include Performing animal surgery, behavior assessment, and care relating to gene therapy for spinal cord injury; tissue sectioning and immunohistochemistry for analysis of tissue; managing the production and quality control of AAV and lentiviral production for the Smith lab and a few other labs at Temple, requiring good manufacturing practice to produce high quality recom

Prepares /oversees the preparation of various regulatory submissions including Pre Submissions, 510(k) submissions, CLIA Waiver Applications, Dual 510(k)/Waiver by Applications, technical files, and license applications. Monitors new and changing regulations and guidance and disseminates information to stakeholders. Identifies regulatory trends and conducts key regulatory

PHARMACY TECHNICIAN Job Locations US PA WILKES BARRE ID 2024 143716 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Join our PharMerica team! PharMerica is a closed door pharmacy where you can focus on fulfilling the pharmaceutical needs of our long term care and senior living clients. We offer a non retail pharmacy environment. Our org

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply t

Technician II RDVI #N/A TEAM provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic p

include but are not limited to Manage & track progress for ongoing Medical Affairs projects, including developing project charters and plans Plan, implement, and maintain new and existing departmental platforms Oversee vendor management and serve as a liaison between vendors and Medical Affairs staff Collaborate with internal stakeholders including Regulatory Affairs, Clin

Company Description Join us and make YOUR mark on the World! Are you interested in joining some of the brightest talent in the world to strengthen the United States' security? Come join Lawrence Livermore National Laboratory (LLNL) where our employees apply their expertise to create solutions for BIG ideas that make our world a better place. We are committed to a diverse a

The Senior Manager, Quality Control Analytical will report to the Director of the Quality Control Analytical team at the Resilience Philadelphia site. This motivated and organized individual with strong people skills will provide supervision and technical expertise to the QC Analytical laboratory while maintaining open communication channels to meet the needs of the organ

The Assistant Director of Content Strategy for the Fox School of Business is responsible for developing content designed to enhance the overall reputation of the school, to communicate the Fox/STHM story to various stakeholders. The Assistant Director will primarily focus on publication efforts for the Fox Focus (Alumni magazine), On the Verge (Research magazine), and Con

The Technology & Data Solutions (TDS) business unit is the Syneos Health accelerator for life sciences innovation. TDS houses our advanced technology acquisitions, homegrown products & applications, actively participates in new M&A and partnership activities, delivers critical insights as part of our integrated strategy for customers and drives enterprise wide adoption an

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

/JOB PURPOSE Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations. Coordinates, compiles, and tracks product applications to regulatory agencies. Essential Duties And Responsibilities Review clinical site regulatory documents t

Singular talents thrive as an Associate Director of Medical Writing with Caudex. We advocate. We captivate. We cogently demonstrate. We combine gravitas with that lightness of touch that only comes from genuine, deeply held mastery and passion. We're recognised leaders in our field because we make the extraordinary seem effortless. We are your people. You're a recognised,

What this job involves Join JLL for a great opportunity to support a world class life sciences client. The Sr. Manager, Planning & Scheduling is a new investment role and will be responsible for the management of a large team of site based planners and schedules across a network of facilities located throughout United States and Puerto Rico. All work performed is in accord

SHIFT Weekends (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions ma