3 Reference Management Jobs

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, coordinating publication of scientific data in peer-reviewed journals, leading the writing process to ensure timely completion of deliverables, and providing guidance to the team in the review and writing of scientific documents. You will also be involved in continuous improvement initiatives, training and mentoring the medical writing team, and ensuring compliance with journal and regulatory guidelines. To excel in this role, you should have an advanced degree in a life sciences discipline, experience in writing scientific publications, and strong communication and interpersonal skills. Additionally, you should have at least 5 years of experience in medical and scientific writing within pharmaceutical, healthcare, CRO, or digital health domains, proficiency in statistical interpretation, and expertise in real-world evidence research and systematic reviews. In terms of technical proficiency, you should be adept in using Microsoft Office Suite, reference management tools such as EndNote and Mendeley, and statistical analysis software like SPSS and SAS. Familiarity with compliance guidelines such as ICMJE, CONSORT, PRISMA, and GPP, as well as ethical considerations related to authorship and conflicts of interest, will be an advantage. This is a full-time position that offers benefits including health insurance, paid sick time, and provident fund. The work schedule is during the day shift, and the work location is in person. If you possess strong leadership, strategic thinking, and mentorship abilities, along with excellent communication and stakeholder management skills, we encourage you to apply for this exciting opportunity at Tatvacare.,

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 HEOR project types such as RWE claims, budget impact models, and value communication activities. Proficiency in reference management software, strong attention to detail, and organizational skills are essential for this role. You will collaborate with team members and stakeholders across Trinity locations to ensure high-quality deliverables and provide strategic recommendations to clients. Your responsibilities will also include creating client-ready materials, supporting business development through project proposals, and contributing to the growth of the EVAP function through internal initiatives focused on professional development. To qualify for this position, you should have a Bachelor's degree in Pharmacy, Biology, Chemistry, or related fields, with a Master's or PhD preferred. Experience in conducting systematic literature reviews, proficiency in literature databases and search tools, strong analytical and critical thinking skills, and excellent written and verbal communication skills are required. You should also have the ability to work independently and collaboratively in a team environment and a proven track record of relevant publication support or authorship. Specific skills that will be valuable in this role include advanced research skills, data extraction and synthesis, critical appraisal of literature, and report writing and presentation skills. By joining Trinity's vibrant and growing Evidence Strategy / HEOR team, you will have the opportunity to take on challenging and rewarding roles that drive client success using HEOR and Market Access expertise.,

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 compelling and compliant medical writing materials. You will be expected to adhere to client and regulatory guidelines, such as ICH, FDA, and EMA, while ensuring consistency, accuracy, and scientific integrity in all documents. As a Medical Writer, you will review and revise content based on feedback from reviewers and editors, manage multiple writing projects simultaneously while meeting strict deadlines and quality standards, and support quality control and peer-review processes to ensure excellence in medical documentation. Requirements for this role include a Bachelor's, Master's, or Doctorate degree in Life Sciences, Medicine, Pharmacy, or a related field, along with at least 3 years of experience in medical writing within the pharmaceutical, healthcare, or life sciences industries. A strong understanding of medical and scientific terminology, clinical research processes, and regulatory requirements is crucial. Additionally, excellent writing, editing, and verbal communication skills are necessary, with an eye for detail. Experience in preparing clinical and regulatory documents, publications, and scientific communications is preferred. You should be able to interpret and summarize complex scientific data for different audiences and possess familiarity with industry guidelines such as ICH, GCP, AMA, FDA, and EMA. Proficiency in Microsoft Office Suite and reference management tools is required, along with strong organizational skills, multitasking abilities, and the capacity to work independently under tight deadlines. Moreover, experience collaborating with cross-functional teams, including researchers, medical professionals, and regulatory experts, will be beneficial in this role. Join RRD GO CreativeTM, a company with over three decades of experience in business communications, marketing solutions, and digital productivity solutions. Our expertise in Global Brand Solutions, Smart Work Solutions, and Technology & Innovation Services enables us to transform the way businesses interact with customers, fostering strong brand loyalty. Our team of 8,000 experts across 42 locations collaborates across various industries to co-create a future-ready business landscape. We work with businesses to digitize every aspect of the Customer Journey, translating strategic visions of expansion and efficiency into superior Customer Experiences. Let us help you address customer needs effectively and make Customer Experience your competitive differentiator.,