Clinical Trial Manager

Part-time, onsite role in San Diego requiring local candidates (20–25 hours per week, 1–2 days onsite).

Responsibilities

• Serve as the study lead and/or provide study management support for complex Phase 1/2a cell therapy studies where needed; oversee enrollment, maintenance, and close-out to ensure timely delivery.
• Oversee aspects of study management to ensure execution accuracy and high-quality data for clinical studies.
• Oversee work performed by CROs, study vendors, and investigative sites taking full ownership of quality and timelines.
• Develop critical study documents, as needed (e.g., informed consent forms, management plans, study trackers).

Requirements

• Bachelor’s degree in a scientific or healthcare-related discipline with a minimum 6 years of hands-on clinical trial management experience, preferably in a pharmaceutical or biotech environment.
• A combination of CRO and pharma/biotech experience will be considered.
• Experience supporting pre-NDA programs and Phase 1 first-in-human clinical trials, including operational strategy, study oversight, monitoring, and close-out activities.

Pay

$75–85 per hour based on level and experience.