Lead clinical pharmacology activities related to study design, protocol development, study execution, reporting and interpretation of data. Conduct PK and PK/PD analysis . Work closely with pharmacometrics team members and provides input related to analysis and reporting of PK and PK/PD. Lead development of clinical pharmacology sections for regulatory filings including a

Legal Collections Associate Remote Job Locations US NJ MORRISTOWN | US AR CONWAY | US IL CHICAGO | US MI SOUTHFIELD | US NY NEW YORK | US NJ JERSEY CITY | US GA Alpharetta | US NJ CHERRY HILL Job ID 2024 3776 Category Finance Type Regular Division Surplus & Specialty Crum & Forster Company Overview Crum & Forster (C&F) with a proud history dating to 1822, provides special

US Regulatory TA Strategy Develop and execute US regulatory strategy, with oversight as needed, and in conjunction with Global Regulatory Lead (GRL), Global Regulatory Team and Global project teams. Partner with the GRL to understand the competitive landscape, e.g., views of US HAs, regulatory precedents, labeling differences and TA specific issues. Utilize US regulatory

What you'll need We look for candidates who strive to push the state of the art in areas like generative deep learning for image and video processing and recommendation systems. Ph.D. or MS in CS, Engineering or other quantitative fields and 4+ years of research and development experience in building scalable ML systems. Expertise with contemporary techniques/tools for Co

PDI is seeking a Clinical Scientist II Microbiology to conduct antimicrobial testing, method development, and develop the strategy, design, execution, and interpretation of clinical trials in support of early drug development. Primarily, the role supports new market launches with input across all facets of project progression including scientific insights, prototype asses

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

The CTMS Business Analyst is responsible for providing high quality calendar builds and accurate financial entry services (service deliverables) for site clients who utilize a Clinical Trial Management System for clinical research financial oversight and patient enrollment management. WCG SSU services are culminated by the CTMS service deliverables, triggering the start d

Primary Work Address Dept of Molecular Biology, Princeton, NJ, 08544 Current HHMI Employees, click here to apply via your Workday account. The Bassler lab at Princeton University has an opening for a Research Technician to aid in research projects exploring how bacteria communicate and orchestrate group behaviors using a process called quorum sensing. Quorum sensing contro

JOb Title Associate Scientist. Job Id 24 02124 Location East Hanover,NJ Duration 12 Months on W2 Contract Bachelor of Science Degree in relavent field. 2 years of analytical analysis experience preferred. Working as part of a project team, you support the delivery of long term research projects in line with the business and consumer needs. You plan and execute projects fr

The Associate Director, Regulatory Affairs CMC will be responsible for leading global regulatory CMC strategy for product development and registration, and for preparation of CMC dossier for primarily small molecule regulatory submissions (INDs and NDAs) according to global regulatory expectations and requirements. This position works cross functionally with Regulatory Af

Senior Scientist (Hybrid) About Us Join Hartz, where our love for pets drives everything we do. With over 95 years of commitment to pet care excellence, we are a trusted household name across the United States. Innovation is at the heart of our mission as we continuously strive to provide products that nurture the special bond between pets and their owners, ensuring they

Lead and manage multiple commissioning / qualification / validation activities performed at facility with minimal supervision. Equipment Qualification / Re Qualification (IQ, OQ, PQ) for process equipment, QC equipment, packaging equipment, clean utilities. Cleaning Verification / Validation studies for transferred products. Media Fills / process simulations protocols. En

Ensure that the requirements of the client are well defined, understood, and communicated to the laboratory staff. making sure samples are logged and process in LIMS properly. Ensure that each client project is adequately serviced by the laboratory. Schedule bottle delivery and pickup and workout all logistic part with client. Make sure your projects are complete in timel

The Clinical Trial Documentation Specialist position is based within our Clinical Operations group, and works with departmental management and the Principal Investigator in the implementation of project clinical trial protocols. Job Type Full Time Base Hours 9 00AM 6 00PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be a

Client Summary Our client is a leading not for profit health care organization that is the largest, most comprehensive and truly integrated health care network in New Jersey, offering a complete range of medical services, innovative research and life enhancing care. Job Description Staff Pharmacist The Staff Pharmacist, Pharmacy Per Diem, Certified Pharmacist, and Staff P