CRA/Sr. CRA US; Remote
Bakersfield, Kern County, California, 93399, USA
Listed on 2026-10-07
-
Healthcare
Clinical Research
Company REV Clinical (formerly CBCC Global Research)
Position CRA/Sr. CRA – Contract to Perm – US
Location United States – Remote
COMPANY BACKGROUNDREV Clinical (formerly CBCC Global Research), headquartered in Bakersfield, California with additional operations in Ahmedabad, India and Australia is a leading, multi-national clinical contract research organization with deep experience in designing and managing clinical trials across a range of therapeutic areas, including Oncology, CNS, and Ophthalmology. REV Clinical provides end-to-end CRO services — spanning clinical study design, project management, data analysis, regulatory strategy and medical writing— across Phase I–IV clinical trials for leading biopharmaceutical companies.
ROLE:CRA/Sr. CRA
As a CRA/Senior CRA, you will support innovative Phase I and II clinical trials while helping expand our capabilities into Phase III and IV programs. This role offers the opportunity to work closely with sponsors, investigators, and leadership while contributing to the growth of REV Clinical. The ideal candidate thrives in a fast-paced, entrepreneurial environment and is passionate about delivering clinical trials with reliability, excellence, and velocity.
KEY RESPONSIBILITIES Clinical Trial Leadership & Execution- Conduct qualification, initiation, monitoring, and closeout visits across the United States
- Ensure compliance with ICH-GCP, FDA regulations, protocols, and SOPs.
- Develop strong relationships with investigators and site personnel.
- Monitor patient safety, data quality, and protocol compliance.
- Support enrollment and site performance initiatives.
- Prepare monitoring reports within required timelines.
- Support audits and inspections.
- Mentor junior CRAs as appropriate.
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- 5+ years of clinical monitoring experience.
- Oncology experience strongly preferred.
- Strong knowledge of ICH-GCP and Australian regulations.
- Must be legally authorized to work in the United States
- Ability to travel extensively throughout the United States
- Oncology clinical trial experience strongly preferred.
- Experience in Neurology, Ophthalmology, or Rare Disease research.
- Global or multi-country study management experience.
- Early-phase (Phase I/II) experience.
Join a rapidly growing global CRO with direct access to senior leadership, meaningful career growth opportunities, diverse therapeutic programs, and the chance to help shape REV Clinical’s growth.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).