Clinical Research Regulatory Administrator

Job Summary

A company is looking for an Independent Contractor - Clinical Research Regulatory and Ops Admin.

Key Responsibilities:

• Provide regulatory leadership to ensure compliance with ICH and GCP standards across multiple clinical trial locations
• Train and oversee the development of new staff to support clinical trial operations
• Lead the study start-up process, managing regulatory documents and ensuring timely launches of studies

Required Qualifications:

• Bachelor's degree in Life Sciences, Healthcare, Regulatory Affairs, or a related field
• Extensive experience in research administration, clinical trial management, and regulatory management
• In-depth knowledge of ICH guidelines and GCP regulations
• Proven track record in leading successful study start-ups and maintaining compliance
• Experience in training and mentoring staff for their professional growth