GLP QA Consultant
Listed on 2026-10-30
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IT/Tech
Data Analyst
LOGISTICS:
Level: Director, VP
Hourly Rate: $120 - $245 /hour
Hours per week: 20 hours
Duration: 1 month
Remote - some travel to site required
This is a 1099 Consulting Opportunity
ABOUT:
We are a VC-backed biotech combining proprietary technologies to identify cell-specific receptors and optimized ligands for the development of siRNA therapies for the treatment of musculoskeletal diseases, heart failure, and metabolic disorders.
We are looking for a pharmacology/toxicology consultant or a GLP QA consultant from a pharmacology/toxicology background to conduct an on-site audit of an executed PK/TK/PD study, review reported data against source data for integrity, and ensure compliance of data and source systems used to generate data.
Responsibilities:
- Independently conduct an on-site (at least one week) audit of an executed tox/pharm study.
- Review reported data against source data for integrity
- Ensure compliance of data and source systems used to generate data
Ideal Consultant
- At least 2 years of experience in clinical pharmacology
- At least 5 years of experience in GLP QA auditing
- Pharmacology educational background
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