Clinical Study Manager

About the role

Clinical Study Manager oversees the planning, execution, and regulatory compliance of clinical trials for medical devices.

Responsibilities

• Design study protocols, manage project schedules, and track data timelines.
• Supervise clinical site monitoring activities, recruitment, and retention strategies.
• Partner with research and development, biostatistics, regulatory affairs, and medical affairs teams.
• Manage trial budgets, negotiate contracts, and ensure adherence to Good Clinical Practice (GCP) standards.

Skills

• Clinical trial
• Clinical study
• Clinical research
• Project management
• Clinical trial management
• Clinical operation
• Diabetes
• Medical device

Additional Skills & Qualifications

• Medical device experience preferred.
• Experience with diabetes therapy is a plus.
• Ability to execute under FDA regulations 21 CFR Part 812 and related requirements.
• Available to work Pacific Time Zone hours (or PST hours).
• Expert level experience.

Pay

The pay range for this position is $50.00 – $70.00 per hour. Compensation within this range depends on qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent factors.

Benefits

• Medical, dental, and vision coverage
• Critical Illness, Accident, and Hospital insurance
• 401(k) retirement plan – pre‑tax and Roth post‑tax contributions
• Life Insurance (voluntary life & AD&D for employee and dependents)
• Short and long‑term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time off/leave (PTO, vacation, or sick leave)

Schedule

Work hours aligned with Pacific Standard Time (PST).

Location

Contract position based out of Los Angeles, CA. Fully remote.