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Clinical Studies Coordinator I, Neurology

Company

Wake Forest Baptist Health
Address , , Nc
Employment type FULL_TIME
Salary
Expires 2023-08-01
Posted at 11 months ago
Job Description

JOB SUMMARY

Under general supervision, responsible for the compilation and collection of data, recruitment of subjects, and general coordination of clinical studies.

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

  • Strong oral, written, and interpersonal communication skills
  • Understanding of medical and/or scientific terminology

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