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Clinical Research Operations Manager

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 a forward-thinking organization committed to advancing healthcare through research and innovation. Our mission is rooted in compassion, clarity, and a dedication to enhancing patient outcomes. As a Clinical Research Manager, your contributions will be measured against our core values:

  • Exceptional Patient Experience: We strive to provide unparalleled service and care to our patients, achieved through our team's steadfast dedication to established processes and a commitment to continuous improvement.
  • Team Development and Empowerment: We prioritize the growth of our team members, offering ongoing support and constructive feedback to foster their professional journeys.
  • Continuous Learning: We promote an environment of ongoing professional development, encouraging creativity and the sharing of insights that contribute to our collective success.
  • Adaptability and Process Improvement: Our Managers play a vital role in navigating the evolving landscape of healthcare, ensuring the implementation of updated workflows and technologies while maintaining the integrity of our processes across various locations.

Key Responsibilities of a Clinical Research Manager

  • Evaluate operational, financial, and material requirements for each research project, and develop comprehensive budgets. Coordinate the acquisition of necessary facilities, equipment, and supplies for successful study execution.
  • Engage in the planning and execution of research protocols.
  • Formulate and implement strategies for participant recruitment, screening, and retention.
  • Establish efficient data collection systems and oversee data management procedures in accordance with study protocols.
  • Monitor participant responses, communicate research findings, and maintain thorough documentation.
  • Facilitate collaboration among investigators, departments, participants, and regulatory bodies, addressing challenges and ensuring compliance.
  • Supervise 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 changing circumstances.
  • Enjoyment in collaborating within a team-oriented environment that values individual contributions and collective achievements.
  • Familiarity with Microsoft tools such as Word, Excel, SharePoint, PowerPoint, Teams, and additional software like NextGen EMR, LeadingReach, and Rhinogram is advantageous.