{"id":1674256,"url":"https://alion.io/job/advarra-sr-editor-consent-form-development","title":"Sr Editor, Consent Form Development","company":{"id":2414960,"name":"Advarra","domain":"advarra.com","url":"https://alion.io/company/advarra","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"UltiPro","truth_index":null},"role":"Communications","role_family":"Communications","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":66767,"max":116089,"currency":"USD","period":"year","gross":null,"usd_annual":116089},"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Slack","optional":false}],"status":"closed","first_seen_at":"2026-09-04T15:51:02Z","employer_posted_date":"2026-09-04","last_verified_at":"2026-10-02T22:33:42Z","board_verified":false,"closed_at":"2026-10-02T22:33:42Z","days_open":28,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":28},"description":"Company Information\nAt Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.\nCompany Culture\nOur employees are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.\nAt Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact.\nJob Overview Summary\nSr Editor, Consent Form Development supports the IRB Services department in the review of incoming submissions and preparation of informed consent forms (ICFs) used in the conduct of human subjects research. In addition, the Senior Editor may mentor new editors and complete projects as defined by management.\nJob Duties & Responsibilities\nConduct an accurate pre-review of new and revised consent forms in regulatory compliance with applicable FDA, HHS, Health Canada, TCPS2 regulations, ICH GCP guidance, and operational compliance with Advarra Standard Operating Procedures and Work Instructions \nEdit new and revised consent forms to ensure regulatory compliance and alignment with Advarra operational standards\nApply negotiated Sponsor and site language to consent form documents as required by client agreements documented in mandatory language documents or MLD’s\nCollaborate with Board members and staff to include all necessary edits to the consent form from the various stakeholders\nComplete informed consent quality control check for yourself and others\nMentor new team members, as requested\nMaintain and increase individual regulatory knowledge to assist with organizational compliance:\nMaintain and increase knowledge of U.S. and/or Canadian Regulations and Guidelines in the area of Human Subject Protections, drug research, device research, and cosmetic research\nComplete standard Human Subjects Research Training, such as CITI, on a repeating cycle determined by management\nComplete organizational training as required by management\nAttend one IRB meeting per month to enhance knowledge and understanding of IRB processes (two meetings per month during the initial training period)\nOffer process improvement suggestions to management, as applicable\nOther duties as assigned\nLocation\nThis role is open to candidates working remotely in the United States.\nBasic Qualifications\n2+ years of experience in technical/medical writing and/or editing in addition to a Bachelor’s degree\nExperience writing and/or editing consent forms or other research documents\nProficiency in Word processing and editing (including use of Tracked Changes and Compare Merge functions)\nFamiliar with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom or RingCentral, and web-based proprietary software\nPreferred Qualifications\n1+ years of IRB experience \nExperience writing and/or editing consent forms or other research documents\nCertified IRB Professional (CIP) or completion of CIP within two (2) years of eligibility\nAbility to communicate clearly and professional in English, both verbal and written skills \nExcellent interpersonal skills to work professionally and effectively with others and provide high levels of customer service\nIn-depth knowledge of matters regarding human subjects research and informed consent\nFamiliar with scientific/medical terminology and able to convert scientific/medical information to lay terms\nAbility to edit technical and/or medical documents\nAbility to read and comprehend advanced technical/medical documents such as medical protocols and informed consent forms\nAbility to manage various editing projects under conflicting demands and priorities\nDependably produces high quality work \nMust have high level of attention to detail, accuracy and thoroughness; problem solving skills\nAbility to follow written and verbal instructions and work independently as required\nPhysical and Mental Requirements\nSit or stand for extended periods of time at stationary workstation\nRegularly carry, raise, and lower objects of up to 10 Lbs. \nLearn and comprehend basic instructions\nFocus and attention to tasks and responsibilities\nVerbal communication; listening and understanding, responding, and speaking \nAdvarra is an equal opportunity employer that is committed to providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identity), national origin, age, disability or genetic information, or any other status or characteristic protected by federal, state, or local law.\nPay Transparency Statement\nThe base salary range for this role is $66,767 - $116,089. Note that salary may vary based on location, skills, and experience and may vary from the amounts listed above. This position may also be eligible for a variable bonus in addition to base salary as well as health coverage, paid holidays, and other benefits.","description_format":"text","description_chars":5901,"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":true}]},"benefits":[],"hiring_locations":[{"name":"United States","iso":"US","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Health Care","Clinical Trial Services (CRO)","Clinical Trial Sites & Recruitment"],"lifecycle":[{"event":"open","at":"2026-10-02T07:45:19Z"},{"event":"close","at":"2026-10-02T22:33:42Z"}],"visa":[],"liveness":null,"pay":{"stated_usd_annual":116089,"is_top_pay":false},"html_url":"https://alion.io/job/advarra-sr-editor-consent-form-development","json_url":"https://alion.io/job/advarra-sr-editor-consent-form-development.json","meta":{"generated_at":"2026-10-08T00:24:11Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler","counted_by":"address","units_charged":1,"used_today":489,"day_limit":5000,"remaining_today":4511,"minute_limit":60,"resets_at":"2026-10-09T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":2414960},"rest":"https://alion.io/mcp/rest/get_company?id=2414960"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fadvarra-sr-editor-consent-form-development"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fadvarra-sr-editor-consent-form-development"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fadvarra-sr-editor-consent-form-development"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/advarra-sr-editor-consent-form-development\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fadvarra-sr-editor-consent-form-development"}]}