Advarra

Sr Editor, Consent Form Development

Advarra$66K — $116K *
US-AnywhereRemote in United States
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree plus 2+ years in technical/medical writing/editing
  • Experience with consent forms or research documents
  • Proficiency in Word processing, including advanced editing functions
  • Familiarity with Excel, PowerPoint, and communication tools (Slack, Zoom)
  • 1+ years of IRB experience preferred
  • CIP certification or commitment to obtain within 2 years
  • Strong communication skills in English, both written and verbal

Responsibilities

  • Conduct pre-reviews of consent forms for regulatory compliance
  • Edit consent forms to align with operational standards
  • Incorporate sponsor and site language into documents
  • Collaborate with team and Board members for comprehensive edits
  • Perform quality control checks on informed consent documents
  • Mentor new team members when required
  • Suggest improvements to processes as applicable
  • Attend IRB meetings to enhance knowledge of processes

Benefits

  • Remote work flexibility
  • Health coverage
  • Paid holidays
  • Opportunity for process improvement contributions
  • Active mentorship participation
Full Job Description
Job Overview Summary

Sr 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.

Job Duties & Responsibilities

  • Conduct 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

  • Edit new and revised consent forms to ensure regulatory compliance and alignment with Advarra operational standards

  • Apply negotiated Sponsor and site language to consent form documents as required by client agreements documented in mandatory language documents or MLD's

  • Collaborate with Board members and staff to include all necessary edits to the consent form from the various stakeholders

  • Complete informed consent quality control check for yourself and others

  • Mentor new team members, as requested

  • Maintain and increase individual regulatory knowledge to assist with organizational compliance:

  • Maintain 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

  • Complete standard Human Subjects Research Training, such as CITI, on a repeating cycle determined by management

  • Complete organizational training as required by management

  • Attend one IRB meeting per month to enhance knowledge and understanding of IRB processes (two meetings per month during the initial training period)

  • Offer process improvement suggestions to management, as applicable

  • Other duties as assigned


Location

This role is open to candidates working remotely in the United States.

Basic Qualifications

  • 2+ years of experience in technical/medical writing and/or editing in addition to a Bachelor's degree

  • Experience writing and/or editing consent forms or other research documents

  • Proficiency in Word processing and editing (including use of Tracked Changes and Compare Merge functions)

  • Familiar with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom or RingCentral, and web-based proprietary software


Preferred Qualifications

  • 1+ years of IRB experience

  • Experience writing and/or editing consent forms or other research documents

  • Certified IRB Professional (CIP) or completion of CIP within two (2) years of eligibility

  • Ability to communicate clearly and professional in English, both verbal and written skills

  • Excellent interpersonal skills to work professionally and effectively with others and provide high levels of customer service

  • In-depth knowledge of matters regarding human subjects research and informed consent

  • Familiar with scientific/medical terminology and able to convert scientific/medical information to lay terms

  • Ability to edit technical and/or medical documents

  • Ability to read and comprehend advanced technical/medical documents such as medical protocols and informed consent forms

  • Ability to manage various editing projects under conflicting demands and priorities

  • Dependably produces high quality work

  • Must have high level of attention to detail, accuracy and thoroughness; problem solving skills

  • Ability to follow written and verbal instructions and work independently as required


Physical and Mental Requirements

  • Sit or stand for extended periods of time at stationary workstation

  • Regularly carry, raise, and lower objects of up to 10 Lbs.

  • Learn and comprehend basic instructions

  • Focus and attention to tasks and responsibilities

  • Verbal communication; listening and understanding, responding, and speaking


Pay Transparency Statement

The 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.

About Advarra

Advarra is a leading provider of institutional review board (IRB), institutional biosafety committee (IBC), and research quality and compliance consulting services to the healthcare industry. The company helps healthcare organizations and research institutions navigate the complex regulatory landscape of clinical research, ensuring that their studies are conducted ethically and in compliance with all applicable laws and regulations. Advarra was founded in 2017 and is headquartered in Columbia, Maryland. The company has over 1,000 employees and serves clients across the United States and internationally. Advarra is committed to advancing the field of clinical research and improving patient outcomes through its innovative solutions and services.
Learn more about Advarra
Size
1,000 employees
Industry
Founded
2017

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