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.

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.

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate (CRA) – Animal Health, you will be a key member of the global Research & Development organization, supporting the execution of clinical studies for our innovative Farm Animal and Pet Health products. You will be responsible for ensuring studies are conducted to the highest standards, that data is captured accurately, and that we maintain compliance with all global regulatory guidelines.

Job Overview Provide strategic quality leadership and oversight across assigned Quality Assurance (QA) programs, with a strong focus on clinical research, clinical operations, pharmaceutical development, and GxP-regulated activities. Influence quality outcomes across multiple functional areas, business units, and customer engagements through expert guidance, risk-based decision making, and oversight of quality systems and compliance programs.

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5+ years of monitoring residing in the Midwest area.

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US.

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' r

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.

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.

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.

Clinical Services team at Iterative Health coordinates industry-sponsored clinical trials to accelerate therapeutic development. The Clinical Research Coordinator II independently manages study start‑up through closeout, oversees patient recruitment, conducts protocol visits, and ensures regulatory compliance.

ObjectiveHealth Clinical Research team ensures high‑quality clinical trial data entry and compliance. The specialist accurately enters and reviews participant data in EDC systems, resolves queries, and maintains audit trails to support study milestones.

The Clinical Research Coordinator II independently coordinates and manages clinical research studies involving human participants in accordance with study protocols, Good Clinical Practice (GCP) guidelines, regulatory requirements, and organizational policies. This role is responsible for participant recruitment and enrollment, informed consent, study visit coordination, data and documentation management, regulatory compliance, subject safety monitoring, and collaboration with investigators, spo

Clinical Nurse-Research IU Health Arnett Hospital | Full-Time | Monday-Friday | Days IU Health, Indiana's #1 healthcare system, is seeking a dedicated Clinical Research Nurse to join our team at IU Health Arnett Hospital. This role offers a unique opportunity to combine direct patient care with clinical research that helps advance new treatments and improve patient outcomes.

At Innovative Hematology, Inc. (IHI), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

Our leaders shape strategic initiatives, develop passionate teams, and work to improve health outcomes. They advance our mission and exemplify excellence, compassion, teamwork and purpose in all that they do .

The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values.