Research Assistant (Oakland) Job at Irvine Clinical Research in Oakland
Behavioral Health Market Context
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Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
argest contributors in the world to the most recently FDA-approved medication in Alzheimer’s Disease.
Oakland Clinical is hiring a Research Assistant who will provide administrative support to our team of doctors and research staff.
This position is designed for an ambitious individual who is willing to start at an entry-level role and work their way up quickly.
Job Duties
• Coordinate the day-to-day clinical operations of a clinical research study
• Perform study procedures in accordance with GCP and study protocols
• Organize and maintain paper and electronic study data in a complete and correct manner
• Recruit, prescreen, and screen potential study participants
• Conduct diagnostic, efficacy, and safety assessments as needed
Job Requirements
• Interest in working with older adults with memory concerns
• Attention to detail and the ability to handle multiple tasks with precision
• Demonstrated ability to work accurately and quickly with computerized systems
• A command of professional spoken and written English
• Bachelor's degree or higher
Hours and Compensation
This is a full-time employment position based in-person at our clinic next to Alta Bates Summit in Oakland.
It is on the 11th floor of a large, safe medical building with transit access, a multi-story parking garage, and beautiful views of the bay.
We have five clinics throughout California, but this is our first site in the San Francisco Bay Area.
The starting salary for this position is approximately $25/hr (approximately $52,000 per year).
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees.
Vacation (PTO) is earned at a rate of 3 weeks per year.
Oakland Clinical is hiring a Research Assistant who will provide administrative support to our team of doctors and research staff.
This position is designed for an ambitious individual who is willing to start at an entry-level role and work their way up quickly.
Job Duties
• Coordinate the day-to-day clinical operations of a clinical research study
• Perform study procedures in accordance with GCP and study protocols
• Organize and maintain paper and electronic study data in a complete and correct manner
• Recruit, prescreen, and screen potential study participants
• Conduct diagnostic, efficacy, and safety assessments as needed
Job Requirements
• Interest in working with older adults with memory concerns
• Attention to detail and the ability to handle multiple tasks with precision
• Demonstrated ability to work accurately and quickly with computerized systems
• A command of professional spoken and written English
• Bachelor's degree or higher
Hours and Compensation
This is a full-time employment position based in-person at our clinic next to Alta Bates Summit in Oakland.
It is on the 11th floor of a large, safe medical building with transit access, a multi-story parking garage, and beautiful views of the bay.
We have five clinics throughout California, but this is our first site in the San Francisco Bay Area.
The starting salary for this position is approximately $25/hr (approximately $52,000 per year).
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees.
Vacation (PTO) is earned at a rate of 3 weeks per year.
Qualifications
- •Interest in working with older adults with memory concerns
- •Attention to detail and the ability to handle multiple tasks with precision
- •Demonstrated ability to work accurately and quickly with computerized systems
- •A command of professional spoken and written English
- •Bachelor's degree or higher
Benefits
- •The starting salary for this position is approximately $25/hr (approximately $52,000 per year)
- •The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees
- •Vacation (PTO) is earned at a rate of 3 weeks per year
Responsibilities
- •This position is designed for an ambitious individual who is willing to start at an entry-level role and work their way up quickly
- •Coordinate the day-to-day clinical operations of a clinical research study
- •Perform study procedures in accordance with GCP and study protocols
- •Organize and maintain paper and electronic study data in a complete and correct manner
- •Recruit, prescreen, and screen potential study participants
- •Conduct diagnostic, efficacy, and safety assessments as needed
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