Sup Clinical Research
Company: WellStar Health System
Location: Marietta
Posted on: May 6, 2022
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Job Description:
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 Job
Requirements: 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/ARequired 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.
Keywords: WellStar Health System, Marietta , Sup Clinical Research, Healthcare , Marietta, Georgia
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