FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in technical and medical writing, with a strong focus on regulatory compliance and informed consent documentation. Proficient in editing and collaborating on research documents while maintaining high attention to detail and adherence to guidelines.
Highest-signal resume keywords
Technical/Medical WritingRegulatory ComplianceEditing Consent FormsHuman Subjects Research TrainingInterpersonal Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Technical WritingEditingRegulatory ComplianceMedical TerminologyDocument ReviewAttention to DetailProblem-SolvingProject ManagementInformed ConsentResearch Documentation
Soft Skills
Communication SkillsCustomer ServiceCollaborationIndependenceProfessionalism
Tools & Technologies
Word ProcessingExcelPowerPointSlackZoomRingCentralWeb-Based Software
Certifications & Qualifications
Human Subjects Research TrainingCITI Training
Industry Keywords
FDAHHSHealth CanadaICH GCPTCPS2Advarra ProceduresHuman Subject ProtectionsDrug ResearchDevice ResearchCosmetic Research
About the role
Key responsibilities & impact- Conduct accurate pre-reviews of new and revised consent forms for regulatory compliance with FDA, HHS, Health Canada, TCPS2, ICH GCP, and Advarra procedures
- Edit new and revised consent forms to meet regulatory standards and Advarra document requirements
- Incorporate negotiated Sponsor language according to client agreements
- Collaborate with Board members and staff to incorporate stakeholder edits
- Maintain and enhance knowledge of U.S. and/or Canadian regulations and guidelines concerning human subject protections, drug, device, and cosmetic research
- Complete recurring human subjects research training
- Attend at least one IRB meeting monthly, or two monthly during initial training
- Suggest process improvements to management
- Perform other assigned duties
Requirements
What you’ll need- 1+ years of experience in technical/medical writing and/or editing
- Bachelor’s degree
- Experience writing and/or editing consent forms or other research documents
- Proficiency in word processing and editing, including Tracked Changes and Compare Merge functions
- Familiarity with Excel, PowerPoint, Slack or similar direct messaging applications, Zoom or RingCentral or similar remote meeting applications, and web-based proprietary software
- Ability to communicate clearly and professionally in English, verbally and in writing
- Strong interpersonal skills and customer service ability
- Knowledge of human subjects research and informed consent
- Familiarity with scientific/medical terminology and ability 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 multiple editing projects under conflicting demands and priorities
- High attention to detail, accuracy, thoroughness, and problem-solving skills
- Ability to follow written and verbal instructions and work independently
- Must complete recurring Human Subjects Research Training, such as CITI
- Must fulfill organizational training requirements
- Ability to sit or stand for extended periods at a stationary workstation
- Ability to regularly carry, raise, and lower objects up to 10 lbs.
Benefits
Comp & perks- Variable bonus eligibility
- Health coverage
- Paid holidays