Clinical Trial Manager — Biotech Study Leader

Adicet Bio, Inc; Redwood City (CA); On-site; USD 131,000 - 181,000; Full time

Benefits offered by this job

Health plans

401(k) with company match

Employee stock purchase plan (ESPP)

Paid time off

Onsite gym and shuttle

Free lunches

Job summary

Adicet Bio, Inc. in Redwood City is seeking a Clinical Trial Manager to lead operational planning and delivery for assigned trials, ensuring GCP/ICH compliance and adherence to SOPs.

You will collaborate with study sites, CROs, and internal teams; oversee timelines and budgets; manage TMF and enrollment tracking. The role requires a BS or higher in science or nursing and at least 4 years in clinical research, with strong communication and vendor management skills.

Qualifications

• Excellent communication skills and ability to achieve milestones in a team environment.
• Strong working knowledge of FDA, ICH Guidelines, and GCPs governing the conduct of clinical trials.
• Experience with managing studies in electronic data capture systems.
• Experience with project, vendor, contract, and clinical research staff management.
• Experience with Institutional Review Board (IRB) preparations and submission.

Responsibilities

• Work closely with the Clinical Operations team to support all aspects of global clinical studies.
• Take a leadership role in site and study management activities including ICFs, site activations, monitoring reports, and study plan review.

Skills

Communication skills

Team collaboration

GCP/ICH knowledge

EDC experience

Education

BS or higher in science or nursing

Tools

Electronic data capture systems

Job description

Adicet Bio, Inc. in Redwood City is seeking a Clinical Trial Manager to lead operational planning and delivery for assigned trials, ensuring GCP/ICH compliance and adherence to SOPs.

You will collaborate with study sites, CROs, and internal teams; oversee timelines and budgets; manage TMF and enrollment tracking. The role requires a BS or higher in science or nursing and at least 4 years in clinical research, with strong communication and vendor management skills.