6 Reference Management Jobs

As a Junior Editor at our company, you will play a crucial role in the editorial process. Your responsibilities will include: - Reviewing, editing, and proofreading manuscripts to ensure linguistic accuracy, structural coherence, and adherence to style guidelines. - Collaborating with authors, senior editors, and production teams to maintain the quality, consistency, and integrity of published content. - Having a good command of English with strong editing and proofreading skills. You can be trained if needed. - Possessing a Bachelor's degree in Science (Masters preferred). - Demonstrating familiarity with academic publishing or content management workflows as an advantage. - Proficiency in ...

Role Overview: As a Medical Writer at RRD GO Creative, you will be responsible for developing high-quality and scientifically accurate medical and regulatory documents, including clinical study reports, protocols, and brochures. Your role involves creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards is essential. Collaboration with subject matter experts, scientists, and regulatory teams is crucial to develop compelling and compliant medical writing materials. You will also need to adhere to client a...

Role Overview: As a Global Systematic Literature Review (SLR) Senior Associate in the Global Health Economics & Outcomes Research (HEOR) department at Amgen, your primary responsibility is to provide expertise in designing, executing, and managing literature review services. You will collaborate closely with the team lead and Global HEOR Product Leads to align with HEOR product strategy. Your role is crucial in supporting global access to Amgen's therapies by generating high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities: - Refine literature review questions in alignment with the team lead and prepare research protocols. - Design literature searches for el...

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...

You are a passionate and intellectually curious health economics and outcomes research (HEOR) research specialist looking to join Trinity's Evidence Strategy / HEOR team. In this role, you will provide strategic and tactical support to biotech, pharma, and medical device clients in evidence planning, value creation, and scientific communication through real-world HEOR. As a Consultant located in Gurgaon, India, you will be responsible for conducting systematic literature reviews using PRISMA guidelines, developing search strategies, screening and selecting studies, extracting and synthesizing data, and analyzing findings to draw evidence-based insights. Additionally, you will work on various...

RRD GO Creative is seeking experienced Medical Writers to join our team in Chennai. In this role, you will play a crucial part in developing high-quality and scientifically accurate medical and regulatory documents, such as clinical study reports, protocols, and brochures. Your responsibilities will also include creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. To excel in this role, you must conduct thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams is essential to develop compelli...