- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... is expansive, stretching across all functional areas of the site , requiring the Associate Director Operational Readiness to build breadth of knowledge and… more
- System One (Plainsboro, NJ)
- …Documentation Governance - Manage the filing, oversight, and retrieval of safety trial documentation within the Veeva Vault Clinical (eTMF), Quality and ... Title: Global Drug Safety and PV Compliance Associate Location: Must be local for hybrid schedule...(un)announced inspections and (partner) audits conducted at the US site . - Ensure real-time support and documentation retrieval during… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director, Supply Chain will provide technical and business...processes + Work with process owners, Global Supply Chain, Site Supply Chain Teams, and Business Quality Assurance to… more
- Cedars-Sinai (Los Angeles, CA)
- …the role of host defense in lung inflammation and fibrosis. The Research Associate II will perform routine and increasingly complex laboratory tasks and procedures ... maintenance. This position does not have supervisory responsibilities. The associate investigates molecular mechanisms of lung fibrosis, and participates in… more
- ThermoFisher Scientific (Devens, MA)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development...is a fully onsite role based at our customer's site in Devens, MA. We welcome applicants from all… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Sr. Principal Associate for Analytical Quality Assurance ensures that laboratory activities...partners are carried out in accordance with global and site quality standards and/or are following current Good Manufacturing… more
- University of Pennsylvania (Philadelphia, PA)
- …(3) years). Applicants must have a Ph.D. degree. Responsibilities may include management of on- site activities for a new trial based out of the Connecticut Army ... of Medicine at the University of Pennsylvania seeks candidates for a Research Associate position in the Academic Support Staff. This appointment will be initially… more
- Lilly (Indianapolis, IN)
- …semi-finished drug product batches for Indianapolis Parenteral products, including commercial and clinical trial materials to ensure high quality medicine (GMP ... productivity within the Batch Disposition work center and/or the site . + Ensure regular presence in operational areas to...programs and quality systems. + Lead, Mentor, and Coach Site personnel on quality matters associated with the Batch… more
- System One (Tucson, AZ)
- …or internal audits and inspections when called upon as either a sponsor or a trial site . + Communicates results of experiments and may present findings at ... our client's clinical laboratory team as a Clinical Laboratory Associate . This role is ideal...setting. Knowledge, Skills, and Abilities: + Experience documenting detailed Clinical Trial activities in Case Report Forms,… more
- University of Maryland, Baltimore (Baltimore, MD)
- …who are already exploring how data science can be merged with clinical trial methodologies in the context of a multi- site health system to facilitate ... scientist or physician-scientist with expertise in real world data and novel clinical trial design/execution with particular emphasis on oncology sciences to… more