Associate/Principal Medical Writer

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    "jobOpeningName": "Associate/Principal Medical Writer",
    "departmentLabel": "Medical Writing",
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    "datePosted": "2025-12-08",
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      "city": "Cambridge",
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    "description": "<p><span><span>Senior/Principal Medical Writer – Remote/Hybrid/In Office - UK</span></span></p>\n<p><span><span>Trilogy Writing &amp; Consulting</span><span>, An </span><span>Indegene</span><span> Company,</span><span> is currently looking to hire Senior</span><span>/Principal</span><span> Medical Writers (</span><span>f</span><span>/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry. At Trilogy, you will be part of a team that provides a service that goes beyond just writing. Our writers are integral parts of clinical development teams supporting the writing and coordinati</span><span>on</span><span> of successful documentation across a broad spectrum of therapeutic areas. </span><span>As a growing company, there</span><span> is room to develop with us… and your ideas will form our future together. </span></span></p>\n<p><span><br></span></p>\n<p><span><span>Applicants must live in one of the following countries: The UK, Germany, Italy, </span><span>I</span><span>reland</span><span>, or Portugal</span><span>. </span></span><span> </span></p>\n<p><span><span>As a Senior</span><span>/Principal</span><span> Medical Writer</span><span> you will:</span></span><span> </span></p>\n<ul>\n<li><span><span>Prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) as the lead writer in collaboration with members of client authoring teams and supported by other writers, as </span><span>appropriate</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Ensure that all documents are produced according to agreed timelines, </span><span>monitor</span><span> and manage project budgets, adhere to relevant SOPs, and meet the requirements of Trilogy as well as the company’s clients.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Be responsible for</span><span> </span><span>providing</span><span> document-specific advice to clients.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Oversee and coordinate other writers and QC specialists </span><span>assisting</span><span> on documents under your responsibility.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Project manage the timelines and review cycles of your documents.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Work in the client’s regulatory document management systems.</span></span><span> </span></li>\n</ul>\n<p><span><span>The candidate must have the following writing experience:</span></span><span> </span></p>\n<ul>\n<li><span><span>Several years of professional experience actively writing regulatory documents.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Worked as the lead writer on &gt;3 (Senior Medical Writer) or &gt;5 (Principal Medical Writer) of at least 3 of the following: Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>For the Principal Medical Writer level, experience in at least 2 </span><span>different types</span><span> of CTD dossiers (</span><span>i.e.</span><span> full new chemical entity application, a variation, a generic dossier, an </span><span>orphan drug dossier, a literature-based dossier [</span><span>e.g.</span><span> a full-mixed application under Article 8(3) of Directive 2001/83/EC]).</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Experience interacting directly with clients or authors of </span><span>the documents</span><span> and coordinating review cycles, meetings, and project timelines.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>For the Principal Medical Writer level, </span><span>ability</span><span> and willingness to take on any project for which a Lead Writer is needed.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Competency in the use of document management systems and review tools.</span></span><span> </span></li>\n</ul>\n<p><span> </span></p>\n<p><span><span>In addition to having the above writing experience, applicants must have:</span></span><span> </span></p>\n<ul>\n<li><span><span>Diploma/Masters/</span><span>Bachelor’s degree in science</span><span>/pharmacy (Ph.D. not necessary).</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Fluent written and spoken English skills.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>An appreciation for a well-written document and an eye for details.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Excellent, proven interpersonal skills and enjoy proactively </span><span>participating</span><span> on a team with diverse personalities.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Flexibility and the ability to stay focused under tight timelines.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Must live in the UK, Germany, Italy, Ireland, or Portugal.</span></span><span> </span></li>\n</ul>\n<p><span><span>Remuneration will be </span><span>relative</span><span> to the level of experience, with all standard Trilogy benefits.</span></span><span> </span></p>\n<p><span><span>Only candidates who meet the following requirements will be considered:</span></span><span> </span></p>\n<ul>\n<li><span><span>Applicants will work fully remote</span><span>ly,</span><span> or</span><span> hybrid remotely</span><span> </span><span>from </span><span>o</span><span>u</span><span>r UK office in Cambridge</span><span>. Freelancers need not apply.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Submission of documents in English.</span></span></li>\n</ul>\n<ul>\n<li><span><span>Cover letter specifying how you </span><span>comply with</span><span> the experience requirements listed above.</span></span></li>\n</ul>\n<ul>\n<li><span><span>CV</span></span><span> </span></li>\n</ul>\n<p><span> </span></p>\n<p><span><span>Trilogy Writing &amp; Consulting</span><span>, An </span><span>Indegene</span><span> Company,</span><span> </span><span>complies with</span><span> all laws respecting equal employment opportunity and does not discriminate against applicants </span><span>with regard to</span><span> any protected characteristic as defined by federal, state/provincial, and local law. We </span><span>passionately believe in creating a supportive environment in which everyone can grow, flourish, and do their best work.</span></span><span><br></span><span> </span></p>\n<p><span><span>Collection and use of personal data in the application process: It is important to Trilogy to ensure the highest possible degree of protection for your personal data. All personal data collected and processed within the scope of an application for employment with Trilogy </span><span>are</span><span> protected against unauthorized access and manipulation by technical and organizational </span><span>measures, and</span><span> are not </span><span>forwarded</span><span> to third parties.</span></span><span> <br></span><span><span>Your data will be collected for the purpose of filling employment opportunities offered by Trilogy Writing &amp; Consulting GmbH in Germany or its subsidiaries Trilogy Writing &amp; Consulting Ltd in the UK, and Trilogy Writing &amp; Consulting, Inc. in the USA. By </span><span>submitting</span><span> your data with this </span><span>application</span><span> you consent to its use for this purpose within Trilogy. You can revoke this consent at any time without needing to give a reason by informing us of your revocation under [email protected]. </span><span>In the event of</span><span> revocation, we will </span><span>delete</span><span> your personal data </span><span>immediately</span><span>.</span></span><span> </span></p>",
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