Bilingual Research Data Entry & Scheduler

Arizona Liver Health; Tucson (AZ); Sur place; USD 26 000 - 37 000; Plein temps

Avantages offerts par ce poste

Health, Dental, Vision with HSA plans

2 weeks PTO

5 days Sick Time

7 Holidays + 2 Half-days

401K with company match

Short & Long Term Disability

Educational Assistance

Shared company vehicles for travel

Résumé du poste

Arizona Liver Health is seeking qualified candidates for a Research Data Entry/Scheduler (Bilingual) in Tucson. The role supports clinical trials by managing data entry, scheduling, and vendor coordination in a clinical research setting.

Must have a High School Diploma or GED and clinical research experience, with CTMS/EDC proficiency. Full-time, non-exempt position in a clinic setting with comprehensive benefits.

Qualifications

• Excellent communication and problem-solving skills.
• Bilingual Spanish speaking required.
• Ability to multi-task in a fast-paced environment.
• Understand good clinical practice (GCP) and regulatory compliance.

Responsabilités

• Process requests for medical records for study subjects.
• Schedule all necessary procedures and research appointments.
• Liaison with vendors to ensure timely processing.
• Coordinate on-site monitor visits and respond within 48 hours.
• Process subject stipends per ICF and verify monthly payments.
• Communicate stipend/card issues to research subjects professionally.
• Daily and monthly CTMS data reconciliation: unsubmitted visits, unpaid stipends, overdue visits.
• Audit research trials and filing as needed.
• Adhere to IRB approved protocols and SOPs.

Connaissances

Communication skills

Problem solving

Bilingual Spanish

Multi-tasking

Organizational skills

Regulatory compliance

Formation

High School Diploma or GED

Outils

CTMS

EDC program

Description du poste

Arizona Liver Health is seeking qualified candidates for a Research Data Entry/Scheduler (Bilingual) in Tucson. The role supports clinical trials by managing data entry, scheduling, and vendor coordination in a clinical research setting.

Must have a High School Diploma or GED and clinical research experience, with CTMS/EDC proficiency. Full-time, non-exempt position in a clinic setting with comprehensive benefits.