Biotech Health Data Governance Lead
Role Overview
Biotech Health Data Governance Lead role supporting AI training and evaluation in life sciences research.
Ensure research and clinical trial data is accurate, traceable, compliant, and scientifically trustworthy.
Fully remote, flexible contract role for experienced professionals.
Hourly contract with a stated commitment of 10–40 hours per week.
Key Skills for This Role
Full Job Posting
Role overview
Biotech Health Data Governance Lead role supporting AI training and evaluation in life sciences research.
Ensure research and clinical trial data is accurate, traceable, compliant, and scientifically trustworthy.
Fully remote, flexible contract role for experienced professionals.
Hourly contract with a stated commitment of 10–40 hours per week.
What you'll do
- Govern biotech research and clinical trial datasets for accuracy, lineage, and auditability in scientific analysis and regulatory submissions.
- Define and enforce policies for data classification, access controls, security protocols, and metadata standards.
- Enable secure data access for analytics, AI model development, and external collaboration while protecting confidential and patient-related information.
- Improve data quality workflows, annotation standards, and readiness for AI training pipelines.
- Collaborate across scientific, IT, compliance, business, and partner teams to align governance with operational and regulatory requirements.
- Support scalable, auditable data governance practices for life sciences and AI research.
Who you are
- Experience leading or implementing governance programs in biotech, life sciences, clinical research, or another regulated data environment.
- Deep knowledge of privacy, security, compliance, and regulatory expectations for research and clinical trial data.
- Able to translate governance requirements into actionable standards for scientific, technical, and business teams.
- Detail-oriented and systematic, with clear documentation practices.
- Self-directed and reliable in a remote, asynchronous environment.
Preferred experience
- Data annotation, data quality assurance, or AI data evaluation experience is a plus.
- Familiarity with FDA 21 CFR Part 11, GCP, HIPAA, or ICH guidelines is a plus.
- Clinical data management, bioinformatics, or health informatics background is a plus.
- Experience working with AI or machine learning teams in data governance is a plus.
Workplace and schedule
- Fully remote and flexible work arrangement.
- Hourly contract engagement with a stated commitment of 10–40 hours per week.
Engagement
- Work at the intersection of AI and life sciences on research projects.
- Potential for ongoing work and contract extension as new projects launch.
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