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Hiring Compliance Manager or QA manager with extensive experience in Clinical research and managing the entire compliance/QA department of CRO or Pharma

*At least 4 to 5 years’ experience in a similar role in a Clinical Research Organization or Pharmaceutical business.
*Expert working knowledge of GCP guidelines and quality regulations/expectations pertaining to clinical trials.
*Knowledge of maintaining and improving quality systems and procedures.
*Prior experience in a Quality role with knowledge of performing Quality checks or audits of data.
*Exposure to client audits and regulatory inspections, ideally in a Quality role.
*A demonstrated commitment to quality in a regulated environment.
*Ability to work independently, with minimal supervision, and be confident to make decisions and escalate accordingly.
*Exceptional customer services skills to both internal and external stakeholders.
*Proven clinical trials project management experience
*Life science or other relevant degree

You can share resume with divya@tech-observer.com

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