Science Writer Salary in District of Columbia

Principal Medical Writer Job Description: Meet's partnered with a top 10 pharma who is looking for an enthusiastic and passionate Principal Medical Writer to join their immunology team! This role will be responsible for individually contributing to and leading the writing of clinical stage/study level documents. This is an incredible remote opportunity for someone who values great leadership, supportive culture and an exciting workload! Job Responsibilities: Contribute to the preparation and submission of regulatory and clinical stage documents (CSRs, IBs, protocols, INDs and submission work) Provide expert support to clinical teams and liaise with internal and external departments effectively Serve as lead author and help manage timelines Skills Required: Advanced science degree preferred; Bachelor’s degree required 5+ years of experience in regulatory writing; prior experience in a pharmaceutical environment preferred Knowledge of FDA/international regulations and ICH guidelines Exce

Science Writer - Non-teaching Adjunct, Level 3 New York , New York Science Writer - Non-teaching Adjunct, Level 3 Job ID 23670 Location Graduate Center Full/Part Time Regular/Temporary Regular **GENERAL DUTIES** Completes non-teaching projects or complex work in support of a Campus or University administrative or academic department. This work is generally of a temporary nature and requires specialized experience or expertise. **CONTRACT TITLE** Non-Teaching Adjunct **FLSA** Exempt **CAMPUS SPECIFIC INFORMATION** The Graduate Center of The City University of New York (CUNY) is seeking an excellent science journalist to cover discoveries in the sciences and social sciences made by faculty, student, and alumni researchers who are advancing knowledge of the natural world. The Graduate Center is home to nearly 50 Ph.D. and masters programs, 16 of them in STEM-related fields, and encompasses a state-of-the-art Advanced Science Research Center. The Science Writer will write news stories, pro

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency,and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma’sinternational awards programs for the last three consecutive years. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn. Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical signifi

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma’sinternational awards programs for the last three consecutive years. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn. We are looking for consultants interested in joining our extended team! Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency,and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma’sinternational awards programs for the last three consecutive years. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn. Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical signifi

Purpose of the Position The Science Writer II role is responsible for strengthening Thorlabs' position as a leading manufacturer of Photonics products through the creation of effective technical content that informs and educates the photonics community about Thorlabs' products and their applications. This role will demonstrate a firm understanding of Thorlabs' extensive product portfolio via the delivery of high-quality website content, tradeshow materials, and other marketing collateral. The Science Writer II will be able to draw on their existing technical experience and photonics knowledge to engage in meaningful conversations with engineering teams to support product revisions, product feedback, and general website improvements; propose and plan changes to Thorlabs' website to enhance the buying experience for customers; and successfully execute their plans to produce high-quality content requiring minimal feedback. This role works closely with graphic artists to create presentatio