Regulatory Start-Up Lead for Multi-Site Clinical Trials

Barrington James; Oregon; On-site; USD 90,000 - 130,000; Full time

Job summary

Barrington James is seeking a regulatory start-up lead to own regulatory activities from study selection through site activation across multiple research sites. You will coordinate with business development and operations to keep study start-up on track and maintain inspection-ready files.

The role requires strategic, analytical thinking, excellent organization, and a track record of delivering high-quality work to deadlines, with clear communication to remote teams and cross-functional partners.

Qualifications

• Experience in regulatory or study start-up within a clinical research site network.
• Excellent organizational skills and attention to detail.
• Ability to meet deadlines with high-quality work.
• Strategic analytical thinking and data-informed decision making.
• Clear communication with remote, cross-functional teams.

Responsibilities

• Own regulatory submissions and documentation for new studies across multiple research sites.
• Coordinate with business development and operations to keep start-up on track.
• Maintain inspection-ready regulatory files.
• Identify risks and bottlenecks early and propose practical solutions.
• Help refine and improve start-up processes as the team scales.

Skills

Regulatory submissions

Study start-up

Cross-functional collaboration

Attention to detail

Independent working

Tools

eRegulatory systems

Job description

Barrington James is seeking a regulatory start-up lead to own regulatory activities from study selection through site activation across multiple research sites. You will coordinate with business development and operations to keep study start-up on track and maintain inspection-ready files.

The role requires strategic, analytical thinking, excellent organization, and a track record of delivering high-quality work to deadlines, with clear communication to remote teams and cross-functional partners.