Clinical Research Associate
We are seeking a Clinical Research Associate (CRA) to support ongoing clinical trials. The CRA will be responsible for monitoring study sites, ensuring compliance with study protocols, regulatory requirements, and good clinical practices. This role requires strong organizational skills and attention to detail.
Responsibilities:
Monitor clinical trial sites to ensure adherence to study protocols, GCP, and regulatory requirements
Conduct site initiation, monitoring, and close-out visits
Verify source data and ensure accurate case report form (CRF) completion.
Maintain trial documentation and ensure timely reporting of study progress
Support site staff with study-related training and issue resolution
Ensure patient safety and data integrity throughout the study lifecycle
Skills & Experience:
Bachelor’s degree in life sciences, nursing, or related field
Experience in clinical research or monitoring preferred
Knowledge of ICH-GCP guidelines and regulatory requirements
Strong communication, organizational, and problem-solving skills
EEO Employer
We are an equal opportunity employer and comply with all applicable federal, state, and local fair employment practices laws. We strictly prohibit and do not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex, sexual orientation, gender (including gender identity and expression), marital or familial status, age, physical or mental disability, perceived disability, citizenship status, service in the uniformed services, genetic information, or any other characteristic protected under applicable federal, state, or local law. Applications from members of minority groups and women are encouraged.