Job Details

ID #52609870
Estado Florida
Ciudad Orlando
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-09-30
Fecha 2024-10-01
Fecha tope 2024-11-29
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Clinical Research Supervisor

Florida, Orlando, 32801 Orlando USA
Aplica ya

ShiftMonday-Friday 6:45 AM-3:15 PM Clinical Research SupervisorWill have about 15 direct reports from CRCs, Nurses, and Research Assistants Provide 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 Able to assist with clinical study coordinator duties as needed and serve to train, mentor and develop the clinical study coordinators and research staff in the conduct of clinical research within the research enterprise at the institute level and may extend across multiple U.S. Division locations Provide day-to-day supervision and ongoing performance reviews of clinical research staff at the department level Perform a variety of supervisory duties including, but not limited to, leading the Talent Acquisition process of applicant review and selection, team development and manage performance management of research team members including positive discipline and Talent Care discussions Supervise day-to-day activity of the clinical research team within their assigned area, including oversight of team’s productivity and maintenance of personnel and staffing schedules as affected by research protocols at any given time. Monitor and evaluate the quality and safety of clinical operations within their assigned area Additional duties as needed QualificationsMust have 2 years of clinical research supervisory experience Bachelor’s Degree in Healthcare Administration, Research, or related field and 2 years of experience in clinical research OR Associates degree in Healthcare Administration, Research, or related field and 4 years of experience in clinical research or related field Must be a Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA)) Must hold an active BLS Benefits Benefits from Day One Paid Days Off from Day One Student Loan Repayment Program Career Development Whole Person Wellbeing Resources Mental Health Resources and Support Addiitonal Benefits About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

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