Clinical Research Associate Jobs in Indiana, United States

Clinical Research Associate at IQVIA Biotech partners with biotech companies to accelerate clinical development. Responsible for onsite monitoring of clinical trial sites, ensuring compliance with GCP, ICH, and sponsor protocols.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Study Delivery team at AstraZeneca ensures clinical studies are executed efficiently and in compliance with regulations. The Clinical Research Associate manages site initiation, monitoring, and closure across Ohio and Michigan, performing both onsite and remote visits, data verification, and regulatory documentation.

Clinical Research Associate at AstraZeneca, responsible for delivering clinical studies at assigned sites, managing study start‑up, monitoring, and closure while ensuring compliance with ICH‑GCP and local regulations. The role conducts onsite and remote monitoring visits, updates CTMS, and collaborates with local study teams and investigators.

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

Clinical Research team at Merck conducts oncology trials across the United States. The Clinical Research Associate ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional partners.

Clinical Research team at Merck conducts immunology trials, ensuring protocol compliance and patient safety. The CRA manages site relationships, performs remote and onsite monitoring, and oversees regulatory documentation across multiple US locations.

Clinical Research Operations at Merck conducts cardiovascular, vaccine, and infectious disease trials. The Clinical Research Associate monitors site performance, ensures compliance with ICH/GCP, manages documentation, and supports site selection and expansion.

Clinical Research Associate II on the Immunology team at AbbVie, advancing the pipeline by ensuring high‑quality clinical trial execution. The role partners with investigators and site staff to drive data integrity, compliance, and patient recruitment while providing training and risk‑based monitoring.

Clinical Research team at Thermo Fisher Scientific conducts multi‑site oncology, ophthalmology and neurology trials. The CRA II monitors investigator sites remotely, performs risk‑based assessments, ensures ICH‑GCP compliance, and documents findings.

Clinical Research Associate II - Neuro & Immunology role at AbbVie focuses on advancing the company's pipeline by ensuring high‑quality clinical trial execution and site engagement. The CRA II partners with investigators and site staff to monitor trials, train sites, and drive data integrity and compliance across neuro and immunology studies.

Clinical Research Associate II on AbbVie’s Neuro & Immunology team, advancing the pipeline by ensuring rigorous site clinical research and data integrity. The role serves as the primary site contact, training and motivating investigators, conducting monitoring and risk assessments, and leveraging CRM tools for engagement.

Caption Health’s Clinical Research Associate supports medical device trials, ensuring GCP and ISO 14155 compliance. The role monitors sites, verifies data, writes reports, and manages training and deviations.

Clinical Research Associate (CRA) in Cell Therapy at AstraZeneca oversees study delivery at sites in Chicago or Wisconsin. Works with local study teams, monitors compliance with ICH‑GCP, GMP/GDP, and local regulations.

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

Premier Research’s Global Clinical Monitoring and Site Management team builds the bridge between biotech, medtech, and specialty pharma companies and the patients who need new medicines. As a Clinical Research Associate I, you deliver quality monitoring reports, conduct site visits—remote or on‑site—ensuring data integrity and patient safety, and collaborate with the Clinical Lead to proactively resolve trial issues.

FSP Clinical Research Team conducts oncology trials to advance cancer therapies. The CRA monitors study sites, conducts pre‑study and initiation visits, ensures protocol compliance, reviews CRFs, reports serious adverse events, and supports site staff.

Clinical Research team at Merck conducts ophthalmology trials across the United States. The Senior Clinical Research Associate manages site relationships, ensures protocol compliance, and leads monitoring activities both remotely and on‑site, mentoring junior CRAs.