Similar Jobs
See allClinical Science Consultant
Edison Scientific
US
Clinical Development
Regulatory Submissions
ICH Guidelines
Clinical Pharmacology Domain Expert
Edison Scientific
Regulatory Submissions
CMC Regulatory Affairs Consultant
Edison Scientific
US
Regulatory Affairs
Pharmaceutical Industry
Biotechnology
Medical Director
HealthMatch
US
Process Optimization
Cross-functional Collaboration
Principal Medical Writing Domain Expert
Veeva Systems
US
Medical Writing
Regulatory Guidelines
Communication
The Role:
- Engage with domain experts to design and build AI tasks for regulatory submissions.
- Describe common tasks where AI could add value in your workflows.
- Identify and correct discrepancies in data quality.
Qualifications:
- 15+ years in pharmaceutical/biotechnology industry with MD required.
- Experience in Oncology therapeutic area preferred.
- Strong knowledge of clinical trial methodology across Phase I-IV.
Why Join:
- Remote, US-based with flexible hours (5-20 hours per week).
- Mission-driven culture where smart people do their best work.
- Note: This consulting role does not offer benefits.
Edison Scientific
Edison Scientific builds and deploys AI scientist agents to accelerate science and the development of new medicines. The team is ambitious and run by scientists and engineers from leading institutions across biology, physics, chemistry, and AI.