Clinical Science Consultant
Remote regions
USBenefits
12w maternity
12w paternity
Similar Jobs
See allClinical Pharmacology Domain Expert
Edison Scientific
Regulatory Submissions
CMC Regulatory Affairs Consultant
Edison Scientific
US
Regulatory Affairs
Pharmaceutical Industry
ICH Guidelines
Biostatistician Consultant
Edison Scientific
US
Biostatistics
Clinical Trial Design
Data Quality
Clinical Research Associate - FSP - Remote
ICON
ICH-GCP
Regulatory Compliance
Communication
Clinical Trials Regulatory Specialist III
Emory University
US
Regulatory Affairs
Clinical Research
Project Management
Responsibilities:
- Serve as subject matter expert defining gold standard for AI-generated clinical content and outputs.
- Share knowledge about day-in-the-life working with data to assemble regulatory submissions.
- Identify and correct discrepancies in data quality.
Qualifications:
- 10+ years of experience in clinical science or clinical development within pharma/biotech.
- Bachelor's degree in life sciences required; advanced degree (MD, PhD, or PharmD) preferred.
- Hands-on experience designing and executing early-phase clinical trials, including protocol development and endpoint selection.
Why Join Us:
- Remote, US-based with flexible hours of 5-20 hours per week.
- No benefits for consulting roles, but full-time positions include competitive salary, equity, 100% healthcare coverage, and 12 weeks paid parental leave.
- Fast-moving, mission-driven culture with regular team offsites and company events.
Edison Scientific
Edison Scientific builds and commercializes AI agents for science to accelerate scientific discovery. They are assembling a small team of top researchers and engineers across AI and biology to build an AI scientist.