- Lilly (Indianapolis, IN)
- …position 3 days onsite/2 days remote **Purpose:** This role is responsible for trial level clinical data strategy including database structure, content ... with key study partners to define, implement, and deliver clinical data management packages. This role is... trial leadership and ownership for a particular trial , set of trials , or programs. **Primary… more
- Lilly (Indianapolis, IN)
- …channel strategy, and preparation of final reports and publications. + Participate in reporting of clinical trial data in Clinical Trial Registry ... of responsibility, the development, conduct and reporting of local clinical trials ; the implementation of global ...I and II studies where applicable), as well as non- clinical trial solutions/activities that are conducted in… more
- Lilly (Indianapolis, IN)
- …of external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... gastroenterology therapeutic area will support early and late phase clinical trials for assets in the gastroenterology...clinical data relevant to the molecule. Clinical Research/ Trial / Execution and Support + Plans,… more
- Lilly (Indianapolis, IN)
- … Study Build Programmer is responsible for leading and programming and testing clinical trial data collection databases, including the mapping, testing ... and associated data repository mappings for a trial or set of trials within a...a deep understanding of the technology used to collect clinical trial data + Effectively… more
- Sumitomo Pharma (Indianapolis, IN)
- …International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to ... 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
- Lilly (Indianapolis, IN)
- … dissemination, and preparation of final reports and publications. + Participate in reporting of clinical trial data in Clinical Trial Registry ... activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing...area of responsibility, the development, conduct and reporting of clinical trials ; the implementation of global … more
- Parexel (Indianapolis, IN)
- …+ 7+ years experience in pharmaceutical/biotech clinical data management / Biometrics ( clinical trial data and/or Real World Data ) + Medical ... affairs experience (Phase IIIB - IV trials experience); Late Phase Oncology + Strong project management...techniques. + Experience in leading DM study teams, overseeing trial data activities, and collecting clinical… more
- Lilly (Indianapolis, IN)
- …Clinical Design Capabilities in the development of clinical plans and clinical trial designs (eg reference trials , design analytics, country ... focus and expertise. More about the role: **_Clinical Plan, Trial Options and Clinical Trial ...to deliver on new regulatory expectations (eg decentralization of clinical trials , increase racial and ethnic diversity… more
- Parexel (Indianapolis, IN)
- …is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study ... and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg enrollment, database release), to safeguard the… more
- Lilly (Indianapolis, IN)
- …+ Leverage robust knowledge of multiple inventory methodologies to collaborate with Clinical Trial Study Management and facilitate optimal Supply Planning. + ... + Maintain GMP/GCP compliance by following procedures applicable to clinical trial execution. + Actively participate in...+ Provide ongoing support and maintenance for all Lilly clinical trials utilizing IWRS. + Provide consultation… more
- Lilly (Indianapolis, IN)
- … data safety monitoring boards, medical monitoring) + Reviews and evaluates emerging clinical trial data and oversees data interpretation; supports ... registry trials / studies) + Supports the clinical operations team, including clinical trial...(eg, slide decks, posters, manuscripts, abstracts, etc.) based on clinical trial data + Supports… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …Provide medical and scientific leadership to cross-functional study teams and ensure high-quality clinical trial design, conduct, and data interpretation. + ... human health. OPDC develops promising drug candidates, starting with clinical trial management, and then planning the...to post commercialization, with emphasis on the large global clinical trials and regulatory filing activities. The… more
- Parexel (Indianapolis, IN)
- …is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study ... and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg enrollment, database release), to safeguard the… more
- Norstella (Indianapolis, IN)
- …Sponsor/CRO/Partner environment + Experience using data analytics and services to solve clinical trial challenges + Understanding of how, and where, AI can ... + Protocol Design, Country, Site and Investigator Feasibility + Clinical trials operations, cost benchmarking & landscapes...+ Deep knowledge and expertise of the pharma strategic Clinical trial landscape (Clin Dev/Ops, clinical… more
- Lilly (Indianapolis, IN)
- …for site selection, investigator meetings, steering committees, and clinical trial training. + Participate in data analysis, scientific dissemination, and ... is pivotal in the design, execution, and analysis of clinical trials that support the development of...for compliance of team members. + Lead completion of clinical trial documents including protocols, amendments, investigator… more
- Sumitomo Pharma (Indianapolis, IN)
- …TLFs, and the clinical data output + Contributes to interpretation of clinical trial results and the writing of clinical study reports + Contributes ... and participate in study set up and design including data collection tools, data analysis, eCRF design,... trials in both early- and late-stage clinical development, especially protocol development and trial … more
- Datavant (Indianapolis, IN)
- …impact. + Deep understanding of CRO operations, data workflows, and the intersection of clinical trial data with RWD. + Knowledge of data privacy, ... teams to operationalize our CRO partnerships, ensuring Datavant's capabilities in ** trial tokenization** , **real-world data (RWD) connectivity** , and… more
- Lilly (Indianapolis, IN)
- …image analysis group to support quantitative analysis of images obtained within clinical trials across therapeutic areas such as Oncology, Diabetes, Immunology, ... and Neurodegeneration. In Oncology clinical trials , the individual will serve a...PET, SPECT, CT, and MRI + Author and review clinical trial documents (protocols, study reports, and… more
- Lilly (Indianapolis, IN)
- …Collaborate with clinical research staff in design, conduct and reporting of clinical trials + Review and approve risk profiles to ensure appropriate ... Safety. _Data Dissemination and Scientific Exchange_ + Participate in data analysis and preparation of final reports and publications....industry including the design and implementation of large global clinical trials . + Minimum of five years… more
- Deloitte (Indianapolis, IN)
- … data architecture, and data mapping + Experience with solutions for data -driven trials and clinical development insights (ie: site burden, patient ... to build, deploy, and operate integrated/verticalized sector solutions in software, data , AI, network, and hybrid cloud infrastructure. These solutions are powered… more