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Job Requirements of Clinical Research Coordinator (Remote):
QUALIFICATIONS / EXPERIENCE:
- General knowledge of the clinical research process, with at least two years of experience in a research setting. An understanding of research design, protocols, and publication submission is expected, as well as clerical experience and the ability to maintain precise record keeping
- Strong computer skills (strong proficiency in Microsoft Office Applications);
- B.A. or equivalent job experience is preferred
- Excellent communication skills
- Excellent organizational skills
- Strong attention to detail with the ability to work in a fast-paced team oriented work environment
- Ability to develop and maintain positive working relationships
- Ability to work independently with speed and accuracy
- Detailed-oriented with efficient time management abilities
- Strong understanding of clinical trials, medical terminology, and the healthcare sector
- Exposure or familiarity with an academic medical setting is a plus
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Clinical Research Coordinator (Remote)
TeamHealth is named among the “150 Great Places to Work in Healthcare” by Becker’s Hospital Review and has ranked three years running as “The World’s Most Admired Companies” by FORTUNE Magazine as well as one of America’s 100 Must Trustworthy Companies by Forbes Magazine in past years. TeamHealth, an established healthcare organizations is physician-led and patient-focused. We continue to grow across the U.S. from our Clinicians to our Corporate Employees and we want you to join us.
*This is a part-time, remote opportunity. Candidates who are located in EST are highly preferred*
JOB DESCRIPTION OVERVIEW:
The Clinical Research Coordinator is responsible for administrative and operationally supporting the director of clinical research and in support of the Morsani School of Medicine Anesthesia Residency Program at Tampa General Hospital. The candidate must have familiarity with clinical research regulatory language, including IRB regulations, as well as an understanding of research protocol descriptions and abstract and publication submissions. Experience or familiarity with EPIC preferred.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Responsible for carrying out duties as directed by research physicians
- Communicate regularly with the designated TeamHealth Supervisor
- Follow and maintain patient confidentiality appropriately with HIPAA compliance standards at all times
- Access hospital information systems or work with facility staff to procure patient demographic and clinical outcomes for research purposes
- Collect data through questionnaires, interviews, charts, and test results
- Assist to enroll subjects and ensure informed consent is properly documented
- Organize data and transfer it from paper to a computer, recorder, or scanner
- Ensure compliance with all clinical trial protocols
- Prepare correspondence, documentation, or presentation materials
- Participate in the development of protocols and case report forms
- Monitor clinical trials and take notes on activities
- Additional tasks or duties as assigned
Job Requirements:
QUALIFICATIONS / EXPERIENCE:
- General knowledge of the clinical research process, with at least two years of experience in a research setting. An understanding of research design, protocols, and publication submission is expected, as well as clerical experience and the ability to maintain precise record keeping
- Strong computer skills (strong proficiency in Microsoft Office Applications);
- B.A. or equivalent job experience is preferred
- Excellent communication skills
- Excellent organizational skills
- Strong attention to detail with the ability to work in a fast-paced team oriented work environment
- Ability to develop and maintain positive working relationships
- Ability to work independently with speed and accuracy
- Detailed-oriented with efficient time management abilities
- Strong understanding of clinical trials, medical terminology, and the healthcare sector
- Exposure or familiarity with an academic medical setting is a plus