Project Administration Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ensure quality, completeness and inspection readiness Coordinates and monitors the activities associated with study deliverables across all applicable internal functional departments and vendors. Assists with activities associated with interim analyses, d

providing superior service and care. Position Specific Benefits include You are eligible for up to 180 hours of paid time off per year based on your Full or Part Time status. We also offer a number of employee discounts to various activities, services, and vendors... And employee parking is always free! Position Staff Pharmacist 38.4/ hours/week Shift Night Shift 7 on 7 o

PHARMACY TECHNICIAN Job Locations US PA HORSHAM ID 2024 143149 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Provides a variety of pharmacy technician, data entry , billing and IV technician functions to support clinical and business operations for the assigned region . Responsible for coordinating , and may also train these activitie

The Sr Pharmacy Fraud Investigations Analyst is responsible to conduct timely and thorough health care fraud investigations on behalf of the Company. Investigations are confidential and are conducted in accordance with SIU Policies and Procedures, contractual obligation and in accordance with applicable state and federal regulation. Conducts investigations in accordance w

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

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

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

Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transforms patients' lives. Through our unique approach to gene science based on Nobel Prize winning technology, we are moving forward rapidly to bring innovative therapies to market. At Lexicon, our passion and dedication are driven by the patients for whom we work. Lexicon employees are i

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,

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

(Objective) The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. Main activities Prepare sample for analysis by recording, weighing, and blending Write identification onto plates so that client and sample number can be tracked Pipette sample solution into tubes or plates according to the analysis process bei

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,

Collaborates with physicians and other providers to screen potential patients for eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials. Coordinates patient care in compliance with protocol requirements. Dispenses investigational drug and provides patient teaching regarding 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