Description:
The Clinical Research Supervisor Non-RN serves this company providing oversight of the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines. The Supervisor is able to function as a clinical study coordinator as needed and serves to train, mentor and develop the clinical study coordinators and research staff in the conduct of clinical research within the AdventHealth research enterprise at the institute level and may extend across multiple U.S. Division locations. Works closely with AHRI Managers and Leaders to facilitate the initiation through completion of clinical research studies in assigned areas. Provides day-to-day supervision and ongoing performance reviews of clinical research staff at the department level. Actively participates in outstanding customer service and accepts responsibility for maintaining relationships that are equally respectful to all.
SUPERVISORY RESPONSIBILITIES
Supervision of a multidisciplinary clinical research operations team
Builds and maintains supportive relationships with each team member through rounding and frequently scheduled connections.
Provides guidance and mentorship to promote growth for study team members, including those in new positions.
Performs a variety of supervisory duties including, but not limited to, leading the Talent Acquisition process of applicant review and selection, support professional and personal team development, and
manages performance management of research team members including positive discipline and Talent Care discussions.
Supervises day-to-day activity of the clinical research team within their assigned area, including oversight of teams productivity and maintenance of personnel and staffing schedules as affected by research protocols at any given time.
Supervises the delivery and delivers safe care with regard for the dignity and respect for all patients/participants.
Serves as a service line expert and resource for the research team when barriers arise during day-to-day operations.
Monitor and evaluate the quality and safety of clinical operations within their assigned area.
Builds and maintains supportive relationships with each team member through rounding and frequently scheduled connections.
Collaborates with operations manager, study intake, research services and external partners to foster a timely start up and smooth transition to assigned coordinator. This is inclusive, but not limited to, review of Medical Coverage Analysis, billing grids, and internal budgeting contribution for time and effort-based modeling. Ensures teams keep an open line of site for maintaining adequate inventory levels, ordering of approved equipment and supplies, maintenance of medical tools (biopsy needles, etc.) and clinical supply areas.
Additional Skills & Qualifications:
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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