Quality Assurance Specialist

1 week ago

ghaziabad, India beBeeClinical Full time

Job OverviewClinical Site Auditor ensures compliance and quality at Clinical Trial sites conducts site audits reviews documentation verifies adherence to protocols GCP GLP and regulatory requirements.Conducts audits of clinical research sites across phases I–IV.Reviews CRFs informed consent forms and regulatory documents.Identifies and reports audit findings recommends corrective actions.Supports site staff with compliance guidance and training.Prepares audit reports and follows up on CAPA implementation.Clinical Research or Quality Auditing certification ACRP SOCRA preferred.Experience auditing multi-center or global trials preferred.Frequent travel required; flexible schedule to accommodate site audits necessary.About the RoleThis position requires a high level of professionalism expertise and organizational skills.Audit experience in pharmaceutical medical device or biotechnology industries is beneficial.Prior experience working in a fast-paced environment would be advantageous.The ideal candidate will have excellent communication interpersonal and problem-solving skills.Skills & QualificationsTo succeed in this role you must possess:Strong analytical and critical thinking skills.Excellent written and verbal communication skills.Ability to work independently as well as part of a team.BenefitsWe offer a comprehensive benefits package including:Competitive salary and bonus structure.Opportunities for career advancement and professional growth.Comprehensive health insurance and retirement plans.

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    1 week ago

    ghaziabad, India beBeeQuality Full time

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    ghaziabad, India beBeeCompliance Full time

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    ghaziabad, India beBeeAnalytical Full time

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