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Hire the best Research Documentation Freelancers in Minneapolis, MN

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Bruce L.

Minneapolis, Minnesota

$25/hr
5.0
1 jobs
I specialize in evaluating and refining AI-generated outputs with precision and care. My focus is on AI annotation, content review, and prompt testing — ensuring accuracy, clarity, and alignment with human expectations. With 30+ years as a licensed architect and sole proprietor, I bring a proven record of delivering detail-oriented, client-focused results. That experience sharpened my ability to detect discrepancies, manage complex projects, and communicate clearly — strengths I now apply directly to AI training and evaluation. Key strengths include: -AI data annotation & evaluation -Prompt testing & content review -Language analysis & detail verification -Clear written communication & reporting I work best in focused, independent settings where thoughtful judgment matters most. If you need reliable, meticulous evaluation of AI outputs, I’m ready to contribute immediately.
  • Research Documentation
  • Copy Editing
  • Grammar & Syntax Review
  • Content Analysis
  • AI Content Editing
  • Fact-Checking
  • Accuracy Verification
  • Data Annotation
  • Data Labeling
  • Prompt Engineering
  • Content Moderation
  • Sentiment Analysis
  • Chatbot Prompt
  • Chatbot Script
  • AI Chatbot
Jennifer J.

Minneapolis, Minnesota

$25/hr
1 jobs
Born and raised in Minnesota, I've also had the adventure of living on both the West and East Coasts before finally returning to my roots. Outside of work, I'm all about embracing life's experiences whether that means catching live music events (nothing beats the energy of a great concert), cheering on the Minnesota Timberwolves, or taking a leisurely bike ride in warm weather. I love finding creative outlets and am never afraid to get my hands dirty-both literally and figuratively. And yes, in true midlife crisis fashion, I returned to school and achieved a UX/UI design certificate. It's my way of staying curious and continuously evolving my skill set. I'm excited to blend my passion for customer success with fresh design insights, ensuring that every experience is as innovative as it is customer-focused.
  • Research Documentation
  • Figma
  • Canva
  • SnagIt
  • Web Design
  • Mobile App Design
  • FigJam
  • Slack
  • Zoom Video Conferencing
  • Customer Discovery
  • Customer Engagement
  • Research & Strategy
  • Research Interviews
  • Recruiting
  • Recruiting Process Consulting
Gavin M.

Minneapolis, Minnesota

$70/hr
Experienced Clinical Research Associate (CRA) | Data Management | Regulatory Compliance | Clinical Trial Monitoring Hello! I’m Gavin Mark, a highly skilled Clinical Research Associate (CRA) with a proven track record of overseeing and supporting clinical trials from initiation through to close-out. With extensive experience in clinical research, data management, and regulatory compliance, I help ensure that clinical trials are conducted efficiently, ethically, and in accordance with industry standards. I specialize in: • Clinical Trial Management: Planning, executing, and monitoring clinical trials across various phases, ensuring adherence to Good Clinical Practice (GCP) and regulatory guidelines. • Data Management & Analysis: Handling complex data collection and ensuring accurate reporting for study milestones. • Regulatory Documentation & Compliance: Reviewing and assisting in preparing regulatory submissions, protocol development, and site management to ensure all legal and ethical standards are met. • Site Monitoring & Investigator Communication: Building strong working relationships with clinical sites, investigators, and project teams to ensure smooth trial progress and issue resolution. I have a comprehensive understanding of the clinical research lifecycle and am committed to providing high-quality, reliable, and accurate support to both large pharmaceutical companies and smaller research teams. If you’re looking for a CRA who is highly detail-oriented, organized, and dedicated to the success of your clinical trials, let’s connect! I can offer flexible and dependable solutions to meet your project needs. Additional Skills & Expertise: • Clinical Trial Monitoring & Reporting • Pharmaceutical & Biotechnology Industry Expertise • Protocol Review & Amendment • Regulatory Compliance (FDA, ICH, GCP) • SOP Development & Training • Data Integrity & Statistical Reporting • Study Coordination & Site Support I look forward to collaborating on your next project!
  • Research Documentation
  • Data Entry
  • Clinical Trial
  • Clinical Trial Management System
  • Data Analysis
  • General Transcription
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