Neuroscience Clinical Trials Coordinator II

Atrium Health; Winston-Salem (NC); Presencial; USD 37.000 - 55.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health and welfare benefits

Flexible Spending Accounts

Educational Assistance Program

Descripción de la vacante

Atrium Health is seeking a Study Coordinator to assist in recruiting participants and coordinating NIH-funded clinical studies at the Wake Forest translational neuroscience program. Responsibilities include data collection, scheduling visits, and ensuring protocol compliance within a multidisciplinary team.

The role involves multimodal assessments, including interviews, neuropsychological tests, biospecimen collections, MRI, and medical record abstractions.

Formación

• Excellent interpersonal, oral, and written communication skills.
• Excellent reading comprehension.
• Strong organizational skills.
• EPIC/WakeOne proficiency to include appropriate documentation of research notes.
• Proficient in the use of OnCore/WISER Clinical Trial Management System.
• Basic Computer skills.
• Fosters/promotes a positive image and professional appearance.
• Sensitivity to intercultural relations.
• Sensitivity to the maintenance of confidentiality.
• Knowledge of Microsoft Products.

Responsabilidades

• Works under the direction of the Study Investigators or Clinical Research Nurse Manager with minimal supervision.
• Plays an active role in recruitment of patients to study.
• Performs protocol specific duties required per the research protocol.
• Obtains or assists the Principal Investigator in obtaining informed consent from subjects and reinforces the information that has been provided to subjects and families.
• Fulfills sponsor requirements related to reportable information including adverse events, unanticipated problems, and other information required by the sponsor protocol.
• Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary source documents.
• Identifies and communicates important protocol and data management issues or problems to the supervisor in a timely manner.
• Provides staff relief as required to meet the needs of the department. Participates in scheduled team/department meetings. Participates in quality improvement projects on an on-going basis.
• May mentor new and less experienced staff.
• Follows established Wake Forest Baptist and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan. Practices a high level of integrity and honesty in maintaining confidentiality.
• Performs other related duties as assigned or requested.

Descripción del empleo

Atrium Health is seeking a Study Coordinator to assist in recruiting participants and coordinating NIH-funded clinical studies at the Wake Forest translational neuroscience program. Responsibilities include data collection, scheduling visits, and ensuring protocol compliance within a multidisciplinary team.

The role involves multimodal assessments, including interviews, neuropsychological tests, biospecimen collections, MRI, and medical record abstractions.