Syneos Health
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
Senior Medical Editor
🔥 0 minutes ago
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Syneos Health
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
📋 Description
• Perform QC review of documents (eg, clinical study protocols and amendments, clinical study reports [CSRs], Investigator's Brochures, and Module 2 clinical summary documents) to ensure compliance with the client Style Guide and submission standards • Verify data in documents against the source tables, figures, and listings and format tables according to the client standards • Copyedit/proofread clinical documents for grammar, style, and formatting according to AMA and the client style guides • Ensure internal consistency and confirm that data are reported correctly, statements accurately reflect source documents or data (eg, SAS tables and listings) • Check reference list in documents, including verifying citation information vs PubMed, ordering copies of references and adding to the electronic document management system (EDMS), and ensuring each reference is cross-referenced in the document • Proofread documents against the standard templates to ensure compliance with required sections and text • Perform publishing of nonclinical and clinical documents and the compilation of required CSR appendices, as needed • Lead and actively participate in process improvement initiatives and assist Medical Writing staff with other tasks, as appropriate • May oversee the workload for the editors, establishing schedules and interacting with cross-functional authors • Assist with training of more junior editors or contract staff
🎯 Requirements
• Bachelor’s degree in English, Basic Science, Business, or other analytical field with 4 years related experience in the pharmaceutical industry OR 8+ years of experience in a discipline directly related to document production (eg, medical writing, QC, editing, publishing) • Strong working knowledge of the editorial and publishing activities within Clinical Development • Proficient in Microsoft Word, including the ability to format tables, insert cross-references, apply styles, and use templates • Experience with PowerPoint, Excel, Visio, Adobe • Strong working knowledge of Adobe PDF bookmarking and internal/external hyperlinking to meet submission-ready standards • Experience in the use of an EDMS (eg, Veeva Vault or SharePoint) • Ability to effectively communicate with vendors and manage outsourced editorial work • Keen attention to detail • High level of English
🏖️ Benefits
• We are passionate about developing our people, through career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Committed to building an inclusive culture
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