What are the responsibilities and job description for the Research Program Coordinator, School of Medicine, Neurology position at Virginia Commonwealth University (VCU)?
Research Program Coordinator, School of Medicine, Neurology | |
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Benefits of working at VCU | All full-time university staff are eligible for VCU’s robust benefits package that includes: comprehensive health benefits, paid annual and holiday leave granted up front, generous tuition benefit, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more. Learn more about VCU’s benefits here. |
Job Code | Clinical Research Coordinator Open (34111N-34116N) |
Recruitment Pool | All Applicants |
Posting Number | req6385 |
Unit | School Of Medicine MBU |
Department | School of Medicine/ Neurology 1590 |
Department Website Link | |
Location | VCU |
Address | 907 Floyd Ave, Richmond, VA 23284 USA |
Duties & Responsibilities | Research Program Coordinator School of Medicine, Neurology Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond. Accounting for almost half of VCU’s sponsored research, the School of Medicine is internationally recognized for patient care and education. All full-time university staff are eligible for our generous benefits package that includes choices for health, vision, and dental coverage, life-insurance, short and long-term disability coverage, retirement planning, tax-deferred annuity and cash match programs, flexible spending accounts, tuition benefits, significant paid-time off, 12 paid holidays, and more. Explore our benefits further here: https://hr.vcu.edu/current-employees/benefits/university-and-academic-professional-benefits/ The Research Program Coordinator will support Principal Investigators (PI) in the day to day activities required for activation, execution, and management of clinical, patient‐oriented research studies or protocols. Typical duties of a Clinical Research Coordinator include, but are not limited to: assist PI in assessing study feasibility, determining participation eligibility, and establishing guidelines for clinical data collection; serve as patient/participant recruiters; and perform a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Maintain established portfolio driven knowledge base of federal and state laws and regulations, sponsor guidance as well as university policies and compliance notices, with ability to consistently interpret and apply accurately. Core Responsibilities: Coordinator work will require maintaining advanced understanding of clinical research management duties from study initiation to closeout. Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), Clinical Research Coordinator, plus additional sponsor GCP certifications as required. Understand and adhere to all IRB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols. Be directly responsible for study coordination and regulatory management of an assigned portfolio of clinical research studies covering a variety of diseases and conditions. Serve as a resource research coordinator for an emerging central coordinator pool; work with leadership to lay the groundwork for expanding a coordinator pool, overall portfolio staffing and management. Serve as an ongoing resource for providing information and expert advice on clinical research issues. Lead the development of best practice guidance and work aids for CRCs in areas such as: study activation, study coordination, data management, and records management. Follow VCU internal processes to ensure compliance with VCU policies related to research activities and ensure compliance with federal and state regulatory standards. Data analyst work will require creation, maintenance and enhancement of the PMDC clinical and research registries/databases and data analysis visualization for grants and publications. Position will require data management including creating framework for data collection, analysis and developing models for analysis and visualization. |
Qualifications | Minimum Hiring Standards: -Bachelors degree or equivalent in data science, biomedical informatics or research management -Minimum of 3 years’ direct experience managing study coordination for industry‐sponsored clinical trials -Minimum of 3 years’ experience in creation, maintenance, and enhancement of clinical and research registries/databases and data analysis visualization Preferred Qualifications: ‐ 5 years relevant professional experience Additional Information: Open Until Filled. This is a restricted position with no set end date and continued employment is dependent upon project needs, availability of funds, and performance. VCU is committed to hiring veterans! VCU will include a veteran's period(s) of military service in the calculation of their annual leave accrual rate. This may provide veterans with an increased leave accrual! |
FLSA | University Employee |
Job FTE | 1 |
Exemption Status | Exempt |
Restricted Position | Yes |
E-Class | UF - University Employee FT |
Job Category | University Employee |
ORP Eligible | No |
Salary Range | Commensurate with Experience up to $85,000 |
Compensation Type | Salaried |
Target Hire Date | 10/11/2024 |
Contact Information for Candidates | Kelly Cecil |
Documents Needed to Apply |
Salary : $85,000