Assistant Clinical Research Coordinator
University of California- Irvine
Irvine, CAFull-time
38K–58K a year
Behavioral Health Market Context
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Job Description
re.To be successful in this role, you should have a Bachelor’s degree in a related field, excellent communication and organizational skills, and experience working in a clinical research setting. You should be able to multi-task, prioritize tasks, and effectively use electronic medical record systems. Additionally, you should be comfortable working in a fast-paced environment and have the ability to work both independently and as part of a team. A thorough understanding of clinical research protocols and the ability to remain compliant with them is also essential. If you are an enthusiastic and driven individual looking for a challenging and rewarding opportunity, we would love to hear from you.
University of California- Irvine is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
University of California- Irvine is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Qualifications
- •The ideal candidate will have a passion for research and a dedication to providing excellent patient care.To be successful in this role, you should have a Bachelor’s degree in a related field, excellent communication and organizational skills, and experience working in a clinical research setting
- •You should be able to multi-task, prioritize tasks, and effectively use electronic medical record systems
- •Additionally, you should be comfortable working in a fast-paced environment and have the ability to work both independently and as part of a team
- •A thorough understanding of clinical research protocols and the ability to remain compliant with them is also essential
- •If you are an enthusiastic and driven individual looking for a challenging and rewarding opportunity, we would love to hear from you
Benefits
Responsibilities
- •In this role, you will have the opportunity to work on a variety of clinical research projects and collaborate with our research teams
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