Clinical Studies Coordinator I, Urology Position Available In Guilford, North Carolina
Tallo's Job Summary: The Clinical Studies Coordinator I position in Urology in Greensboro, NC, involves data compilation, subject recruitment, and study coordination. Requirements include a Bachelor's degree or equivalent experience, medical or research experience, and strong communication skills. Tasks include troubleshooting, data collection, technical procedures, patient recruitment, record maintenance, and report creation. This role may involve supervising volunteers and collaborating with healthcare professionals.
Job Description
Clinical Studies Coordinator I, Urology
Greensboro, NC, United States
Job ID:
153164-OTHLOC-300003371583894
Job Family:
Research Services
Status:
Full Time
Shift:
Day
Job Type:
Regular
Department Name:
35521093333481-Urology
: mail
Overview
JOB SUMMARY
Under general supervision, responsible for thepilation 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 equivalentbination 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 interpersonalmunication 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 forputerization.
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 in.
WORK ENVIRONMENT
Clean, well-lit, office environment andmunity settings
