Clinical Studies Coordinator I, Pulmonology, part-time
3 weeks ago
Overview
JOB SUMMARY
Under general supervision, the Clinical Studies Coordinator I is responsible for the compilation and collection of data, recruitment of subjects, and general coordination of clinical studies. This is a part-time, 25 hours a week, position.
EDUCATION/EXPERIENCE
Bachelor's degree in a related field of study or an equivalent combination of experience and education. Experience in a medical and/or research setting. Paramedical experience or other clinical experience.
LICENSURE, CERTIFICATION, and/or REGISTRATION
Registered Record Administrator preferred
SKILLS/QUALIFICATIONS
- Understanding of medical and/or scientific terminology
- Strong oral, written, and interpersonal communication skills
ESSENTIAL FUNCTIONS
- Assists principal investigator and other health professionals in troubleshooting various problems related to the management of the clinical study. Assists in all aspects of the data collection process.
- Performs technical procedures on clinical subjects under the direction of the principal investigator or his/her designee.
- Assists with recruitment of patients for the clinical study including tracking the sources of patient referrals. Follow-up with sources of patient referrals including referring doctors, various Medical Center labs, and other sources.
- Maintains appropriate patient records as necessary. This includes charting the condition of the patient and determining their continued eligibility in the study.
- Obtains and interprets pertinent data from medical records as needed to understand past and present condition of the patients.
- Performs day-to-day administrative and clerical duties such as designing brochures, stationery and data forms. Creates reports and graphs pertinent to the study including presentation of the results of the study.
- May supervise other personnel including volunteers as assigned.
- Assists in development of suitable codes and data collection forms for computerization.
- Consults and cooperates with all faculty, coordination centers, sponsors, and health professionals involved in the clinical study.
- Performs other related duties incidental to the work described herein.
WORK ENVIRONMENT
Clean, well-lit, office environment and community settings
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