PHARMACY TECHNICIAN Job Locations US PA BETHLEHEM ID 2024 143339 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 organi

The Principal Scientist stability is accountable for the stability program on assigned brand (s) and acts as Stability Product Lead. Participates on transfer team for new products to internal and external sites (as required), reviews registrational stability studies and conducts gap analysis against Global Manufacturing & Supply requirements. Develops stability data where

Do you want to work at one of the top 100 hospitals in the nation? Our amazing Pharmacy Team dispenses approximately 6,200,000 individualized patient doses per year, as well as 170,000 retail/mail order prescriptions. We provide medications that are safe and efficacious. Life is full of choices, and whom you work for is one of life's most meaningful decisions. ChristianaC

Responsible for creating a patient profile in the pharmacy information system. Enters necessary prescription plan information in the patient profile for processing and adjudicating patient's prescriptions. Responsible for entering all new patient prescription information into the pharmacy information system. Addresses insurance, reimbursement, and payment issues as approp

Supports client projects through early translational to late development for clinical pharmacology and quantitative analyses Collaborates with internal and client teams on regulatory, clinical development, clinical, pharmacology, pharmacometric and another drug development issues Assist Project Leaders in writing and compiling reports and other documents summarizing advic

Staff Pharmacist Part Time Rockford Center Newark, DE As a Part Time nonexempt CPS Solutions, LLC Staff Pharmacist , you will fill orders with accuracy; check technician prepared products before release; maintain the security of pharmacy and controlled substances; enter orders and patient information with accuracy; aid in the training of new staff; update the Director abo

1 Inhouse CRA/ Remote CRA 1 CRC (Major site Oncology part CRC preferred) , . Key Accountabilities Start up (from site identification through pre initiation) Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start up phase. Build relationships with investigators and site staff. Conduct, drive and manage country sp

In this role, you will work with consultants, member hospitals, Vizient regional offices and internal Vizient business units to optimize pharmacy consulting services between Vizient and the member(s) we serve. You will generate new consulting offerings, develop relationships withhospital executives, administrators, clinicians, directors of pharmacy, key opinion leaders an

Establishes credibility throughout the organization and sets an example as a proactive leader who earns respect by demonstrating a sound understanding of business objectives/goals. Exhibits influence and decision making in the areas of leadership and management, change management and operational transformation, organization development and design, performance management,

The Associate Director, Clinical Evidence and Guidelines (The Associate Director) will serve as an ECRI subject matter expert in the areas of clinical evidence, guidelines, and methodology. The Associate Director's responsibilities include identifying short and long term business development opportunities in the realm of clinical evidence, serving as the lead educator reg

This position has the responsibility to support category management and Supply Chain team to create and improve processes, strengthen collaboration, and lead cross functional projects together with other stakeholders (Suppliers, Factories & Product management) to achieve full availability of products at lowest cost and reduce the lead time of New and resourced products to

Develops scientific understanding of assigned program and protocol requirements Supports protocol design and development strategy for clinical trials Manages protocol development process; including writing support, reviewing, adjudication/resolution of cross functional comments, and ensuring high quality final document Contributes to the development of Informed Consent Fo

/JOB PURPOSE The Associate Clinical Supplies Director designs, develops, and implements the clinical supplies strategy to ensure appropriate processes are established and clinical supplies deliverables are met for clinical trials. This individual also manages clinical supply activities including planning and forecasting of clinical supply, oversight of clinical packaging,

Rutgers, The State University of New Jersey, is seeking a Laboratory Assistant for Dr. Tina Liu's lab in the Center for Advanced Biotechnology & Medicine. This position will assist the the PI, Dr. Liu, with routine lab operations, preparation of reagents, and application of experimental methods to support research projects. Among the key duties of this position are the fo

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specif