Oncology Clinical Data Coordinator

START Research; San Antonio (TX); Vor Ort; USD 40.000 - 60.000; Vollzeit

Benefits dieser Stelle

401(k) match

Annual performance bonus

Paid time off

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA/HSA plans

Collaborative, growth-oriented culture

Zusammenfassung

START Center for Cancer Research invites a Data Coordinator to join our San Antonio team. The role focuses on collecting, entering, and transmitting clinical data for investigational drug studies, with emphasis on accurate CRF completion and data integrity.

Work hours are Monday–Friday, 7:30 a.m.–4:00 p.m. On-site location at 4383 Medical Dr, San Antonio, TX. Collaboration with study teams and compliance with regulatory standards are essential to success in this role.

Qualifikationen

• High School Diploma or GED required.
• Minimum 2 years of clinical data entry experience.
• General office administration skills and computer applications.

Aufgaben

• Collect, enter/transcribe, and transmit/submit clinical data for assigned studies.
• Receive and request patient records/data to complete CRFs.
• Review patient data for completeness and accuracy.
• Coordinate and schedule monitor visits, including exit meetings.
• Identify labs and coordinate with Regulatory Affairs for lab certifications.
• Review protocols and ensure data entry is current.
• Attend study meetings (site initiation, monitor exit, close-out, audit prep).

Kenntnisse

Clinical data entry

General office administration

Ausbildung

High School Diploma/GED

Bachelor’s degree

CCR or CCRC credentials

Jobbeschreibung

START Center for Cancer Research invites a Data Coordinator to join our San Antonio team. The role focuses on collecting, entering, and transmitting clinical data for investigational drug studies, with emphasis on accurate CRF completion and data integrity.

Work hours are Monday–Friday, 7:30 a.m.–4:00 p.m. On-site location at 4383 Medical Dr, San Antonio, TX. Collaboration with study teams and compliance with regulatory standards are essential to success in this role.