Clinical Research Operations Manager

2 weeks ago


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

At Charleston ENT & Allergy, we are a progressive organization committed to advancing healthcare through innovative research and exceptional patient care. Our mission is built on the principles of empathy, transparency, and meaningful impact. As a Clinical Research Manager, your contributions will be evaluated based on our core values:

  • Exceptional Patient Service: We strive to provide unparalleled service and care to our patients. This is achieved through our team's steadfast dedication to established protocols and continuous 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 to enhance the professional journeys of our staff.
  • Continuous Learning: We advocate for ongoing professional development, both as a collective and as individuals. Creativity is encouraged, and team members are empowered to share their insights for collective success.
  • Adaptability and Process Improvement: As integral members of our healthcare organization, our Managers are essential in navigating a changing landscape and supporting the adoption of new workflows and technologies. Maintaining process integrity across various locations is vital for delivering consistent patient care.

Key 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.
  • Design and execute strategies for participant recruitment, screening, and retention.
  • Establish robust data collection systems and supervise data processing and documentation in accordance with study protocols.
  • Monitor patient feedback, communicate research outcomes, 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.

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 work 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 preferred.


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