Senior Clinical Research Coordinator Hematology/Oncology (Contract)

Senior Clinical Research Coordinator – Hematology/Oncology (Contract)

About the Role

We’re looking for a Senior Clinical Research Coordinator (SCRC) to support Hematology/Oncology studies within a high-volume clinical research environment. This role is responsible for managing complex clinical trials from start-up through close-out, ensuring compliance with protocol, regulatory standards, and Good Clinical Practice (GCP).

You’ll work closely with investigators, sponsors, and cross-functional teams to drive enrollment and maintain the integrity of study execution.

Assignment Details

• Schedule: Monday–Friday | 8:30 AM – 5:00 PM
• Duration: 15-week contract
• Work Setting: Fully on-site
• Pay Range: $32–$43/hour

Key Responsibilities

• Independently manage day-to-day clinical trial operations across Hem/Onc studies
• Support patient recruitment, screening, consent, enrollment, and follow-up in a high-enrollment setting
• Ensure strict adherence to protocols, GCP, IRB, FDA, and HIPAA requirements
• Maintain accurate and complete source documentation, regulatory binders, and e-regulatory files
• Collect, review, and enter clinical data into CTMS and study systems, ensuring accuracy and timeliness
• Coordinate study visits, specimen collection, and protocol-driven procedures
• Serve as point of contact for sponsors, CROs, monitors, and investigators
• Facilitate monitoring visits, audits, and investigator meetings
• Drive enrollment targets and study timelines, especially within early-phase trials
• Mentor and support junior research staff and coordinators

Requirements

• Bachelor’s degree and 4+ years of clinical research experience
• (or equivalent combination of education and experience)
• Strong working knowledge of GCP, IRB processes, FDA regulations, and clinical trial protocols
• Hands-on experience with CTMS and electronic regulatory systems
• Ability to manage multiple studies simultaneously in a fast-paced environment

Preferred Background

• Experience in Hematology/Oncology clinical trials
• Exposure to early-phase (Phase I/II) or interventional studies
• Background in pediatric or hospital-based research settings
• Experience working in high-enrollment studies

Core Skills

• Hematology/Oncology Clinical Trials (Interventional & Early Phase)
• GCP & Regulatory Compliance (IRB, FDA, HIPAA)
• Patient Recruitment & Informed Consent
• CTMS & e-Regulatory Documentation
• High-Volume Study Coordination & Data Integrity