Senior Medical Writer, Evidence Analyst

This is a fully remote position, open to applicants in India.

📋 Description

• Independently author and review regulatory and other medical writing deliverables, or collaborate with other Senior Medical Writers.

• Provide support to fellow writers in creating manuscripts, slide sets, abstracts, posters, and other techno-commercial documents as required.

• Responsible for authoring and reviewing patient narratives, Clinical Study Reports (CSRs), Protocols, Investigator Brochures (IB), and other regulatory submission documents.

• Conduct independent authoring and review of manuscripts, abstracts, posters, evidence synthesis projects, and various techno-commercial documents.

• Perform quality control on the aforementioned deliverables.

• Demonstrate adaptability in terms of timelines and writing styles to meet client requirements and therapeutic area specifications across diverse domains.

⛳️ Requirements

• A PharmD, M. Pharm, PhD, MD, or a post-graduate degree in life sciences, medical, or paramedical fields.

• A minimum of 3-5 years of experience in medical writing or a demonstrated flair for writing with established academic credentials.

• A solid understanding of industry standards and global trends in drug development and the medical device sector.

• Highly skilled in MS Office and other software tools for authoring and managing data handling and interpretation.

• Basic familiarity with automation platforms and comfort in their usage.

🏝️ Benefits

• A commitment to excellence and maintaining high standards.

• A creative, flexible, and innovative team player.

• Good judgment with the capacity to make timely and sound decisions.