Clinical Research Coordinator I
About The Position
Working in the Clinical and Research Program in Pediatric Psychopharmacology The coordinator will contribute to a range of research studies and clinical trials focused on, but not limited to, substance use disorder (SUD) and attention-deficit/hyperactivity disorder (ADHD). Projects include the longitudinal study of outpatient behavioral health patients and examination of impact of stimulants and other treatments in patients with ADHD with and without SUD using electronic health record data. The CRC may also assist on projects focused on comorbid autism spectrum disorder and SUD, as well as projects focusing on transitional aged youth. Specific responsibilities will include recruiting patients for enrollment in studies, administering questionnaires, and completing other activities to support patient assessment and inclusion in trials. Collect, document, analyze and report data. Serve as a liaison with patients and their families and with other hospital departments. Communicate with the Institutional Review Board (IRB) in the submission and updating of protocols and continuing reviews of active studies. Participate in meetings, workshops and department grand rounds. Incumbent must have exceptional organizational skills and a keen attention to detail; excellent verbal and written communication skills; well-developed interpersonal skills and the ability to work well independently as well as with co-workers, peers, and supervisors; ability to effectively and efficiently handle multiple tasks simultaneously with precision and adapt to changes in responsibilities and workloads; and must possess a high degree of integrity and have a strong work ethic.
Requirements
- Exceptional organizational skills and a keen attention to detail
- Excellent verbal and written communication skills
- Well-developed interpersonal skills and the ability to work well independently as well as with co-workers, peers, and supervisors
- Ability to effectively and efficiently handle multiple tasks simultaneously with precision and adapt to changes in responsibilities and workloads
- Must possess a high degree of integrity and have a strong work ethic
Responsibilities
- Recruiting patients for enrollment in studies
- Administering questionnaires
- Completing other activities to support patient assessment and inclusion in trials
- Collect, document, analyze and report data
- Serve as a liaison with patients and their families and with other hospital departments
- Communicate with the Institutional Review Board (IRB) in the submission and updating of protocols and continuing reviews of active studies
- Participate in meetings, workshops and department grand rounds
- Collect & organize patient data
- Maintain records and databases
- Use software programs to generate graphs, reports and slide sets
- Manage the recruitment of patients for research trials
- Monitor the pace and progress of each ongoing study
- Obtain patient study data from medical records, physicians, etc.
- Verify accuracy of study forms
- Update study forms per protocol
- Document patient visits and procedures
- Maintain regulatory binders according to current QA/QC procedures
- Interview study subjects
- Administer and score questionnaires
- Provide basic explanation of study and in some cases obtain informed consent from subjects
- Perform study procedures
- Assist with study regulatory submissions
- Draft consent forms and protocols
- Verify subject inclusion/exclusion criteria
- Assist with manuscript writing and submission
- Perform administrative support duties as required
- Serve as main contact for study collaborators, participants, associated clinics
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
