- Edwards Lifesciences (Indianapolis, IN)
- …/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols, GCP ... Monitor ** to join Edwards Aortic Field Monitoring team. As a Senior Clinical Research Monitor , you ensure trial patients' safety by assuring trials are… more
- Sumitomo Pharma (Indianapolis, IN)
- …execute corporate clinical strategy for global development projects in Oncology + Monitor clinical trial progress, identify and mitigate risks, and make ... from preclinical experiments to the end of the product's life cycle. + Clinical Trial Oversight: Develop and oversee clinical trial strategies, ensuring… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. **Associate - Clinical Trial Foundations** **Purpose:** Clinical Trial Foundations as ... Analytics (CDDA) provides leadership in the strategy and development of contemporary clinical trial processes, technologies, information, and capabilities and in… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. Purpose: The Associate Director, Clinical Trial Foundations (CTF), will serve as the subject matter expert for ... clinical systems supporting clinical development. In this...improvements + Develop critical success factors for pilots/projects and monitor progress to ensure clear criteria exists to enable… more
- Lilly (Indianapolis, IN)
- …product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing to ... of phase 3b/4 studies **,** as well as non clinical trial solutions/activities that are conducted in...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
- Lilly (Indianapolis, IN)
- …external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... and clinical data relevant to the molecule. Clinical Research/ Trial Execution and Support + Plans,...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
- Bausch + Lomb (Indianapolis, IN)
- …Summary** **:** Is responsible for the implementation and oversight of clinical study operations by organizing and coordinating with other relevant parties ... the planning, implementation, management, execution and completion of clinical studies according to applicable regulations and guidance, ICH and GCP, and Bausch &… more
- Cytel (Indianapolis, IN)
- …2 years in clinical data management. + Strong understanding of clinical trial processes and data management workflows. + Excellent organizational, ... and integrity come together to advance the state of clinical development. **Who Are You?** We are seeking a...of project activities across multiple workstreams. + Maintain and monitor detailed project timelines, ensuring deliverables are met on… more
- Lilly (Indianapolis, IN)
- …are determined to make life better for people around the world. **Purpose:** Clinical Trial Foundations (CTF) delivers innovative and reliable supplies, systems, ... processes, and information to enable clinical development and speed medicines to patients. The Associate Director/Director, CTF Clinical Development Operating… more
- Lilly (Indianapolis, IN)
- …sites across all geographies. + Interpret global field intelligence to influence clinical trial design elements (eg inclusion/exclusion criteria, visit burden), ... with clinical development teams, ensuring alignment between TA priorities, trial design, patient engagement priorities making data informed decisions + Partner… more