Oncology Trial Data Specialist

Actalent; New York (NY); Hybrid; USD 34,000 - 48,000; Full time

Job summary

Actalent is seeking a Clinical Research Coordinator (Data) in Bronx, NY, to manage data entry and query resolution for oncology trials. You will support research nurses and physicians by preparing study tools, maintaining records, and ensuring timely reporting of adverse events and study data in line with sponsor and regulatory requirements.

This contract hybrid position emphasizes data quality, source documentation, and regulatory compliance, with responsibilities spanning patient screening,

Qualifications

• 12 years of experience as a Clinical Research Coordinator.
• Extensive oncology clinical research experience, preferably within an NCI-designated cancer setting or similar environment.
• Experience screening, enrolling, and consenting patients into research studies.
• Experience with adverse event reporting, including AE and SAE.
• Proficiency using Oncore for clinical trial management and reporting.
• Proficiency with Excel and Word for creating and maintaining study tools.

Responsibilities

• Coordinate the initiation and activation of new oncology trial protocols before enrollment begins.
• Prepare and maintain study tools, including binders, diaries, checklists, calendars, and flow sheets.
• Use Oncore, Excel, and Word to develop and update study tools and documentation.
• Review patient charts to confirm protocol eligibility and obtain source documents.
• Ensure IRB-approved consent forms are obtained, filed, and provided to patients.

Skills

Clinical Research Coordinator

Data entry

Query resolution

Oncore

AE/SAE reporting

Excel

Word

Tools

Oncore

Microsoft Excel

Microsoft Word

Job description

Actalent is seeking a Clinical Research Coordinator (Data) in Bronx, NY, to manage data entry and query resolution for oncology trials. You will support research nurses and physicians by preparing study tools, maintaining records, and ensuring timely reporting of adverse events and study data in line with sponsor and regulatory requirements.

This contract hybrid position emphasizes data quality, source documentation, and regulatory compliance, with responsibilities spanning patient screening,