Remote CRA – Oncology/CAR-T Monitoring

Parexel; Austin (TX); Presencial; USD 70.000 - 110.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Vision insurance

Dental insurance

Tuition reimbursement

Vacation time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Descripción de la vacante

Parexel is seeking a Clinical Research Associate (CRA) with Oncology, Ophthalmology, Metabolic, Hematology or CAR-T monitoring experience to join our Austin team. You will manage clinical sites from identification through closeout, ensuring study quality, patient safety and regulatory compliance.

In this role you will conduct onsite monitoring visits, build site relationships, support enrollment, and ensure data integrity. Strong communication and independent work style are essential.

Formación

• Onsite CRA experience in clinical trials is required.
• Experience in Oncology, Ophthalmology, Metabolic, Hematology or CAR-T monitoring.
• Bachelor-level degree in a health-related discipline.
• Knowledge of GCP and regulatory requirements.
• Experience with CTMS, EDMS, and MS Office.

Responsabilidades

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits.
• Manage site quality and delivery from identification through closeout.
• Serve as primary contact for assigned sites and resolve issues to support study execution.
• Oversee study integrity and relationships with investigators and site staff.
• Review trial performance and safeguard participant rights and safety.

Conocimientos

Site relationship management

Problem solving

Communication

Independence

Client focus

multitasking

Educación

Bachelor's degree in biological science

Herramientas

CTMS

EDMS

Microsoft Office (Excel/Word)

Descripción del empleo

Parexel is seeking a Clinical Research Associate (CRA) with Oncology, Ophthalmology, Metabolic, Hematology or CAR-T monitoring experience to join our Austin team. You will manage clinical sites from identification through closeout, ensuring study quality, patient safety and regulatory compliance.

In this role you will conduct onsite monitoring visits, build site relationships, support enrollment, and ensure data integrity. Strong communication and independent work style are essential.