GCP Compliance Specialist CLIN BIOSCIENCES
CLIN BIOSCIENCES
Office Location
Full Time
Experience: 2 - 2 years required
Pay: INR 2400000 - INR 3600000 /year
Type: Full Time
Location: United Arab Emirates
Skills: clinicalqa, clinicalresearchuae, gcpcompliancespecialist, clinicaltrialsuae, complianceofficeruae
About CLIN BIOSCIENCES
Job Description
Roles and Responsibilities;
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Conduct GCP audits (internal and external) across clinical trial sites, vendors, and CROs.
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Ensure clinical trial documentation, processes, and practices meet GCP, ICH, and DHA/MOH/GCC regulatory standards.
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Prepare trial sites and teams for regulatory inspections .
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Investigate and document non-compliance, deviations.
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Collaborate with QA, clinical operations, and regulatory teams to enhance quality systems.
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Support training and awareness programs on GCP and compliance practices.
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Maintain audit reports, SOPs, risk logs, and inspection follow-ups.
Eligibility / Qualifications:
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Bachelors or Masters in Life Sciences / Pharmacy / Medicine / Clinical Research
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Certification in ICH-GCP, Quality Management Systems (QMS) or GCP Auditing preferred
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Understanding of clinical trial phases, regulatory pathways, and QA/QC systems
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Familiarity with UAE and GCC regulations is a strong advantage
Interested to apply can share you CV in Whatsapp/Call to 9342735755