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Sr Medical Editor

0-2 years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

πŸ“Œ Senior Medical Editor | Syneos Health
πŸ“ Location: India (Home-Based)
πŸš€ Leading Biopharmaceutical Solutions Organization

🌟 About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our work in clinical, medical affairs, and commercial sectors aims to provide impactful solutions for modern market realities. We place the customer and patient at the center of everything we do.

πŸ“ About the Role

The Senior Medical Editor will take the lead on ensuring medical documents meet sponsor and regulatory standards. The role involves project leadership, copyediting, data integrity reviews, and mentoring junior medical editors. You will work on complex writing projects, helping to guide internal teams and ensuring that documents adhere to the required style and regulatory standards.

πŸ” Key Responsibilities

Project Leadership & Management

βœ” Lead Projects: Oversee complex medical writing projects, coordinating timelines, budgets, and teams.
βœ” Mentorship & Training: Provide guidance and training to medical writers and editors on data integrity, editorial standards, and best practices.
βœ” Monitor Deliverables: Track project progress and keep relevant stakeholders informed of timelines and deliverable risks.

Editing & Data Review

βœ” Copyediting: Edit documents for grammar, style, punctuation, and consistency following AMA or custom guidelines.
βœ” Data Integrity: Review documents for accuracy, ensuring all data and content align with regulations.

Process Improvement

βœ” Develop Tools: Contribute to the improvement of editing processes, developing tools and updating policies for better efficiency.
βœ” Regulatory Compliance: Ensure all documents are in line with FDA, EU, and ICH guidelines.

πŸ“‹ Qualifications

πŸŽ“ Bachelor’s Degree in Life Sciences, Clinical Sciences, English, Journalism, or a related field.
πŸ“Œ Experience: Significant publishing experience, especially with Adobe Acrobat or ISIToolbox.
πŸ“Œ Skills: Proficiency in Microsoft Office Suite, attention to detail, copyediting, and data review.
πŸ“Œ Familiarity: Extensive knowledge of the AMA style guide, FDA, EU, and ICH regulations.

🌍 Why Syneos Health?

🌟 Career Growth: We offer development opportunities, technical training, and peer recognition.
🌍 Inclusive Culture: We celebrate diversity and create a workplace where everyone belongs.
πŸ’Ό Impact: Our team has contributed to 94% of FDA-approved drugs in the last 5 years.

πŸ“© Apply Now