Medical University of South Carolina
UNIV - Research Study Coordinator - Hollings Cancer Center
Medical University of South Carolina, Charleston, South Carolina, United States, 29408
Job Description Summary
The Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit are recruiting for a Research Coordinator I.
Entity
Medical University of South Carolina (MUSC - Univ)
Worker Type
Employee
Worker Sub-Type
Classified
Cost Center
CC001332 HCC CTO Administration
Pay Rate Type
Hourly
Pay Grade
University-05
Pay Range
$39,764.00 - $56,670.00 - $73,576.00
Scheduled Weekly Hours
40
Work Shift
Job Description Summary:
Under general supervision of the Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit, this position coordinates, establishes, and supervises complex research protocols at the Hollings Cancer Center (HCC) to efficiently and effectively integrate cooperative group and industry-sponsored trials at MUSC. The role involves promoting awareness of the clinical trial program, exercising judgment on patient management, and ensuring compliance with reporting systems to research bases, NCI, and MUSC staff.
Responsibilities:
Assist Physician Investigators : Identify, consent, screen, enroll eligible patients, and coordinate patient research activities to meet protocol requirements. Screen patients at HCC, inform them about studies, coordinate procedures, ensure protocol compliance, update databases, and participate in multidisciplinary meetings. Facilitate informed consent and coordinate treatment plans and follow-up.
Data Collection and Submission : Collect and submit data accurately and timely to research bases, ensuring data quality, completing case report forms, and managing responsibilities to meet sponsor deadlines.
Adverse Event Reporting : Submit Serious Adverse Events and regulatory reports promptly, ensuring compliance with institutional and sponsor requirements, and addressing protocol deviations within specified timeframes.
Trial Startup Participation : Review new protocols, complete initial and amended Roadmaps, obtain study-specific credentialing, and communicate potential barriers for protocol activation.
Participation in Focus Groups : Attend meetings, present data, maintain protocol information, and contribute to program expansion and trial selection.
Minimum Requirements:
Bachelor's degree and two years of relevant program experience.
Physical Requirements:
Ability to perform various physical activities including standing, sitting, walking, working indoors and outdoors, handling specimens, and visual and auditory functions as detailed in the original description.
If you enjoy working with energetic, enthusiastic individuals, you will find a rewarding career with us!
The MUSC is an Equal Opportunity Employer and participates in the E-Verify program.
#J-18808-Ljbffr
The Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit are recruiting for a Research Coordinator I.
Entity
Medical University of South Carolina (MUSC - Univ)
Worker Type
Employee
Worker Sub-Type
Classified
Cost Center
CC001332 HCC CTO Administration
Pay Rate Type
Hourly
Pay Grade
University-05
Pay Range
$39,764.00 - $56,670.00 - $73,576.00
Scheduled Weekly Hours
40
Work Shift
Job Description Summary:
Under general supervision of the Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit, this position coordinates, establishes, and supervises complex research protocols at the Hollings Cancer Center (HCC) to efficiently and effectively integrate cooperative group and industry-sponsored trials at MUSC. The role involves promoting awareness of the clinical trial program, exercising judgment on patient management, and ensuring compliance with reporting systems to research bases, NCI, and MUSC staff.
Responsibilities:
Assist Physician Investigators : Identify, consent, screen, enroll eligible patients, and coordinate patient research activities to meet protocol requirements. Screen patients at HCC, inform them about studies, coordinate procedures, ensure protocol compliance, update databases, and participate in multidisciplinary meetings. Facilitate informed consent and coordinate treatment plans and follow-up.
Data Collection and Submission : Collect and submit data accurately and timely to research bases, ensuring data quality, completing case report forms, and managing responsibilities to meet sponsor deadlines.
Adverse Event Reporting : Submit Serious Adverse Events and regulatory reports promptly, ensuring compliance with institutional and sponsor requirements, and addressing protocol deviations within specified timeframes.
Trial Startup Participation : Review new protocols, complete initial and amended Roadmaps, obtain study-specific credentialing, and communicate potential barriers for protocol activation.
Participation in Focus Groups : Attend meetings, present data, maintain protocol information, and contribute to program expansion and trial selection.
Minimum Requirements:
Bachelor's degree and two years of relevant program experience.
Physical Requirements:
Ability to perform various physical activities including standing, sitting, walking, working indoors and outdoors, handling specimens, and visual and auditory functions as detailed in the original description.
If you enjoy working with energetic, enthusiastic individuals, you will find a rewarding career with us!
The MUSC is an Equal Opportunity Employer and participates in the E-Verify program.
#J-18808-Ljbffr