GCP Auditor - Global R&D Audit

Ladders; United States; Remote; USD 105,000 - 142,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Retirement plan

Flexible spending accounts

Discretionary annual bonus

Job summary

Ladders is seeking a GCP Auditor to join our client’s team in the Pharmaceuticals & Biotech space. This remote US-based role focuses on planning, conducting, and reporting Good Clinical Practice audits across a global R&D environment, and often serves as lead auditor on complex audits.

The role collaborates with management and cross-functional stakeholders to identify risks, support regulatory readiness, and strengthen quality systems, with participation in inspections and process improvements

Qualifications

• Experience in Good Clinical Practice auditing or as regulatory inspector.
• Strong knowledge of GCP standards and audit processes.
• Postgraduate qualification is preferred.

Responsibilities

• Plan, conduct, and report GCP compliance audits worldwide.
• Serve as lead auditor for complex GCP audits.
• Identify and communicate compliance risks to management.
• Participate in regulatory authority inspections.
• Contribute to or lead process-improvement initiatives.
• Develop controlled documents for R&D quality.

Skills

GCP auditing

Regulatory inspections

Auditing processes

Education

Doctorate OR Master's +2 years OR Bachelor's +4 years OR Associate +8 years OR HS diploma +10 years

Job description

For our client, we are seeking a GCP Auditor - Global R&D Audit to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will focus on planning, conducting, and reporting Good Clinical Practice compliance audits across a global R&D environment. The position will also serve as a lead auditor on complex audits, partnering with management and cross-functional stakeholders to identify risks, support regulatory readiness, and strengthen quality systems.

In addition, the auditor will participate in regulatory authority inspections and help drive process improvements that enhance audit effectiveness and operational compliance.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $104,725 – $141,686 annually

Responsibilities

• Plan, conduct, and report Good Clinical Practice compliance audits worldwide
• Serve as lead auditor for complex GCP audits
• Identify and communicate compliance risks to management
• Participate in regulatory authority inspections
• Contribute to or lead process improvement initiatives
• Develop controlled documents for R&D quality

Qualifications

• Doctorate degree in a relevant field, or Master's degree plus 2 years of relevant experience, or Bachelor's degree plus 4 years of relevant experience, or Associate's degree plus 8 years of relevant experience, or High school diploma/GED plus 10 years of relevant experience
• Postgraduate qualification preferred
• Extensive experience in GCP auditing or as a regulatory inspector
• Strong knowledge of Good Clinical Practice standards and audit processes

Benefits

• Comprehensive medical, dental, and vision coverage
• Retirement and savings plan with company contributions
• Flexible spending accounts
• Discretionary annual bonus program
• Award-winning time-off plans
• Flexible work models where applicable

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.