Pipeline
Browse Jobs
Sign inSign up
Pipeline
Browse jobsSign inContactTermsPrivacyCookiesPreferences
Logos provided by Logo.dev

© 2026 Pipeline. All rights reserved.

  1. Home
  2. Jobs
  3. Clinical Solutions
  4. Senior Medical Writer
Precision Medicine Group logo

Precision Medicine Group

Senior Medical Writer at Precision Medicine Group

Remote, United StatesFull-timeRemoteClinical SolutionsPosted 22 days ago
Apply with Pipeline→

About the Role

<p><strong><span data-contrast="auto"><span data-ccp-parastyle="Body Text">Position Summary:</span></span><span data-ccp-props="{&quot;134245417&quot;:false,&quot;201341983&quot;:0,&quot;335559685&quot;:504,&quot;335559739&quot;:0,&quot;335559740&quot;:240,&quot;335559991&quot;:504}">&nbsp;</span></strong></p> <p><span data-contrast="none">The&nbsp;Senior&nbsp;Medical Writer&nbsp;(MW)&nbsp;will&nbsp;be responsible for&nbsp;leading the&nbsp;development&nbsp;of high-quality and on-time clinical study documents.&nbsp;Specific responsibilities&nbsp;include&nbsp;clinical document&nbsp;planning, writing, editing/formatting, and performing QC review.&nbsp;Develops&nbsp;documents in&nbsp;compliance&nbsp;with&nbsp;Precision MW Style Guide, Precision&nbsp;SOPs,&nbsp;applicable&nbsp;regulatory guidelines&nbsp;(ie, ICH, FDA, GCP)&nbsp;and eCTD requirements.&nbsp;The successful candidate&nbsp;has a clear understanding of content requirements for key clinical documents based on regulatory requirements for all phases of development and&nbsp;will complete MW activities&nbsp;with&nbsp;impeccable&nbsp;attention to detail.</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></p> <p><span style="text-decoration: underline;"><span data-contrast="none">Essential functions of the job include but are not limited to:</span><em><span data-contrast="none">&nbsp;</span></em> </span></p> <ul> <li><span data-contrast="none">Planning, writing, editing, formatting, and QC review of timely and high-quality clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear understanding of content requirements based on regulatory guidances&nbsp;</span></li> <li><span data-contrast="none">Ensures smooth and effective document management from start to finish (ie, from template to final, approved version) in collaboration with Sponsor, external vendors, and/or internal Precision project teams/departments</span></li> <li>Ability to independently formulate key messages from clinical study data&nbsp;</li> <li>Ability to author complex content using knowledge/skills and understanding of processes</li> <li>Ability to communicate clearly and concisely both in writing and verbally with internal and client teams</li> <li>Contributes to the development and maintenance of medical writing processes, SOPs, templates, and work instructions for key documents</li> <li>Excellent problem-solving skills</li> <li>Performing literature-based research to support writing activities</li> <li>Other duties as assigned<span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></li> </ul> <p><strong><span data-contrast="none">Qualifications:</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></strong></p> <p><span style="text-decoration: underline;"><span data-contrast="none">Minimum Required:</span></span></p> <ul> <li><span data-contrast="none">BS degree or equivalent in a scientific or medical discipline with relevant writing expertise</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></li> <li data-leveltext="" data-font="Symbol" data-listid="8" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}" data-aria-posinset="11" data-aria-level="1"><span data-contrast="none">5+&nbsp;years of experience as a medical writer in the sponsor and/or CRO setting</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></li> </ul> <p><span style="text-decoration: underline;"><span data-contrast="none">Other Required:</span> </span></p> <ul> <li><span data-contrast="none">Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></li> <li><span data-contrast="none">Clear understanding of applicable regulations (eg, ICH, FDA, GCP), clinical trial transparency requirements (ie, EudraCT, CT.gov), and eCTD requirements for all phases of development</span></li> <li>Impeccable attention to detail and ability to complete writing assignments in a timely manner&nbsp;</li> <li>Ability to work effectively in a fast-paced environment with multiple high priority projects with no instruction on routine work and minimal instruction on new assignments<span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></li> </ul> <p><span style="text-decoration: underline;"><span data-contrast="none">Preferred:</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></span></p> <ul> <li data-leveltext="" data-font="Symbol" data-listid="8" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}" data-aria-posinset="16" data-aria-level="1"><span data-contrast="none">Advanced degree (MS/PhD)</span></li> <li data-leveltext="" data-font="Symbol" data-listid="8" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}" data-aria-posinset="16" data-aria-level="1">Oncology and/or rare disease experience (especially protocol and CSR development)<span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:60,&quot;335559740&quot;:240}">&nbsp;</span></li> </ul> <p>&nbsp;</p><div class="content-pay-transparency"><div class="pay-input"><div class="description">Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case.&nbsp; This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.</div><div class="title">Reasonable estimate of the current range</div><div class="pay-range"><span>$100,600</span><span class="divider">&mdash;</span><span>$151,000 USD</span></div></div></div><div class="content-conclusion"><p>Any data provided as a part of this application will be stored in accordance with our <a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&amp;data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&amp;reserved=0">Privacy Policy.</a>&nbsp;For CA applicants, please also refer to our&nbsp;<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&amp;data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&amp;reserved=0">CA Privacy Notice</a>.</p> <p>Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.</p> <p>If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at&nbsp;<a href="mailto:[email protected]">[email protected]</a>.</p> <p>It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.</p></div>

Related Roles

  • Senior/Clinical Research Associate

    Precision Medicine Group

    Remote, South KoreaRemote
  • Clinical Trial Manager (Shanghai/Beijing)

    Precision Medicine Group

    Remote, ChinaRemote
  • Regulatory and Site Start Up Specialist

    Precision Medicine Group

    Remote, South KoreaRemote
  • Senior Clinical Data Manager (Mexico)

    Precision Medicine Group

    Remote, MexicoRemote
  • Clinical Data Manager II/Senior Clinical Data Manager

    Precision Medicine Group

    Remote, PolandRemote
  • Clinical Data Manager II/Senior Clinical Data Manager

    Precision Medicine Group

    Remote, SlovakiaRemote