Black Diamond client is looking for an experienced clinical (GCP) quality consultant. In this position, you will perform QA oversight activities such as review of site master files, reconciling of TMF, quality review of study activities/clinical study reports, root cause investigations/CAPAs, clinical risk assessments, and other related tasks for the company’s phase I and II solid-tumor investigational therapeutic drugs.
- Minimum 8-10 years of clinical trial site operations-related experience
- Clinical quality/QA experience have strong knowledge of GCP requirements
- Early phase clinical trial experience, preferably oncology (Solid tumor is a plus) experience
Remote: Clinical QA Consultant (227989)