- 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. (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. (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. (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. (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)
- …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. (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
- 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
- Fenway Health (Boston, MA)
- …the guidance of the Director of Nursing, Nursing Professional Development Specialist is responsible for leading professional development initiatives to promote ... and evidence-based practice within Fenway Health. The Nursing Professional Development Specialist will implement Evidence Based Practice changes through policy and… more
- ChristianaCare (Newark, DE)
- Are you seeking an amazing nurse leadership role as a Clinical Nurse Specialist with our Perioperative Services team? Christiana Hospital & Wilmington Hospital is ... retirement, a 403(b) and a defined contribution plan.We are seeking a Clinical Nurse Specialist to work the Day Shift. The selected individual will function as a… more
- Lifespan (Providence, RI)
- …the people within our communities. We are seeking a Sr. Compliance and Privacy Specialist to join our Internal Auditing department in Providence, RI. This is a ... as the Privacy Resource Person to employees in their absence Cooperate with regulatory , third party and external auditors and consultants, review results of test… 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
