Manager Of Clinical Research

Overview

• Lead clinical research initiatives focusing on oncology trials, driving innovation in cancer detection and treatment methodologies.
• Collaborate with interdisciplinary teams to advance research and enhance patient care through cutting-edge clinical practices.
• Oversee the development and execution of clinical trials, ensuring compliance with regulatory standards and ethical guidelines.
• Manage strategic growth initiatives in clinical research, fostering partnerships with industry sponsors and academic institutions.
• Support grant applications and research programs, contributing to the financial sustainability of clinical research operations.
• Provide leadership and mentorship to research teams, promoting professional development and excellence in clinical research practices.
• Serve as a liaison between internal departments and external collaborators, ensuring seamless communication and coordination.
• Shape the future of oncology care through innovative research and compassionate leadership.

Key Responsibilities & Duties

• Identify and develop new clinical research opportunities aligned with organizational goals and patient needs.
• Oversee the design, implementation, and monitoring of clinical trials, ensuring adherence to protocols and regulatory requirements.
• Collaborate with investigators, faculty, and external sponsors to advance research initiatives and secure funding.
• Ensure compliance with regulatory bodies such as FDA, NIH, and CMS, maintaining high standards of research integrity.
• Support research billing, coding, and financial management to optimize resource allocation and sustainability.
• Develop and implement policies and procedures to enhance the efficiency and effectiveness of clinical research operations.
• Provide strategic direction and oversight for research programs, fostering innovation and excellence.
• Mentor and guide research staff, promoting professional growth and collaboration within the team.

Job Requirements

• Bachelor’s degree in a scientific discipline; Master’s degree preferred.
• Minimum of 5 years of clinical research experience; oncology trial experience preferred.
• Proficiency in clinical trial design, regulatory compliance, and research administration.
• Experience with EPIC, CTMS, or similar systems; knowledge of research billing and finance.
• Preferred certifications: ACRP, SOCRA, HCCA, CIP; RN licensure advantageous.
• Strong project management skills, with experience in policy development and strategic initiatives.
• Ability to collaborate with industry sponsors, academic partners, and regulatory bodies effectively.
• Excellent proficiency in Microsoft Office and general computer applications.