Clinical Studies Coordinator Pulmonology Clinic

Atrium Health; Winston-Salem (NC); On-site; USD 52,000 - 68,000; Full time

Job summary

Atrium Health is seeking a Clinical Research Data Coordinator to support the collection and coordination of data for clinical studies. Under general supervision, you will assist in data collection, recruit subjects, and coordinate study activities across teams.

Responsibilities include performing data-related procedures under the PI, maintaining patient records, and communicating with investigators, sponsors, and laboratories to ensure study milestones are met.

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• Experience in a medical and/or research setting.

Responsibilities

• Assist principal investigator and other health professionals in troubleshooting problems related to data management of the clinical study.
• Perform technical procedures on clinical subjects under the direction of the principal investigator or his/her designee.
• Assist with recruitment of patients for the clinical study including tracking the sources of patient referrals.
• Maintain 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, stationary 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.

Skills

Understanding of medical terminology

Strong oral and written communication

Interpersonal skills

Education

Bachelor's degree in related field or equivalent experience

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.

LICENSURE, CERTIFICATION, and/or REGISTRATION

Registered Record Administrator preferred.

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, stationary 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.

Skills/Qualifications

• Understanding of medical and/or scientific terminology


• Strong oral, written, and interpersonal communication skills

WORK ENVIRONMENT

Clean, well-lit, office environment

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