- Parexel (Indianapolis, IN)
- …success, we are expanding our esteemed Medical Sciences Team and seeking an Associate / Medical Director to support the growth of our Global Immunology and ... Inflammation Therapeutic Franchise. As an Associate / Medical Director , you...the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated… more
- GRAIL (Indianapolis, IN)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... + MS or PhD with 10+ years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device,… more
- Parexel (Indianapolis, IN)
- …activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility...other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study… more
- Parexel (Indianapolis, IN)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... action (CAPA) development and checks, when applicable **Collaboration** + Reports to Director of Clinical Site Operations (DCSO) or Director … more
- Parexel (Indianapolis, IN)
- …activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... The Senior Clinical Research Associate (SrCRA) has local...other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study… more
- Sumitomo Pharma (Indianapolis, IN)
- …** Medical Director , Clinical Development - Oncology** . The associate medical director is responsible for the leadership, development, and ... management of clinical studies while building and maintaining relationships with investigators...of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory… more
- Elevance Health (Indianapolis, IN)
- ** Clinical Operations Associate Medical Director ** **Carelon Medical Benefits Management** **Radiology Benefit Management/Utilization Review** ... including radiology, cardiology and oncology. _ The ** Clinical Operations Associate Medical Director ** is responsible for supporting the medical … more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. The purpose of the Associate Director / Director Clinical Delivery Capabilities role within Exploratory ... of ICH and quality guidelines needed for successful delivery of the portfolio and clinical trials, the Associate Director / Director possesses the business… more
- CenterWell (Indianapolis, IN)
- …a part of our caring community and help us put health first** The Associate Director , Product Management Conceives of, develops, delivers, and manages products ... for customer use. The Associate Director , Product Management requires a solid...dynamic team of product management professionals dedicated to advancing clinical operations and technology solutions. Drive the strategic roadmap… more
- Bristol Myers Squibb (Indianapolis, IN)
- …aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part ... patients in need. In this role, you will report directly to the Exec. Director , IT and be primarily responsible for implementing RayzeBio's vision for growth and… more
- Elevance Health (Indianapolis, IN)
- ** Medical Director Associate -...**How you will make an impact:** + May provide clinical guidance for pharmacy prior authorizations using CarelonRx ... services to drive affordability and improve member outcomes. The ** Medical Director Associate - CarelonRx** supports...of the US. + Minimum of 5 years of clinical experience; or any combination of education and experience,… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- The Associate Director , Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant ... consistency, and compliance. This position reports directly to the Senior Director , CNS Medical Communications Lead. **Key Responsibilities Include:** **Global… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- … needs and nutraceutical products for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a champion of Otsuka's culture ... responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a… more
- Sumitomo Pharma (Indianapolis, IN)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical … more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Associate Director is responsible for developing publication strategies and plans. The ... Associate Director will draw upon information from...Medical Affairs, Value Evidence & Outcomes (VEO), Global Clinical Development, Preclinical Development as well as commercial colleagues… more
- Lilly (Indianapolis, IN)
- … clinical trial medicines, while also reducing costs and environmental impact. The Associate Director of Materials will lead the planning and procurement of ... direct materials supporting clinical supply manufacturing across small molecule, biologics, and peptides at the Lilly Medicine Foundry. This role ensures on-time… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of ... clinical and commercial controlled substances manufactured at CMOs under...a minimum of 5 business days. **Company benefits:** Comprehensive medical , dental, vision, prescription drug coverage, company provided basic… more
- Lilly (Indianapolis, IN)
- …will help solve our world's greatest health challenges. **Purpose:** The purpose of the Associate Director Informaticist role is to support the design of ... clinical programs and trials by bringing together internal and...in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical , dental, vision and prescription drug benefits; flexible benefits… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products ... biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- The Associate Director , Strategic Planning & Operations will support the assets of varying lifecycle stages in the relevant therapeutic area portfolio. This role ... in driving operational excellence and innovation within our Global Medical Affairs organization, with a specific focus on the...are in place. This position reports directly into the Director , Strategic Planning Lead, who in turn reports into… more
