Oncology Clinical Research Data Coordinator (Hybrid)

Actalent; United States; Híbrido; USD 34.000 - 48.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability insurance

Health Savings Account (HSA)

Transit benefits

Employee Assistance Program

Paid Time Off

Descripción de la vacante

Actalent is seeking an experienced Clinical Research Data Coordinator in Bronx, NY to support oncology trials from initiation through data management. You will prepare study tools, review patient histories, and ensure source documentation aligns with protocol requirements.

The role emphasizes data entry, query resolution, and SAE/AE reporting using Oncore and MS Office tools, with hybrid, contract work from Bronx location.

Formación

• 12+ years as a Clinical Research Coordinator with data entry and query resolution focus in oncology trials.
• Extensive oncology clinical research experience, preferably in an NCI-designated setting.
• Experience screening, enrolling and consenting patients per protocols.
• Experience with AE/SAE reporting and regulatory communications.
• Proficient in Oncore for trial management; skilled in Excel/Word for study tools.

Responsabilidades

• Coordinate initiation and activation of new oncology trial protocols.
• Prepare study tools and binders aligned with protocol requirements.
• Develop and update study tools using Oncore, Excel, and Word.
• Review charts and medical history to confirm eligibility and obtain source documents.
• Ensure IRB-approved consent forms are obtained, filed, and provided to patients.
• Maintain complete research records including CRFs and source documents.
• Assist in grading adverse events using NCI toxicity criteria.
• Complete SAE forms per sponsor, federal regulations, and institutional guidelines.
• Provide status reports to tumor study groups and Principal Investigators on enrollment and data.
• Coordinate sponsor communications and monitoring visits.
• Support screening, enrolling, and consenting per protocols; coordinate medication-related activities.
• Focus on data entry and query resolution; ensure data quality and timelines.
• Support onboarding and training of new coordinators.

Conocimientos

Data entry focus on oncology trials

Query resolution

Oncology clinical research

Adverse event reporting

Trial documentation

Oncore proficiency

Excel proficiency

Word proficiency

Herramientas

Oncore

Excel

Word

Descripción del empleo

Actalent is seeking an experienced Clinical Research Data Coordinator in Bronx, NY to support oncology trials from initiation through data management. You will prepare study tools, review patient histories, and ensure source documentation aligns with protocol requirements.

The role emphasizes data entry, query resolution, and SAE/AE reporting using Oncore and MS Office tools, with hybrid, contract work from Bronx location.