Clinical Research Associate
Mix Talent · Austin, TX · 2 wk ago
RemoteRemoteResearchFull-time
What You’ll Do
- Conduct site evaluation, initiation, monitoring & closeout visits (on-site + remote)
- Ensure GCP, FDA & ICH compliance
- Review source data, safety reporting & EDC entries
- Oversee IMP accountability & pharmacy compliance
- Support protocol development and study documents
- Mentor junior CRAs and collaborate cross-functionally
What We’re Looking For
- 3+ years CRA experience (on-site + remote)
- Strong GCP & FDA regulatory knowledge
- PREFERRED: CRA monitoring experience within a biotech or biopharma sponsor organization
- Biologics experience a plus
- Willingness to travel up to 50%