Mercor
This role involves reviewing clinical reports, technical reviews, and grant proposals for clarity and rigor, evaluating experimental methodologies, and drafting concise technical summaries of research methods and results. The specialist will also provide structured responses to analytical prompts and collaborate asynchronously with project coordinators to ensure consistency and quality.
Key Responsibilities
- • Review clinical reports, technical reviews, and grant proposals for clarity and rigor.
- • Evaluate experimental methodologies and interpret their validity in supporting outcome claims.
- • Draft concise, technical summaries of research methods and results.
- • Provide structured responses to specific analytical prompts.
- • Collaborate asynchronously with project coordinators to ensure consistency and quality.
Required
- • 3+ years of experience in academic publishing, research analysis, or clinical data interpretation.
- • Advanced degree in a relevant field (e.g., MPH, PhD, PharmD, MD).
- • Proven ability to synthesize and assess complex research data.
- • Strong technical writing and analytical reasoning skills.
Company Overview
Industry: Healthcare Technology
Company Size: 500-1,000 employees
Founded: 2015
Headquarters: San Francisco, CA
Company Links
Key Contacts
Contact information not available
About the Company
Leading healthcare technology company focused on improving patient outcomes through innovative digital solutions. We're transforming the way healthcare is delivered with cutting-edge technology and data-driven insights. Our platform serves over 10,000 healthcare professionals and has processed millions of patient interactions.
Recent News & Updates
Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.
Position: Technical Documentation Specialist
Type: Part-time Contract
Compensation: $50–$70/hour
Location: Remote
Commitment: 10–20 hours/week
Role Responsibilities
- Review clinical reports, technical reviews, and grant proposals for clarity and rigor.
- Evaluate experimental methodologies and interpret their validity in supporting outcome claims.
- Draft concise, technical summaries of research methods and results.
- Provide structured responses to specific analytical prompts.
- Collaborate asynchronously with project coordinators to ensure consistency and quality.
Must-Have
- 3+ years of experience in academic publishing, research analysis, or clinical data interpretation.
- Advanced degree in a relevant field (e.g., MPH, PhD, PharmD, MD).
- Proven ability to synthesize and assess complex research data.
- Strong technical writing and analytical reasoning skills.
- $60/hour for U.S.-based professionals.
- Paid weekly via Stripe Connect.
- Classified as an independent contractor.
- Submit a brief resume or portfolio highlighting relevant experience.
- Selected applicants may be asked to complete a short sample prompt.
- For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome/welcome
- For any help or support, reach out to: [email protected]
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