Supervisor of Clinical Research

  • Requisition ID: 178065
  • Department: 250701 Clinical Trials Administration
  • Schedule: Full Time - Eligible for Benefits
  • Shift: Day
  • Category: Management

Position Purpose

The Supervisor of Clinical Research serves as clinical and administrative leader that communicates, organizes, prioritizes, leads, facilitates, and problem-solves under the direction of the Director of Clinical Research to enhance access to clinical trials. The incumbent has expert experience in the discipline of clinical research assignment and supervises a specified team in the Renown Research Office as delegated by the Director of Clinical Research. The incumbent is responsible, in collaboration with the Renown Research Office leadership for oversight of all aspects of clinical trials within their assigned specialty area(s) and management of the specialty area(s) to increase the clinical trial portfolio and increase enrollment. The Supervisor of Clinical Research is also responsible for conducting internal audits of clinical trials within the study portfolios of their direct reports, measuring study performance metrics, and implementing action plans, and managing the implementation of assigned departmental initiatives. Additionally, the position requires preceptorship and mentoring of clinical research coordinators, associates, and assistants, and is a resource for all department staff.

 

 

 

Nature and Scope

The incumbent is challenged to provide oversight of the clinical research team and research protocols with an extremely high degree of accuracy, adheres to project timelines, ensures proper quality assurance measures are taken and complies with all regulatory requirements. The Supervisor must stay current on the understanding of all regulations specific to human research subject protections and informed consent. The incumbent must be highly organized, demonstrate technological proficiency, and must also have good interpersonal skills to communicate with research staff, physicians, physician staff, study sponsors, and research participants.

 

This position prepares, submits, and monitors documentation of research program activities while assuring compliance with regulations and protocols. Performs assigned administrative, clinical, and technical duties as directed. Duties include but are not limited to participant and study management, facilitating research team training, implementation and maintenance of department projects, creation of study profiles in all internal research systems including summary and billing information, performing staff evaluations, and supporting staff career development as delegated by the Director of Clinical Research. Completes other work as requested.

 

This position is challenged to manage a large volume of items while maintaining a high degree of accuracy and efficiency with significant attention to detail. Working knowledge of all regulatory requirements governing IRB guidelines. The position requires strong decision-making, independent judgment, and analytical skills in order to apply federal and state regulations to a variety of situations.

 

This position provides patient care.

 

 

Disclaimer

The foregoing description is not intended and should not be construed to be an exhaustive list of all responsibilities, skills and efforts or work conditions associated with the job. It is intended to be an accurate reflection of the general nature and level of the job.

 

 

 

Minimum Qualifications
Requirements - Required and/or Preferred

Name

Description

Education:

Must have working- level knowledge of the English language, including reading, writing, and speaking English. Bachelor of Science in health sciences or bachelor’s degree with 2-year experience in health-related field strongly preferred. 4 years of clinical research experience may substitute for bachelor’s degree.

Experience:

2 years of experience as Clinical Research Coordinator or equivalent position. Previous experience caring for patients on a research protocol. Demonstrated experience in prioritizing and organizing work preferred.

License(s):

Ability to obtain Office Laboratory Assistant credentialing following job-specific training within 6 months of hire.

Certification(s):

AHA BLS certification is required within 90 days of hire.

Human Subject Protection Certificate and GCP Training Certificate required within 90 days or hire.

IATA certification required within 90 days or hire.

CCRP or CCRC preferred within 36 months of hire.

Computer / Typing:

Must be proficient in Microsoft Office Suite, including Outlook, PowerPoint, Excel, Teams, and Word and have the ability to use the computer for online learning requirements for job-specific competencies, access online forms and policies, complete online benefits enrollment, etc.

 

 

Benefits

Renown Health exists to make a genuine difference in the health and well-being of the people and communities we serve. And it is through your passion that this mission is made real every day. The relationship with employees is the foundation for success as we proceed with our strategic direction. We strive to build upon this solid partnership by offering a comprehensive and competitive benefits package that meets the diverse needs of employees and their family members.

With my CAREER Rewards there's peace of mind in knowing that Renown Health is also fighting for the most important things in your life - family, finances and future. Navigate options and make sure you are getting the most value from your Nursing career with us.

  • Icon- Edu Assistance@1x

    Education Assistance

  • Icon - PTO@1x

    Paid Time Off

  • Icon - 401@1x

    401(k) Company Match

  • Icon - Flexible Env@1x

    Flexibile Work Environment