Medical Writer (Remote)

About the role

The Medical Writer is responsible for evaluating medical literature, developing and editing clinical development documents, and managing project workflows with minimal supervision.

Responsibilities

• Write and edit clinical protocols, investigator's brochures, clinical study reports, consent forms, safety and efficacy summaries, and publication materials.
• Ensure timely completion of assignments, maintain workflow, and deliver high-quality documents adhering to client templates and style guides.
• Collaborate with clients and team members, take ownership of projects, and mentor junior staff.

Requirements

• Minimum 3-5 years of regulatory and clinical medical writing experience in the pharmaceutical industry.
• Degree in a scientific, medical, or clinical discipline (Bachelors, Masters, or Ph.D.).
• Proven experience leading clinical study protocols and managing teams with strict deadlines.
• Exceptional writing, organizational, and multitasking skills.
• Expertise in MS Word, Excel, PowerPoint; knowledge of regulatory regulations and guidelines is advantageous.
• Strong communication skills and ability to work independently are essential.