Medical Writer

Job description
We are seeking a talented and dedicated Medical Writer to join our team. As a Medical Writer, you will play a crucial role in communicating complex medical and scientific information to various audiences, including healthcare professionals, patients, regulatory bodies, and the general public. Your primary responsibility will be to develop high-quality, accurate, and engaging content that adheres to scientific and regulatory guidelines.

• Responsibilities:
• Content Development: Create clear, concise, and scientifically accurate medical content, including but not limited to scientific articles, clinical trial reports, regulatory documents, educational materials, marketing collateral, and website content.
• Research and Analysis: Conduct comprehensive research on medical and scientific topics, staying updated with the latest advancements, clinical data, and regulatory guidelines. Analyze scientific data, clinical studies, and other relevant sources to gather information and support content development.
• Writing and Editing: Produce well-structured, grammatically correct, and error-free documents that effectively communicate complex medical information in a manner appropriate for the target audience. Ensure adherence to regulatory guidelines, company standards, and style guides.
• Collaboration: Collaborate closely with cross-functional teams, including medical professionals, researchers, regulatory experts, and marketing personnel, to gather insights, review content, and ensure accuracy, relevance, and scientific integrity.
• Review and Quality Assurance: Review and proofread medical content to ensure accuracy, consistency, and adherence to industry-specific terminology, standards, and guidelines. Perform quality checks to ensure compliance with regulatory requirements.
• Compliance and Regulatory Support: Stay updated with relevant regulatory guidelines, such as FDA, EMA, and ICH guidelines, to ensure compliance in all medical writing activities. Provide support in the preparation and submission of regulatory documents.
• Client and Stakeholder Interaction: Interact with clients, healthcare professionals, and other stakeholders to understand project requirements, address queries, and incorporate feedback into content development.
• Documentation Management: Maintain organized records of reference materials, literature, and source documents used in content development. Ensure proper version control and documentation management for all deliverables.

Qualifications:

• Bachelors or advanced degree in life sciences, pharmacy, medicine, or a related field.
• Proven experience as a Medical Writer in a pharmaceutical, biotechnology, or healthcare setting.
• Excellent writing and communication skills, with the ability to distill complex scientific information into clear and concise content.
• Strong knowledge of medical terminology, clinical research methodologies, and regulatory guidelines.
• Familiarity with scientific databases, literature search tools, and citation management software.
• Proficiency in interpreting and presenting scientific data and clinical trial results.
• Attention to detail, with a strong commitment to accuracy, scientific integrity, and quality.
• Ability to work independently, manage multiple projects simultaneously, and meet tight deadlines.
• Proficient in using MS Office Suite (Word, Excel, PowerPoint) and other relevant software applications.
• Knowledge of medical writing guidelines (e.g., ICH-GCP, AMA style) and familiarity with common regulatory document templates (e.g., clinical study protocols, investigator brochures, clinical study reports)

Role: Medical Writer
Industry Type: Advertising & Marketing
Department: Research & Development
Employment Type: Full Time, Permanent
Role Category: Pharmaceutical & Biotechnology
Education
UG: Any Graduate
PG: Any Postgraduate