Remote Clinical Research Associate (CRA) – Oncology & Beyond

Parexel; Salem (OR); Sur place; USD 70 000 - 95 000; Plein temps

Avantages offerts par ce poste

Health Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Résumé du poste

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

You will conduct onsite monitoring activities, build productive site relationships, address site issues, and support enrollment and study delivery.

Qualifications

• Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of GCP, regulatory requirements, and clinical trial processes.
• Experience using CTMS, EDMS, and Microsoft Office applications.

Responsabilités

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned sites.
• Manage site quality and delivery from site identification through closeout.
• Serve as the primary contact for assigned sites to support study execution.
• Oversee study integrity and build relationships with investigators and staff.
• Review trial performance and safeguard rights, safety, and well-being of participants.

Connaissances

Site relationship management

Problem-solving

Communication skills

Formation

Bachelor's degree in biological science or health-related discipline

Outils

Clinical Trial Management System

Electronic Document Management System

Microsoft Office (Excel/Word)

Description du poste

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

You will conduct onsite monitoring activities, build productive site relationships, address site issues, and support enrollment and study delivery.