Sr. Medical Writer

Anacipher Cro; Hyderabad; On-site; INR 600,000 - 800,000; Full time

Job summary

Anacipher Cro is seeking a skilled medical writer to manage and deliver complex medical writing projects from concept to completion, ensuring accuracy and regulatory compliance across diverse audiences including clinicians and researchers.

The role requires strong editing, literature review, and communication skills, with the ability to work independently within cross-functional teams and adhere to regulatory standards and internal templates.

Qualifications

• Strong understanding of medical terminology, anatomy, physiology, pharmacology, and medical devices.
• Excellent writing, editing, and communication skills; adapt tone and style to audience.
• Ability to work independently and collaboratively with strong attention to detail.
• Proficiency in Word, PowerPoint, Excel, and Adobe Creative Suite.
• Familiarity with regulatory requirements governing medical device submissions, including FDA and ICH guidelines.
• Strong analytical and problem-solving skills with the ability to analyze data sets.

Responsibilities

• Develop and maintain complex medical writing projects from concept to completion; ensure accuracy and regulatory compliance.
• Collaborate with cross-functional teams to integrate medical writing into project objectives.
• Conduct thorough research of medical literature to stay updated on industry trends.
• Create engaging content for clinicians, researchers, and stakeholders with clear language.
• Edit and review medical documents for accuracy and adherence to style guides.
• Participate in quality control processes to ensure regulatory standards and internal guidelines compliance.

Skills

Medical writing

Cross-functional collaboration

Literature review

Editing

Quality assurance

Content creation

Tools

MS Word

PowerPoint

Excel

Adobe Creative Suite

Job description

• Develop and maintain complex medical writing projects from concept to completion, ensuring accuracy, clarity, and consistency with regulatory requirements.
• Collaborate with cross-functional teams, including clinical operations, data management, and project management, to ensure seamless integration of medical writing activities into overall project objectives.
• Conduct thorough research and analysis of medical literature to stay updated on industry trends, best practices, and emerging developments.
• Create engaging and informative content for various audiences, including clinicians, researchers, and stakeholders, using clear and concise language.
• Edit and review medical documents for accuracy, grammar, punctuation, spelling, and adherence to style guides and templates.
• Participate in quality control processes to ensure compliance with regulatory standards and internal quality guidelines.

Job Requirements

• Strong understanding of medical terminology, anatomy, physiology, pharmacology, and medical devices.
• Excellent writing, editing, and communication skills, with the ability to adapt tone and style according to audience needs.
• Ability to work independently and collaboratively as part of a team, demonstrating strong attention to detail and organizational skills.
• Proficiency in using authoring tools such as Word, PowerPoint, Excel, and Adobe Creative Suite.
• Familiarity with regulatory requirements governing medical device submissions, including FDA regulations and ICH guidelines.
• Strong analytical and problem-solving skills, with the ability to analyze complex data sets and draw meaningful conclusions.