Sup Clinical Research
Wellstar Health Systems

Job Info

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Overview

How would you like to work in a place where your contributions and ideas are valued? A place where you can serve with compassion, pursue excellence and honor every voice? At Wellstar, our mission is simple, yet powerful: to enhance the health and well-being of every person we serve. We are proud to have become a shining example of what's possible when the brightest professionals dedicate themselves to making a difference in the healthcare industry, and in people's lives.
Responsibilities

The Supervisor of the WellStar Research Institute (WRI) has general responsibility to assist in managing clinical trials for the WRI from start-up through close-out. This includes helping with protocol feasibility assessments, site qualification visits and staff management functions. Staff management functions include assisting with daily oversight of staff, staffing/scheduling, performance evaluations, and time keeping. This person will train and provide guidance to the research coordinators, identify and implement corrective action/processes, provide leadership in determining, recommending, and implementing improvements to policies/processes. The Supervisor will also be required to be available to independently manage and coordinate clinical trials and research projects for the WRI
Qualifications

Required Minimum Education: Bachelor's Degree in a related life science or healthcare fieldPreferred Education: Master's Degree in a related life science or healthcare field.

Required Minimum License: N/A

Required Minimum Certification: ACRP-CP, CRC, CRA or CCRP required.

Required Minimum Experience: 5 years related research experience required for a Bachelor's Degree.Preferred Experience: 4 years related research experience required for a Master's Degree.

Required Minimum Skills: Advanced knowledge and understanding of the management and implementation of clinical/translational research operations. Advanced knowledge and understanding of policies, procedures, and regulations governing human subject's research, and stipulations of sponsor contracts or requirements and incorporates them in the conduct of research. Advanced knowledge and understanding of the Federal regulations and guidelines governing the protection of human subjects, e.g., FDA, OHRP, GCP/ICH, and HIPAA regulations. Advanced knowledge of the policies and procedures and requirements of internal departments involved in the approval of research (IRB, grants, contracts, finance, etc.) and the ability to proficiently and compliantly maneuver though the approval processes and assure compliance throughout the research process. Able to conduct multiple studies independently, obtain training or train others to safely and accurately perform or assess required protocol procedures. Works collaboratively with other staff and departments to complete research protocols. Ability to self-direct, exercise appropriate judgment, problem solve and make decisions consistent with WellStar philosophy, goals and objectives. Ability to build credible relationships internally and externally. Possesses ability to communicate, both verbally and in writing, clearly and concisely. Uses effective presentation and meeting techniques (agendas, time management, etc.). Strong computer experience necessary. Strong analytical and problem-solving skills. Excellent interpersonal and organizational skills, good oral and written communication skills.

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