Clinical Research Associate - 170044

Responsibilities: of the Clinical Research Associate (CRA): Conduct onsite and remote monitoring activities to evaluate study progress, participant safety, and protocol compliance. Lead site activation efforts, including investigator training and study start-up readiness assessments. Review clinical data, source documentation, and regulatory records to ensure accuracy and completeness. Partner with investigative sites and internal study teams to address findings, resolve issues, and maintain study timelines. Support ongoing oversight of clinical trials through routine travel, monitoring visits, and site relationship management. Qualifications: of the Clinical Research Associate (CRA): Bachelor's degree in Life Sciences, Nursing, Healthcare, or a related scientific field. 2+ years of clinical monitoring experience within a pharmaceutical, biotechnology, CRO, or clinical research environment. Experience supporting studies in Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, Ophthalmology, or other related therapeutic areas. Experience in all therapeutic areas is not required. Working knowledge of EDC platforms, CTMS applications, and clinical trial technologies. Strong understanding of ICH-GCP guidelines, regulatory requirements, and clinical research best practices with excellent communication and organizational skills. Compensation: of the Clinical Research Associate (CRA): Salary Range: $100,000 - $140,000 dependent on experience Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K This job opens for applications on 9/4/26. Applications for this job will be accepted for at least 30 days from the posting date. #LI-HB1