Senior Regulatory Document Specialist

2 days ago


jaipur, India beBeeMedical Full time

Regulatory Medical WriterThis role involves drafting, reviewing and finalizing regulatory documents such as clinical study reports, investigator brochures and other essential documents.Key Responsibilities:Drafting and reviewing regulatory documentsPerforming literature reviewsCollaborating with cross-functional teamsEnsuring regulatory complianceRequirements:Proficiency in medical writingFamiliarity with regulatory document preparationStrong understanding of clinical study designs and regulatory guidelinesExcellent organizational skillsAdvanced proficiency in Microsoft Office SuiteAdvanced degree in life sciences or a related fieldThe ideal candidate will work closely with stakeholders to meet project deadlines and regulatory compliance standards. This is a full-time remote role that requires a strong understanding of clinical study designs, statistical principles and regulatory guidelines such as ICH-GCP and FDA/EMA standards.



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