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Clinical Research Operations Leader

2 months ago

Charleston, South Carolina, United States Charleston ENT & Allergy Full time
Clinical Research Manager at Charleston ENT & Allergy

At Charleston ENT & Allergy, we are committed to advancing healthcare through innovative research and patient-centered care. Our mission is rooted in compassion, clarity, and purpose. As a Clinical Research Manager, your contributions will be evaluated through five essential pillars:

  • Exceptional Patient Care: We strive to provide exemplary service and superior care to our patients. This is achieved through our team's steadfast dedication to established protocols and workflows, with a continuous focus on improvement.
  • Team Development and Growth: We prioritize the growth of our team members over mere task management. Our Managers are dedicated to offering ongoing support and constructive feedback, aimed at enhancing both performance and professional development.
  • Continuous Professional Development: We advocate for ongoing growth for our team, both collectively and individually. Creativity is highly valued, and team members are encouraged to share insights that contribute to our collective success.
  • Adaptability and Process Improvement: As a vital part of our organization, our Managers play a key role in navigating a dynamic environment and facilitating the adoption of new workflows and technologies. It is crucial to uphold process integrity across various locations to ensure consistent patient care.

Core Responsibilities of a Clinical Research Manager

  • Evaluate operational, financial, and material requirements for each research project, and develop budgets accordingly. Oversee the acquisition of necessary facilities, equipment, and supplies for successful study execution.
  • Engage in the planning and implementation of research protocols.
  • Formulate and execute strategies for participant recruitment, screening, and retention.
  • Establish robust data collection systems and supervise data processing and documentation in alignment with study protocols.
  • Monitor patient responses, disseminate study findings, and maintain thorough documentation.
  • Facilitate collaboration among investigators, departments, participants, and regulatory bodies. Address challenges and ensure adherence to compliance standards.
  • Oversee the professional development of staff members.

Required Qualifications

  • Previous experience as a Clinical Research Site Manager or a minimum of 3 years as a Clinical Research Coordinator.
  • Proven ability to cultivate a positive workplace atmosphere.
  • Flexibility in adapting to evolving circumstances.
  • Enjoyment of collaborative efforts in a team-oriented environment that values individual contributions and collective achievements.
  • Familiarity with Microsoft applications such as Word, Excel, SharePoint, PowerPoint, Teams, as well as additional software like NextGen EMR, LeadingReach, and Rhinogram is advantageous.