Staff Research Associate IV, Supervisor

About the role

This position serves as a program manager and senior clinical research coordinator for a large research program. Key responsibilities include overseeing a diverse portfolio of research activities, managing a research team, providing administrative support for clinical trials, and ensuring compliance with regulatory and budgetary requirements.

Responsibilities

• Directly supervises the planning, development, implementation, running, and management of clinical trials at the SFVA Hematology/Oncology Research Program
• Exercises supervisory authority, including hiring, transferring, suspending, promoting, managing conduct and performance, discharging, assigning, rewarding, disciplining, and/or approving hours worked of at least 3 to 6 full-time equivalent (FTE) employees
• Manages, assigns, and performs clinical trial project coordination services for Principal Investigator
• Provides assistance with managing Principal Investigator lab and biospecimen studies and coordinating cross-cutting efforts of bench science with clinical trials
• Contributes to the development of protocols, related documents, manuscripts, and Case Report Forms
• Implements quality assurance standards and compliance in regulatory and budgetary areas of the clinical trials

Requirements

• Master’s degree or Bachelor’s degree with relevant supervisory or budget management experience required
• At least two years of research project management experience and at least two years of employee supervision experience strongly preferred
• At least 2 years of industry trial experience, at least 5 years strongly preferred
• At least 2 years of regulatory work experience in clinical trials, at least 5 years strongly preferred
• Prior experience being part of an academic clinical research group preferred
• Excellent organizational and communication skills (both written and verbal)
• Strong attention to detail
• Flexibility to work both independently and collaboratively

Qualifications

• Knowledgeable of the principles of scientific investigation and clinical trials, capable of in-depth understanding of study protocols

Skills

• Knowledge of project management including tracking, enrollment, retention, regulatory compliance, data management, and staff supervision

Benefits

Not specified

Pay

$70,304.00 - $120,016.00 per year

Schedule

Not specified