Clinical Research Associate — Hematology FULL TIME · REMOTE

Karamata Llc; Phoenix (AZ); Híbrido; USD 63.000 - 69.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, dental, and vision coverage

401(k) with employer matching

Paid time off and holidays

Descripción de la vacante

Karamata Llc is seeking a Clinical Research Associate to manage a portfolio of hematology trial sites from qualification to close-out. This hands-on role requires you to stay with source documents, know coordinators, and spot issues a month early.

You will conduct full visit lifecycles, verify data against source records, and ensure patient safety while mentoring junior CRAs as the team grows. Expect ~35% travel across sites in the region.

Formación

• Two or more years of monitoring experience as a Clinical Research Associate.
• Hands-on experience in hematologic malignancies; oncology depth strengthens candidacy.
• A four-year degree, or RN/BSN.
• Written and spoken English at the standard your visit reports will be judged by.
• Organized, exact, and effective without supervision — your sites are yours.
• Fluent across CTMS, EDC platforms, and Microsoft Office.
• Approximately 35% travel.

Responsabilidades

• Conduct the full visit lifecycle — qualification, initiation, interim monitoring, and close-out.
• Verify entered data against source records for accuracy, completeness, and patient safety.
• Review informed consent documentation and subject safety information at every pass.
• Surface protocol deviations early and ensure corrective action.
• Assess and train site staff on protocol adherence where needed.
• Maintain investigational product oversight end to end.
• Keep site documentation flowing into the Trial Master File.
• Mentor newer CRAs with accompanied visits for assessment and training.

Conocimientos

CRA experience

Hematologic oncology

CTMS

EDC

English proficiency

Educación

Bachelor's degree or RN/BSN

Herramientas

CTMS

EDC platforms

Microsoft Office

Descripción del empleo

About the role

You carry a portfolio of hematology trial sites from qualification to close-out, and you own what happens at them. This is a working monitoring role, not an oversight layer: you sit with the source documents, you know the coordinators by name, and when something at a site is about to become a problem, you are the person who saw it a month early.

Responsibilities

• Conduct the full visit lifecycle — qualification, initiation, interim monitoring, and close-out — and manage your sites between visits
• Verify entered data against source records for accuracy, completeness, and patient safety, raising and resolving queries in the EDC
• Review informed consent documentation and subject safety information at every pass
• Surface protocol deviations early, document them plainly, and see corrective action through
• Assess and train site staff on protocol adherence where the site needs it
• Maintain investigational product oversight end to end: receipt, storage conditions, accountability, and return or destruction
• Keep site documentation flowing into the Trial Master File as the study runs, not after it ends
• Mentor newer CRAs — including accompanied visits for assessment and training — as the team grows

Qualifications

• Two or more years of monitoring experience as a Clinical Research Associate
• Hands‑on experience in hematologic malignancies; broader oncology depth strengthens a candidacy
• A four-year degree, or RN/BSN
• Written and spoken English at the standard your visit reports will be judged by
• Organized, exact, and effective without supervision — your sites are yours
• Fluent across CTMS, EDC platforms, and Microsoft Office
• Approximately 35% travel

Pay and benefits

• $46–$50 per hour.
• Medical, dental, and vision coverage;
• 401(k) with employer matching;
• Paid time off and holidays.