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Role & Responsibilities
• Perform data QC and editing for regulatory documents, including Clinical Study Reports (CSR), Investigator’s Brochures (IB), Protocols, and more
• Ensure adherence to ICH-GCP guidelines and internal quality standards
• Collaborate with CROs and sponsor companies to deliver high-quality outputs
Qualification
• Strong experience in medical editing and QC for regulatory documents
Experience
• Experience in clinical research or pharmaceutical industries
• Familiarity with regulatory documents and editing processes
Skills
• Excellent written and verbal communication skills
• Ability to manage multiple projects under tight timelines
• Attention to detail and strong understanding of clinical research processes
Preferred Skills
• Familiarity with publishing tools and regulatory submission platforms
About the Company
• Syneos Health is a global, full-service biopharmaceutical solutions organization committed to advancing clinical research for pharmaceutical and biotechnology companies worldwide.