... science could directly shape how AI understands and reasons about medical evidence? We're looking ... Clear and precise written communicator - able to document findings and feedback with authority * No ...
... science could directly shape how AI understands and reasons about medical evidence? We're looking ... Clear and precise written communicator - able to document findings and feedback with authority * No ...
Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and ... Able to communicate complex clinical findings clearly and concisely in written form * No prior AI ...
Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and ... Able to communicate complex clinical findings clearly and concisely in written form * No prior AI ...
Freelance Science Writing information
See Indiana salary details
$7.09 - $9.30
5% of jobs
$9.30 - $11.50
0% of jobs
$11.50 - $13.70
1% of jobs
$13.70 - $15.91
2% of jobs
$15.91 - $18.11
3% of jobs
$19.36 is the 25th percentile. Wages below this are outliers.
$18.11 - $20.32
23% of jobs
The median wage is $21.42 / hr.
$20.32 - $22.52
30% of jobs
$24.02 is the 75th percentile. Wages above this are outliers.
$22.52 - $24.72
15% of jobs
$24.72 - $26.93
6% of jobs
$26.93 - $29.13
6% of jobs
$29.13 - $31.34
7% of jobs
$7
$22
$31
How much do freelance science writing jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Freelance Science Writer, and why are they important?
How do freelance science writers typically find and secure consistent work?
What is freelance science writing?
What is the difference between Freelance Science Writing vs Scientific Content Writer?
| Aspect | Freelance Science Writing | Scientific Content Writer |
|---|---|---|
| Credentials | Typically requires a degree in science or related field, writing experience | Often requires a degree in science, communication, or journalism |
| Work Environment | Independent, remote, project-based | Usually employed by companies, agencies, or media outlets |
| Employer & Industry | Clients across various industries, including publishing, education, biotech | Organizations producing scientific articles, reports, or educational content |
Freelance Science Writers work independently on diverse projects for multiple clients, often remotely. Scientific Content Writers are typically employed by organizations to produce consistent scientific materials. Both roles require scientific knowledge and strong writing skills, but Freelance Science Writers enjoy more flexibility and varied assignments, while Scientific Content Writers often have a more structured work environment.
Full-time
Posted 9 days ago
Job description
About the Role
What if your career-long expertise in clinical trial design and regulatory science could directly shape how AI understands and reasons about medical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to frontier AI research - ensuring the clinical data and analyses powering next-generation AI systems meet the same exacting standards expected in real-world regulatory submissions.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to contribute to something genuinely new. No AI background required - just deep command of clinical research and a sharp eye for scientific quality.
- Organization
: Alignerr - Type
: Hourly Contract - Location
: Remote - Commitment
: 10-40 hours/week What You'll Do - Design and critically review clinical trial protocols used to generate high-quality, regulatory-grade datasets for AI training
- Interpret and audit clinical trial results for accuracy, consistency, and alignment with regulatory expectations
- Evaluate AI-generated clinical analyses for scientific soundness and methodological integrity
- Provide structured expert feedback that directly improves how AI models reason about clinical evidence, outcomes, and trial data
- Work independently and asynchronously - fully on your own schedule
- Senior-level experience designing clinical trial protocols intended for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent global bodies
- Strong grounding in clinical research methodology, biostatistics, or translational science
- Naturally detail-oriented with a rigorous, systematic approach to evaluating scientific quality
- Clear and precise written communicator - able to document findings and feedback with authority
- No prior AI or tech experience required
- Prior involvement in data annotation, data quality assurance, or evaluation systems
- Experience reviewing or contributing to clinical evidence packages for drug, device, or diagnostic submissions
- Background spanning multiple therapeutic areas or trial phases
- Familiarity with AI-generated content or model evaluation workflows
- Work directly on frontier AI systems with real impact on clinical and biomedical research
- Fully remote and flexible - work when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level work
- Influence how AI understands, evaluates, and communicates real-world clinical evidence
- Potential for ongoing work and contract extension as new projects launch