Clinical Trials Specialist – Start-Up & IRB Support

Neurocrine Biosciences; Greater London; On-site; GBP 42,000 - 54,000; Full time

Job summary

Neurocrine Biosciences in the United Kingdom is seeking a detail-oriented Clinical Trials Operations Professional to support planning, initiation, conduct and close-out of assigned clinical studies. You will work with CTMs, CROs and investigator sites to ensure trials conform to GCP, FDA/EU requirements and robust data integrity.

Key tasks include managing essential document collection, IRB/IEC submissions, study timelines, site monitoring support, and maintaining eTMF quality.

Qualifications

• BS/BA in scientific field with 2+ years of clinical trials or operations experience.
• Master's in scientific field with some clinical trials experience.
• Knowledge of ICH, GCP, FDA regulations, and EU Directive.
• Experience in clinical operations from start-up to close-out.
• Some trial management protocol and process knowledge.
• Ability to plan activities and adapt to changing circumstances.
• Ability to meet multiple deadlines with accuracy.

Responsibilities

• Coordinate IRB/IEC submissions and approvals from start-up to closeout.
• Collaborate with CTMs, CROs, and investigator sites to run trials per GCP.
• Prepare data for technical and study design discussions.
• Provide administrative support including invoices and tracking metrics.
• Develop study timelines aligned with corporate goals.
• Support recruitment efforts and site monitoring activities.
• Maintain organized eTMF documents and QA checks.

Skills

Strong computer skills

Communication skills

Problem solving

Analytical thinking

Time management

Team player

Project management

Education

Bachelor's degree in scientific field

Master's degree in scientific field

Job description

Neurocrine Biosciences in the United Kingdom is seeking a detail-oriented Clinical Trials Operations Professional to support planning, initiation, conduct and close-out of assigned clinical studies. You will work with CTMs, CROs and investigator sites to ensure trials conform to GCP, FDA/EU requirements and robust data integrity.

Key tasks include managing essential document collection, IRB/IEC submissions, study timelines, site monitoring support, and maintaining eTMF quality.