Clinical Trials Lead, Study Operations

Neurocrine Biosciences; San Diego (CA); On-site; USD 111,000 - 151,000; Full time

Benefits offered by this job

Annual bonus

Equity program

Health benefits

Retirement plan

Job summary

Neurocrine Biosciences is seeking a Clinical Trials professional to lead operational activities for planning, initiation, conduct and close-out of assigned studies (domestic and global). You will work with CTMs, CROs, and CSPs to ensure studies run in compliance with FDA regulations and ICH guidelines.

The role emphasizes project management, data analysis, and collaboration across functional teams, with responsibilities for timelines, monitoring plans, and recruitment support.

Qualifications

• BS/BA in a scientific field with 4+ years of clinical trials or operations experience.
• Master’s degree in a scientific field with 2+ years of related experience.

Responsibilities

• Partner CTMs to ensure FDA/ICH/GXP compliance across studies.
• Lead on smaller studies or contribute as team member.
• Develop reports and provide insights for study design discussions.
• Manage project plans, metrics, and CRO/CSP performance for assigned studies.
• Participate in study team meetings and assist with recruitment efforts.

Skills

Clinical trials

CRO management

FDA regulations

ICH guidelines

Project management

Data analysis

Cross-functional

Communication

Education

BS/BA in science

Master’s in science

Tools

None

Job description

Neurocrine Biosciences is seeking a Clinical Trials professional to lead operational activities for planning, initiation, conduct and close-out of assigned studies (domestic and global). You will work with CTMs, CROs, and CSPs to ensure studies run in compliance with FDA regulations and ICH guidelines.

The role emphasizes project management, data analysis, and collaboration across functional teams, with responsibilities for timelines, monitoring plans, and recruitment support.