ALL OPEN ROLES

ALL OPEN ROLES

Clinical Research Associate — Hematology

Clinical Research Associate — Hematology

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.

Between visits you are the site’s day-to-day contact — the one who answers the protocol question before it becomes a deviation, and who escalates obstacles rather than watching them ripen. The record you keep is the trial’s memory: visit reports written as evidence, a TMF that stays current instead of getting reconstructed, data queries driven to resolution rather than logged and forgotten.

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.

ROLE SPECIFICATION

ROLE SPECIFICATION

REQUISITION

REQUISITION

CRA-HEM-01

CRA-HEM-01

FUNCTION

FUNCTION

Clinical Operations — Monitoring

Clinical Operations — Monitoring

EMPLOYMENT TYPE

EMPLOYMENT TYPE

Full time

Full time

LOCATION

LOCATION

Fully Remote - US

Fully Remote - US

TRAVEL

TRAVEL

Approximately 35%

Approximately 35%

REPORTS TO

REPORTS TO

Director, Clinical Operations

Director, Clinical Operations

THERAPEUTIC AREA

THERAPEUTIC AREA

Hematology

Hematology

PHASES

PHASES

II–IV

II–IV

ADDRESS
3101 N. Central Ave. Ste 183 #6830
Phoenix, AZ 85012
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ALL RIGHTS RESERVED.