Clinical Research Associate II, Phase I - California
Quick Summary
Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files,
Responsibilities
~1 min readYou will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
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University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
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1+ years of Clinical Monitoring experience
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Phase I experience
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40-50% overnight travel
The important thing for us is you are comfortable working in an environment that is:
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Work is performed in an office environment with exposure to electrical office equipment.
Frequent travel to clients/ site locations with occasional travel both domestic and international.
Requirements
~1 min readAbility to sit for extended periods and operate a vehicle safely.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Regular and consistent attendance.
Varied hours may be required.
Target Pay Range: $100 - $120K
#LI - Remote
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.
Location & Eligibility
Listing Details
- Posted
- September 21, 2026
- First seen
- September 26, 2026
- Last seen
- September 26, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 37%
- Scored at
- September 26, 2026
Signal breakdown
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