Associate Clinical Study Manager (San Antonio, Tx)
Worldwide Clinical Trials · San Antonio, TX
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Associate Clinical Study Manager will coordinate site-level monitoring activities for Phase I-IV clinical trials, supporting the Clinical Study Manager with technical, financial, and operational aspects. The role involves managing study visits, maintaining documentation, coordinating training, and facilitating sample shipments.
What they're looking for
- Bachelor's degree in life sciences or health field
- Or associate's degree with 2+ years clinical research experience
- Or 4+ years clinical research experience without degree
- Excellent communication, planning, and organizational skills
- Strong problem-solving and independent work capabilities
- Customer service and client negotiation proficiency
What you'll be doing
- Coordinate study monitoring visits including system access, space reservation, and document preparation
- Collaborate with clinic departments to resolve queries and action items promptly
- Manage and file clinical approval forms, training documentation, and signature forms
- Ensure staff training compliance with GCP standards, SOPs, and applicable regulations
- Facilitate bioanalytical sample shipments according to study timeline and client requests
Compensation$19.95 - $39.66 hourly
Privacy & handoff
This role links to Worldwide Clinical Trials's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.