What are the responsibilities and job description for the GCP/GVP QA Director position at RG&T Solutions?
The GCP/GVP QA Director oversees compliance with Good Clinical Practices and Good Pharmacovigilance Practices, ensuring quality is integrated into all clinical research processes.
They develop and implement QA strategies, support audits and regulatory inspections, and manage key metrics to track compliance and data integrity.
The role involves collaborating with clinical development teams, providing guidance on regulatory requirements, and supporting internal staff and external consultants.
Candidates should have extensive experience in pharmaceutical/biotech industries, with expertise in GCP/GVP audit management, drug development processes, and global regulatory standards.
Strong communication, problem-solving skills, and the ability to influence cross-functional teams are essential.
This onsite position requires travel (15-20%) and offers a competitive salary, comprehensive benefits, and growth opportunities.
It does not have supervisory responsibilities but demands high independent judgment and technical expertise.
They develop and implement QA strategies, support audits and regulatory inspections, and manage key metrics to track compliance and data integrity.
The role involves collaborating with clinical development teams, providing guidance on regulatory requirements, and supporting internal staff and external consultants.
Candidates should have extensive experience in pharmaceutical/biotech industries, with expertise in GCP/GVP audit management, drug development processes, and global regulatory standards.
Strong communication, problem-solving skills, and the ability to influence cross-functional teams are essential.
This onsite position requires travel (15-20%) and offers a competitive salary, comprehensive benefits, and growth opportunities.
It does not have supervisory responsibilities but demands high independent judgment and technical expertise.