Clinical Research Associate Jobs in Indiana, United States

Clinical Research team at Cook Medical leads the oversight of vendor CRAs and monitoring activities for medical device studies. The role mentors and trains vendor staff, ensures compliance with FDA, ISO-14155 and study protocols, and drives process improvements in monitoring strategy.

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

Clinical Operations team at Worldwide Clinical Trials drives innovative clinical studies across therapeutic areas. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, ensures regulatory compliance, and supports data collection for CNS trials.

Merck seeks a Senior Clinical Research Associate to manage ophthalmology clinical trials across the US. The role ensures site compliance with ICH/GCP standards, monitors study conduct, and mentors junior staff while maintaining strong investigator relationships. This is a fully remote position requiring residence in specific states.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the Central Region to deliver high-standard clinical trial monitoring and participant care across a remote territory spanning multiple states. Day-to-day, the role covers full-cycle site monitoring, pre-study and initiation visits, CRF review and query resolution, SAE reporting, and registry management, with 8-10 on-site days per month.

At Elanco's global Research & Development organization, the Clinical Research Associate (CRA) – Animal Health supports the execution of clinical studies for Farm Animal and Pet Health products. Day-to-day, you perform and manage clinical monitoring activities, serve as the primary contact for trial sites, conduct data review and source data verification, mitigate site-level risks, and collaborate with cross-functional partners to ensure study compliance and data integrity.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

Connected Devices at IQVIA Clinical Research drives device strategy and data ingestion to meet trial endpoints. The Associate Director leads client relationship management, oversees quality control, capacity planning, and collaborates with Business Development on proposals.

Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Associates (CRA 1) for Oncology, CAR T, or Ophthalmology trials. The role involves site monitoring, data integrity verification, SAE reporting, and supporting study site operations across Central or West coast US hubs or Montreal, Canada.

Research team at Innovative Hematology, Inc. conducts clinical studies to advance treatments for rare blood disorders. The Clinical Research Coordinator executes study protocols, manages budgets, coordinates patient care, and ensures regulatory compliance.

Versiti Research team supports clinical studies by collecting biospecimens, processing samples, and managing study data. The Assistant, Clinical Research handles phlebotomy, specimen processing, data entry, and administrative tasks to ensure research timelines are met.

Profound Research partners with community physicians to offer clinical trials as a therapeutic option, handling infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. As a Clinical Research Coordinator I, you will serve as the primary coordinator for assigned studies at one of our sites, managing study activities from start-up through closeout, leading patient visits, and maintaining audit-ready documentation.

Clinical Research team at Hematology Oncology of Indiana conducts oncology trials to advance patient care. The RN Clinical Research Coordinator independently manages complex phase 1‑3 studies, ensuring protocol compliance, regulatory adherence, and accurate data capture.

Franciscan Health Indianapolis Campus conducts clinical research to advance patient care. The Clinical Research Coordinator obtains informed consent, trains team members, manages protocol procedures, and ensures accurate billing and documentation.

ObjectiveHealth’s Clinical Research Coordinator I team drives patient enrollment and protocol execution for trials in Gastroenterology, Urology, Dermatology, and Oncology. The role manages IRB‑approved study workflows—screening, randomization, consenting, blood draws, ECG, and medication administration—while ensuring data integrity and regulatory compliance.