Clinical Studies Coordinator I -Translational Neuroscience

Responsibilities

• Recruitment, enrollment, and tracking of participants
• Visit scheduling
• Data collection
• Data management and quality assurance
• Regulatory duties
• Supervision of auxiliary staff
• Other relevant administrative tasks

Requirements

• 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.
• 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.
• Aids in the 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.

Qualifications

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

Skills

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

Pay

TBD

Schedule

TBD

Benefits

N/A