Clinical Contracts Associate II/Sr.-7587
Do you enjoy research, development, and design? Do you want to build your skillset while working on a team of senior staff clinical researchers? My client, one of the world's largest researchcompanies, is looking to hire a Clinical Research Associate II/Sr. This position is in Tucson, AZ.
This candidate will be responsible for the conduct and management of clinical study activities to verify and validate new clinical software, instrument platforms, assays and biomarkers developed by RMS. Works independently to complete CRA functions associated with study planning, implementation, monitoring and closing study conduct in accordance with the principles of Good Clinical Practice (GCP).
The ideal candidate will possess the following skills:
- BS in biological science with 5+ years of clinical study coordination, clinical site monitoring or clinical study management
- Prior experience with current Good Clinical Practices (cGCP) and Code of Federal Regulations (CFR)
- A background in biomedical/healthcare services with laboratory experience
- PCR, sequencing, and IVD experience preferred
Overall, this is a wonderful opportunity to work on a team and learn from clinical researchers with a thriving company. You will have wide-range of responsibilities and the ability to grow your skill-set.
If you are interested in learning more about the Clinical Research Associate II/Sr. opportunity, please forward me your resume and/or contact me on the details below!
Sthree US is acting as an Employment Business in relation to this vacancy.