ONCOLOGY RESEARCH COORD II PRN

About the role

Oncology and Research are specialized and require unique skill sets. Realigning our MD Anderson Research Department at Cooper University Health Care with the MD Anderson Cancer Center at Houston’s recommendation, allows research growth in both the structure and the types of studies we are able to offer our clients to advance care. The role of the Oncology Research Coordinator I provides the oversight of clinical studies in the oncology setting managing Quality of Life and specimen trials, while continuing to learn and advance in experience to manage oncology treatment trials. This is an entry level position.

Responsibilities

• Work with sponsors during the study start-up process to prepare the regulatory documents and maintain the studies’ regulatory binders throughout duration of study through close out including version control.
• Work with the Institutional Review Board to submit initial study applications, amendments, continuing reviews, adverse event reports and other submissions.
• Provide regular updates to the Regulatory and Operations team members on where studies are in the review/start-up process, monitoring outcomes, and close out preparation.
• Maintain the delegation of authority logs and regulatory documentation for each study and ensure study staff training on each protocol.
• Work with sponsors to set up site initiation visits, monitoring visits and study close-out visits and prepare post-visit documents.
• Maintain tracking for all protocol related paperwork and collect documents from sponsors for protocol submission and maintenance.
• Coordinate FDA submissions and prepare for all research audits.

Requirements

• 3-5 years of related experience

Qualifications

• Bachelor’s degree preferred

Benefits

• Comprehensive benefits program (health, dental, vision, life, disability, retirement) for full- and part-time employees
• Attractive working conditions
• Opportunities for career growth through professional development