Research Operations Manager

Ihc Health ServicesMurray, UT
125d$44 - $68

About The Position

This position is responsible for coordinating and overseeing Intermountain Health Research Studies for one or more clinical areas, supporting research initiatives and ongoing efforts. It ensures research staff follow appropriate processes and procedures according to research protocols, good clinical practice guidelines, and FDA regulations. The role involves collaborating with research teams and clinicians on project identification, facilitation of research activities, data collection and analysis, and compliance. The position may serve on various research teams or councils, providing subject matter expertise for scientific review and working alongside clinicians to develop research ideas.

Requirements

  • Eight (8) years of experience coordinating and training in a research, healthcare, academic, or industry setting, OR four (4) years of experience coordinating and training in a healthcare/academic/industry research setting, AND a Bachelor's Degree in a clinical or life science field, business, or healthcare operations.
  • Supervisory, management, or leadership experience.
  • Basic Life Support (BLS) Certification for roles at Primary Children's Hospital.
  • Experience writing manuscripts, SOPs, technical specifications, and managing implementation projects.
  • Demonstrated understanding of data management functions and processes.
  • Ability to travel to various locations.

Nice To Haves

  • Experience in grant-funded projects or clinical trials of relevant field.
  • Experience in a role requiring the ability to demonstrate proficiency with Microsoft and database applications.
  • Experience in study coordination and collaboration.
  • Experience working within a hospital clinical area and/or an understanding of workflows and hospital processes.

Responsibilities

  • Oversee day-to-day operations in one or more designated areas under the direction of the Research Director, including research staff, resources, study participants, and protocol compliance.
  • Provide direction for the technical, protocol-specific, and operational aspects of assigned trials, guiding and supporting the study team to ensure adherence to study objectives, timelines, and budget.
  • Allocate resources for multi-center clinical studies, including protocol review, coordinator assignments, training, education, auditing, and monitoring.
  • Manage departmental and study financials, including budget evaluation and approval.
  • Facilitate training and development for research staff, including but not limited to; Clinical Research Coordinators, Research Nurses, Regulatory Coordinators, Project Coordinators and Research Assistants.
  • Work with stakeholders to ensure timely applications for new studies and lifecycle reporting to sponsors and IRBs.
  • Ensure compliance with policies, regulations, certifications, and good clinical practice, staying current on relevant policies.
  • Develop and maintain documentation tools and data collection instruments.
  • Collaborate on writing reports, research papers, presentations, and articles.
  • Support research staff, including staffing, training, performance management, and career development in collaboration with Research Director.
  • Support strategic initiatives and ensure annual goals are set and met.
  • Drive continuous improvement through performance coaching, career development, and employee engagement.

Benefits

  • Generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness.
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