Regional GCP Compliance Director – Oncology Trials

BeiGene; Indiana; Hybrid; USD 130,000 - 180,000; Full time

Job summary

A leading biotechnology firm is seeking a Regional Clinical Compliance Director/Senior Director in Indiana. The successful candidate will oversee clinical compliance and lead initiatives to ensure GCP adherence in oncology global trials. With a strong background in regulatory standards and 14+ years of experience, this role is crucial for ensuring inspection readiness and compliance at various operational levels. Strong leadership, analytical skills, and effective communication in a multicultural setting are essential for success in this position.

Qualifications

• Minimum 14 years of progressive experience in clinical operations roles.
• Experience in GCP compliance or quality-related roles.
• Experience in oncology global trials is preferred.

Responsibilities

• Implement Global Clinical Compliance strategy.
• Provide compliance oversight and quality support to study teams.
• Identify and resolve potential compliance matters.

Skills

GCP expertise

Analytical skills

Project management

Leadership

Communication skills

Education

Bachelor’s degree in scientific, medical or healthcare discipline

Job description

A leading biotechnology firm is seeking a Regional Clinical Compliance Director/Senior Director in Indiana. The successful candidate will oversee clinical compliance and lead initiatives to ensure GCP adherence in oncology global trials. With a strong background in regulatory standards and 14+ years of experience, this role is crucial for ensuring inspection readiness and compliance at various operational levels. Strong leadership, analytical skills, and effective communication in a multicultural setting are essential for success in this position.