Clinical Trial Associate, Clinical Operations - Remote

Overview

The Clinical Trials Associate (CTA) is an integral part of the study team providing project system, tracking, and administrative support throughout all phases of clinical studies, ensuring compliance and effective communication among stakeholders.

In Short

• Support clinical study activities from start-up to close-out.
• Maintain and manage the Trial Master File (TMF).
• Organize study team SharePoint sites and trackers.
• Track essential documents for studies and sites.
• Coordinate study execution team meetings.
• Communicate effectively with stakeholders.
• Participate in audits and inspections.
• Manage vendor and site contract tracking.
• Up to 10% travel required.
• 1-2 years clinical trial experience preferred.

Requirements

• Bachelor’s degree in life sciences or related field.
• Proactive communication skills.
• Strong organizational abilities.
• Ability to manage multiple projects under tight deadlines.
• High energy level and positive attitude.
• Hands-on and action-oriented.
• Experience with ICH-GCP compliance.
• Familiarity with electronic document management.
• Effective under stress.
• Ability to lift/move up to 15 pounds.

Benefits

• Medical, dental, and vision care.
• 401(K) and financial protection benefits.
• Paid vacation and holidays.
• Flexible work-life programs.
• Tuition reimbursement.
• Employee assistance programs.
• Recognition programs.
• Parental and caregiver leave.
• Support for family care services.
• Wellbeing support programs.