- Parexel (Indianapolis, IN)
- **Job Summary:** Core member of the Clinical Trial Team (CTT), independently managing all vendor-related aspects of global clinical trial (s) to deliver ... + Very strong vendor management skills; outsourcing, contracting, and sourcing of clinical trial services + Results-driven: demonstrated ability of completing… more
- Parexel (Indianapolis, IN)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Parexel (Indianapolis, IN)
- …information to create investigator/institution entities within the CTMS system to then enable site association with a clinical trial ; routinely reconciles ... Parexel FSP has an exciting opportunity in Site Start Up! The Associate Manager,...Trial Master File; Captures relevant study, country and site level information and milestones within the CTMS system… more
- Parexel (Indianapolis, IN)
- …in Lupus is preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
- Sumitomo Pharma (Indianapolis, IN)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Sumitomo Pharma (Indianapolis, IN)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The medical… more
- Bristol Myers Squibb (Indianapolis, IN)
- …role, the Warehouse Associate shall provide tactile support of all clinical trial and future commercial receiving, material handling, shipping and ... for warehousing support related to domestic and international shipping and distribution of clinical trial and commercial products for RayzeBio programs. In this… more
- IQVIA (Indianapolis, IN)
- …candidates located East, Central or West Coast. **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... IQVIA Early Clinical Development is hiring for CRA 2. Ideal...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site… more
- Lilly (Indianapolis, IN)
- …resilience as the site evolves from a design concept to a GMP clinical trial site . **Key Responsibilities:** + Responsible for establishing a technically ... develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental… more
- ThermoFisher Scientific (Indianapolis, IN)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... needs. In this client dedicated role, you will work on- site to provide administrative and technical support by performing...performing day-to-day functions within the client organization to support clinical trial activities. **A Day in the… more
