<div> 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: <ul> <li>Independently conduct an on-site (at least one week) audit of an executed tox/pharm study.</li> <li>Review reported data against source data for integrity</li> <li>Ensure compliance of data and source systems used to generate data</li> </ul> Ideal Consultant <ul> <li>At least 2 years of experience in clinical pharmacology</li> <li>At least 5 years of experience in GLP QA auditing</li> <li>Pharmacology educational background</li> </ul> </div>

Quality Assurance

Boston Metropolitan Area, USA

Clora is an intelligent platform that matches life science companies with flexible, on-demand expertise. Faster, more cost-efficient, and yields higher quality on-demand talent compared to traditional recruitment methods.

Cambridge, MA, USA

Woburn, MA, USA

Boston, MA, USA

West Street / River Street, Boston, MA, USA

Clora

GLP QA Consultant

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GLP QA Consultant