We are seeking a Sr. Clinical Trial Associate with experience supporting clinical trials, study coordination, and clinical operations.

Responsibilities:
• Maintain Trial Master Files (TMF)
• Support IRB submissions and study documentation
• Coordinate clinical trial activities and site communications
• Perform CTMS data entry and tracking
• Support investigator meetings and study start-up activities
• Track monitoring reports and clinical supplies

Requirements:
• Clinical research / clinical trial experience
• Experience with TMF, CTMS, IRB submissions, and study tracking
• Knowledge of GCP / ICH guidelines
• Strong organizational and communication skills
• CRO, biotech, pharma, or healthcare research background preferred

Ideal backgrounds:
• Clinical Trial Associate (CTA)
• Clinical Research Coordinator
• Clinical Operations Coordinator
• TMF / Regulatory Coordinator

Apply today or reach out for more information.

Ascendo is a certified minority owned staffing firm, and we welcome and celebrate diversity. Ascendo is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, parental status, military service or any other characteristic protected by federal, state or local law.

Contact information

George Martinez