DISEASE GROUP SUPERVISOR

LSU; New Orleans (LA); On-site; USD 110,000 - 150,000; Full time

Job summary

LSU Cancer Center is seeking a Disease Group Supervisor to direct and manage designated Disease Groups within the Clinical Trials Office. You will ensure safe, compliant, and efficient conduct of trials and may provide direct patient care per protocol.

The role emphasizes portfolio management, quality, and process improvement in a multidisciplinary environment. Reporting to the CC-CTO leadership, you will supervise Clinical Trial Coordinators and RN CTCs, and serve as a resource on clinical

Qualifications

• Bachelor's degree required with related field.
• 5 years of clinical research experience.
• RN may substitute for Bachelor's with 3 extra years of clinical research experience.

Responsibilities

• Direct and manage designated Disease Groups within the LSU Cancer Center CC-CTO portfolio.
• Ensure safe, compliant, and efficient conduct of clinical trials.
• Supervise CC-CTO Clinical Trial Coordinators and RN CTCs.

Skills

Clinical research experience

Education

Bachelor's degree in Basic or Health Science or related field

Job description

Job Summary/Basic Functions

The Disease Group Supervisor (DGS) will be responsible for directing and managing specified Disease Groups within the LSU Cancer Center Clinical Trials Office (CC-CTO). The Disease Group Supervisor will ensure safe, compliant, efficient, and effective conduct of clinical trials within the disease groups’ portfolio. They will be expected to perform or provide guidance for direct patient care in relationship to study protocol requirements. The DGS will establish, implement, and evolve operational standards, monitor quality and progress, and supervise the CC-CTO Clinical Trial Coordinators (CTC) and RN CTC’s. This position requires a strong emphasis on portfolio management, quality and accountability, and process improvement and growth. The incumbent will work within a multidisciplinary environment with colleagues both internally and externally in a cooperative manner exercising respectfulness and professionalism. They will also serve as a resource regarding clinical research, clinical trial protocols, and compliance for Investigators, Nurses, Pharmacists, Pathologists, Radiologists, and other healthcare personnel involved in the care and management of clinical research patients.

Minimum Qualifications Required

• Education: Bachelor's
• Required Field of Study: Basic or Health Science or related field
• Number of years required to perform the job: 5
• Type of experience required to perform the job: Clinical Research experience
• Substitution: RN may substitute for Bachelor’s with 3 additional years of clinical research experience