Clinical Research Associate

Job Description

We are seeking a Clinical Research Associate to provide comprehensive support to study sites and clinical project teams involved in clinical research studies. As the primary point of contact for study sites, you will ensure adherence to protocols, standard operating procedures (SOPs), and all applicable guidelines and regulatory requirements. This role involves independently conducting site visits, updating trial management systems, and proactively communicating protocol issues to project teams. Coordination with timelines and support throughout the study lifecycle are essential.

Qualifications

1. Bachelor's degree or equivalent in business, scientific, or healthcare. 2. Minimum 2 years on-site monitoring experience; 1 year in oncology trials preferred. 3. Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint). 4. Customer service skills, flexibility, and teamwork. 5. Attention to detail and accuracy. 6. Fluency in English, both verbal and written. 7. Knowledge of the drug development process. 8. Willingness to travel (60-70%).

Benefits

- Health insurance - Retirement plans - Paid time off - Flexible work arrangements