Clinical Data Coordinator — Oncology Trials

The START Center for Cancer Research; San Antonio (TX); Presencial; USD 52.000 - 64.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

401(k) match

Bonus program

PTO & holidays

Medical, dental, vision

Life & disability insurance

FSA/HSA options

EAP program

Supportive culture

Descripción de la vacante

The START Center for Cancer Research in San Antonio, TX is seeking a Data Coordinator to collect, enter, and transmit clinical data for investigational drug studies.

Responsibilities include data entry into CRFs, data quality checks, and coordinating monitor visits; you will work with study teams to obtain records and ensure timely data submission.

Candidates should have a high school diploma and at least two years of clinical data entry experience; CCRP or CCRC credentials are highly desirable.

Formación

• High School Diploma/GED.
• 2 years of clinical data entry experience.
• Knowledge and training in general office administration skills, including computer applications, filing systems.

Responsabilidades

• Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
• Receive and request patient records/data from the study team as required to complete CRFs for assigned studies.
• Review patient data for completeness and accuracy for assigned studies.
• Coordinate and schedule monitor visits for assigned studies, including exit meetings with monitors to review data or queries.
• Identify lab facilities used for assigned studies and communicate to Regulatory Affairs to request lab certifications.
• Review and utilize protocols as guides for study activities for assigned studies.
• Assure that data entry remains current for all assigned studies.
• Attend meetings as required for assigned studies (site initiation, monitor exit, close-out visit, audit preparation).
• Other duties may be assigned at any time.

Conocimientos

Clinical data entry

Data quality checks

Medical terminology

Office software

Educación

Bachelor’s degree

Herramientas

CRF/EDC systems

Descripción del empleo

The START Center for Cancer Research in San Antonio, TX is seeking a Data Coordinator to collect, enter, and transmit clinical data for investigational drug studies.

Responsibilities include data entry into CRFs, data quality checks, and coordinating monitor visits; you will work with study teams to obtain records and ensure timely data submission.

Candidates should have a high school diploma and at least two years of clinical data entry experience; CCRP or CCRC credentials are highly desirable.