Specialist B Job Description Summary The Abramson ... CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to...regulatory experience preferred. Experience conducting high risk biomedical research and/or oncology regulatory research … more
