{"id":1124830,"url":"https://alion.io/job/trident-consulting-medical-writer","title":"Medical Writer","company":{"id":690486,"name":"Trident Consulting","domain":"tridentconsultinginc.com","url":"https://alion.io/company/tridentconsultinginc","size_band":null,"is_staffing_agency":false,"is_intermediary":false,"ats_vendor":"SmartRecruiters","truth_index":null},"role":"Communications","role_family":"Communications","seniority":"junior","employment_type":"contractor","work_mode":"on_site","remote_scope":null,"hiring_geo_confidence":"structured","locations":["Aliso Viejo, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":42,"max":44,"currency":"USD","period":"hour","gross":null,"usd_annual":88000},"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-09-21T22:58:59Z","employer_posted_date":"2026-09-21","last_verified_at":"2026-09-23T19:24:13Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"About Trident:\nTrident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology\nSome of our recent awards include:\n2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America\n2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area\n Role: Medical Writer II\nLocation: Aliso Viejo, CA (contract-onsite)\nDuration: 6 Months\nPay: $42- $44/hr on W2(Inclusive all)\nShift: 1st Shift\nDescription\nPOSITION OVERVIEW: (An Overview of the Department & Summary of the Role)\nThis role will be responsible for producing high-quality clinical and clinical regulatory documentation that requires a strong understanding of medical and regulatory concepts and terminology, as well as the ability to translate complex information into clear and concise documentation.\nThe Medical Writer II will work closely and collaborate with project teams spanning multiple departments on Client' current and pipeline products.\nThe Medical Writer II will be responsible for determining the clearest and most logical way to present clinical and scientific information.\nThe individual will ensure that documentation is accurate, complete, meets editorial and quality standards, and adheres to established regulatory guidelines, templates, and company procedures.\nResponsibilities:\n(Essential Functions and Associated Tasks for the Role)\nPrepare clinical study reports (CSRs) under supervisor direction. Based on the clinical study protocol and statistical analysis plan, translate clinical results data tables, listings, and figures into a report of study outcomes, complete final checks for data consistency, and ensure compliance with applicable regulatory requirements.\nTranslate clinical study synopses into full clinical study protocols, ensuring appropriate depth, technical accuracy, and consistency. Collaborate with project team members to gather required input and feedback. • Interpret data, analyze results, and apply knowledge of scientific, regulatory, and compliance requirements to document preparation.\nSystematically review reports and clinical data and cross-check information for completeness and accuracy.\nEnsure consistency in style, tone, and quality across all assigned documents.\nConduct medical and scientific literature searches to support clinical and regulatory documentation.\nReview, edit, and cross-check documents produced by team members for clarity, accuracy, consistency, and compliance.\nStay current with industry trends, regulatory requirements, and best practices in medical writing and clinical research.\nDevelop and maintain lists of abstract submission deadlines, and key dates for major ophthalmology and related scientific conferences.\nCoordinate with Clinical, and R&D teams to support conference abstract submissions while ensuring compliance with conference guidelines and company objectives.\nPrepare, edit, and proof presentations, slide decks, posters, and other scientific communications for internal and external stakeholders.\nAssist in the development of figures, tables, and graphical content for publications, presentations, and posters.\nManage multiple writing assignments simultaneously and prioritize deliverables to support project timelines.\nParticipate in project team meetings and provide updates regarding documentation status and deliverables.\nRequirements\nWork experience:\n(Provide Experience, Knowledge, Skills & Abilities Required for the Role)\n2-5 years of relevant experience in clinical research, medical writing, life sciences, biotechnology, pharmaceutical, or medical device industries.\nStrong understanding of clinical research methodologies, medical terminology, and scientific principles. • Working knowledge of regulatory requirements and guidance applicable to clinical and regulatory documentation.\nExperience supporting clinical study reports, protocols, publications, abstracts, posters, or similar scientific documents preferred.\nFamiliarity with publication development and scientific communication processes preferred. • Ophthalmology experience preferred.\nExcellent writing, editing, proofreading, and organizational skills.\nStrong attention to detail and ability to evaluate complex scientific information.\nProficiency with Microsoft Office Suite, Adobe Acrobat, and document management systems.\nStrong project management, communication, and interpersonal skills.\nAbility to work independently while collaborating effectively within cross-functional teams.\nEducation:\nBachelor's degree in Life Sciences, Biology, Chemistry, Biomedical Engineering, Pharmacy, Public Health, or a related scientific discipline required. Advanced degree (MS, PharmD, OD, PhD, MPH, or equivalent) preferred.\nAll your information will be kept confidential according to EEO guidelines.","description_format":"text","description_chars":4858,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[{"language":"English","level":"All levels","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology"],"lifecycle":[{"event":"open","at":"2026-09-22T20:53:26Z"}],"liveness":{"score":78,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.781,"p_room":1,"age_days":2,"expected_fill_days":10,"reasons":["conf:10","win:early","comp:junior"],"computed_at":"2026-09-24T05:45:00Z"},"pay":{"stated_usd_annual":88000,"is_top_pay":true},"html_url":"https://alion.io/job/trident-consulting-medical-writer","json_url":"https://alion.io/job/trident-consulting-medical-writer.json","meta":{"generated_at":"2026-09-24T08:47:04Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers"}}