Study Coordinator

Title: Study Coordinator
Duration: 4 Months CTH (Contract to hire)
Location: Oakland, CA 94609
 
2 years experience with FDA regulated drug trials (MUST HAVE)
Need to be able to work with principle investigators
 
Responsible for coordinating clinical studies including providing administrative support to the research team, including set-up, maintenance of records, serves as the point of contact for study sites and monitors, IRB submission and maintenance of regulatory documents, assisting with enrollment of patients on assigned studies;, data entry and other data management.
Position Requirements:
 
Education: 
 
Bachelor's Degree in relevant scientific discipline or Associates Degree plus two years of Study Coordinator experience.
 
Experience: 
 
Prior intern or paid role in research study in university or health care environment.
 
Skills and Abilities: 
 
Superior communication and organizational skills. Ability to work independently, solve problems, and function calmly and effectively in a hectic environment. Experience with database management. Good writing/editing skills. Microsoft Office Suite, or MAC equivalent.   
 
Physical Requirements:
 
Sit: Up to 8 hours/day 
Stand/Walk: 3-6 hours 
Bend/Stoop: Up to 3 hours 
Reach: Up to 3 hours 
Rep Use of UE/Grasp: Up to 8 hrs 
Lift/Push/Pull: 15 lbs. 
This job requires the ability to hear alarms clients and/or instruction. The ability to see accurately from 20 inches to 20-ft. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential function of this position

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