Junior technical medical writer jobs in the Editorial & Writing category and Biotechnology & Pharmaceuticals industry

Job Summary: The purpose of this job is to create, without supervision, any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This position is for an independent, proactive, experienced medical writer with d...
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. Exciting Technical Writer job opportunity with a global industry leader! Adecco Engineering and Technical, a division of the world leader in the recruitment of professionals, has an immediate opening for an approximate 4+ month temporary role for a Technical Writer with a leading manufacturing company in the Mayfield/Highland Heights area, near Cleveland, OH. This is a great opportunity to gain ...
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Enterprise System Partners (ESP) is a global consulting and project engineering company with its European Headquarters in Ireland and its North American headquarters in Massachusetts. We have a wide portfolio of projects that we are actively involved in across Europe and the US and we always welcome applications from highly motivated people to help drive us forward. We are actively looking to recr...
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Principal Objective(s): The Principal Medical Writer researches, writes, and edits complex clinical documents for submission to regulatory agencies to meet the objectives of Clinical Research and Development (CRAD). Major Duties and Responsibilities: Preparation of clinical study reports, integrated summaries of safety and efficacy, and other high level clinical summary and overview documents for ...
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. This position is responsible for providing high quality clinical documentation to the Genzyme Rare Disease business. The purpose of this job is to create and to manage creation by others of any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data o...
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Global manufacturer seeking a technical writer to perform statistical analysis of trending data. Must be able to summarize technical data for formal protocols. Candidate will write and review regulatory compliance related documentation. Will be required to perform data entry in global software systems. Will organize materials and complete writing assignments based on set standards; maintaining rec...
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If you would like to combine your love of science with your writing skills in an intellectually stimulating environment that develops training materials for the pharmaceutical industry, we welcome your application for the role of Medical Writer I. In this role, you will have an opportunity to share your passion for science with other talented individuals who write training materials that cover all...
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If you thrive in an intellectually stimulating environment where you can utilize your extensive medical knowledge in writing training materials for the pharmaceutical, biotech, and device industries, we welcome your application for the role of Senior Medical Writer. In this role, you will have an opportunity to share your passion for science with other talented individuals who write training mater...
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Isis Pharmaceuticals, Inc., located in the North San Diego County city of Carlsbad, was founded in 1989 to create advanced, novel medicines to treat complex and challenging diseases. We are the pioneer in the discovery and development of antisense drugs with more than 1600 patents. Isis is a challenging, motivating and rewarding environment designed to foster innovation and scientific excellence. ...
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Technical Writer (TEMP) - Packaging & Manufacturing Bronx, NY The Technical Writer will prepare, edit and update controlled documents including standard operating procedures (SOP), On the Job Aids, Training Manuals and/or standard work instruction (SWI) documents for assigned areas and processes, ensuring documents accurately reflect correct procedures as determined by subject matter experts (SME)...
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. Adecco Engineering and Technical has an urgent need for a SR. Regulatory Specialist II Position in the Bay Area on a Contract -to-hire basis. Are you a great Medical Writer/ Editor? Are you looking to challenge the skills you already have? Then is is the opportunity for you with the wold's leading Biotech/Pharmaceutical Company located in Pleasanton, CA. This position offers a great challenge al...
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. The Technical Writer will be responsible for the technical, clinical and regulatory writing of laboratory and quality system documentation. This position will be responsible for translating procedures and data into laboratory and regulatory compliant materials. The Technical Writer will communicate with quality specialists, scientists and laboratory personnel. The ideal candidate will be experie...
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Document Preparation / Document Management • Plan, write, edit, review and coordinate the approval of lab operating procedures and scientific validations to support pharma sponsors or internal use. • Facilitate trial development and product registration. • Ensure and coordinate quality checks for accuracy, collates reviewer’s comments, adjusts content of document as required based on internal/exte...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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Frontage Labs, a fast growing CRO located in Exton, PA is seeking a TECHNICAL WRITE/QC COORDINATOR. General Description: ) Review the scientist's lab notebook and data package; 2) Write method validation, sample analysis reports, study protocols/plans and bioanalytical methods; 3) Manage bioanalytical documentation; 4) Oversee the proper use and completion of the documentation change control forms...
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GENERAL SUMMARY: Develops, writes, and finalizes the strategic documents that accompany PRA proposals. Ensures the strategic document development processes, as a part of the proposal; process, are followed and that the appropriate strategic discussion occurs during the proposal team strategy meetings. ACCOUNTABILITIES: 1. Interacts with proposal development team to ensure essential strategic infor...
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Posting date: April 19, 2013 Company Information About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of $12 billion, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and cli...
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Job ID: 447 Position Description: This position works within the Editorial Services group to review planned promotional materials and programming initiatives, both print and electronic, for Forest brands. Position provides editorial support at all stages of the promotional review process and is responsible for research and reference checks regarding data and claims, grammatical and factual accurac...
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Johnson & Johnson companies are equal opportunity employers. WW Manager of Document Management-9825121126 Description DePuy Synthes Companies of Johnson & Johnson is recruiting for a WW Manager of Document Management, this position may be located in any of the major DePuy Synthes companies; Raynham, MA, West Chester, PA, Warsaw, IN, Cork, Ireland or Switzerland. DePuy Synthes Companies of Johnson ...
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About Epocrates, Inc. Epocrates, Inc., an athenahealth company, is recognized for developing the #1 medical application among U.S. physicians for clinical content, practice tools, and health industry engagement at the point of care. Epocrates has established a loyal network of more than one million health care professionals, including 50 percent of U.S. physicians, who routinely use its intuitive ...
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1.The goal for this position is to apply proofreading skills to reinforce understanding and execution of the WW Graphics & Labelling strategy and support Product Labelling development efforts. • Key to the proofreader’s success will be the ability to work collaboratively yet independently, focus on details, support day-to-day deadlines, incorporate strategic messaging in their design process • The...
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Johnson & Johnson companies are equal opportunity employers. Group Leader, Sterilization Chemistry-2228130319 Description Advanced Sterilization Products (ASP), a Division of Johnson & Johnson&'s Global Medical Solutions Group is recruiting for a Group Leader, Sterilization Chemistry, located in Irvine, CA. ASP (Advanced Sterilization Products), a member of the Johnson & Johnson Family of Companie...
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Company Description: Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health. The pharmaceutical industry is a complex...
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SUMMARY Stila Cosmetics has an excellent opportunity for a highly motivated Copywriter to contribute to our in-house online and marketing team. We are looking for an enthusiastic, organized person to help capture the season's important fashion/cultural trends and keep our online advertising modern, innovative, and inspired. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties ...
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QD Healthcare Group, a dynamic and growing medical communications company in Stamford, CT, seeks an Editorial Assistant to work on-site in a challenging and stimulating environment. We welcome dedicated and motivated individuals seeking career growth opportunities. Responsibilities Process reference and permission requests (reconcile resulting invoices) Style reference annotations and prepare docu...
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