8 Icmje Guidelines Jobs

You will be responsible for the following key tasks: - Developing, writing, and editing scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Preparing regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Creating medical communication materials like slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborating with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conducting literature reviews and ensuring referencing accuracy using platforms l...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Th...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Th...

Red Nucleus is hiring a Scientific Director to join our global team! This role can be full-time remote in the US or Canada. Our purpose is advancing knowledge to improve lives. We succeed by being the premier provider of strategic learning and development, scientific advisory services, and medical communications solutions for the life sciences industry. Our global team is composed of nearly 1000 full-time employees whose commitment to creativity, quality, and on-time delivery is unrivaled in our space. At Red Nucleus, we believe in providing a rich working environment that pushes us to innovate in ways that engages our employees to be their best selves. Our culture is about meaningful work, ...

Role Overview: As an Associate Scientific Director at Red Nucleus, you will be a key member of the Medical Communications team. Your role will involve leading scientific accounts, providing high-quality editorial review, and acting as a scientific and therapeutic expert for assigned project teams. You will set standards for content development, mentor medical writing staff, and support business development efforts. Key Responsibilities: - Set standards for the assigned team to drive continuous improvement in quality and client interactions - Evaluate internal processes related to content development and suggest improvements - Ensure high-quality outputs from the scientific team - Identify tr...

You will be responsible for the following key tasks: - Develop, write, and edit various scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Prepare regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Create medical communication materials including slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborate effectively with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conduct thorough literature reviews and ensure precise referencing usi...

Site Name: Bengaluru Luxor North Tower Posted Date: Sep 19 2025 Key Responsibilities In partnership with the relevant publication planning teams, assure successful management of GSK's publication delivery. Provide end-to-end publications coordination and project management support (excluding writing support) to specific publication deliverables (including but not limited to manuscripts, abstracts, posters, presentations, publication enhancements, etc.) by closely collaborating with authoring teams, cross-functional teams of experts, and Publications Leads across TAs in alignment with asset Strategic/Tactical Publication Plans Ensure delivery of impactful, high-quality publications in a timel...

As the Lead Medical Writer at Tatvacare, you will be responsible for developing and reviewing high-quality medical content, including scientific publications such as original research articles, consensus reports, review articles, and clinical trial documentation. Your role will involve collaborating with cross-functional teams, providing scientific expertise, and ensuring compliance with regulatory and industry standards. The ideal candidate for this position will have extensive experience in medical writing, particularly in clinical development, regulatory affairs, and digital health research. Your key responsibilities will include developing and finalizing medical writing documents, coordi...