| Duties & Responsibilities |
Clinical Research Coordinator, Department of Internal Medicine School of Medicine
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. VCU School of Medicine comprises 18 clinical departments, eight basic health science departments, and 11 affiliated institutes and centers, and provides preeminent education to physicians and scientists in order to improve the quality of healthcare for humanity. 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/ SUMMARY: For
all clinical research studies assigned, the Clinical Research Coordinator is
responsible for coordinating clinical research studies in a compliant and
efficient manner. Under the direction of the Principal Investigator (PI),
collaborate will all members of the clinical research team to ensure all
federal, state, university, and protocol requirements are followed,
institutional research objectives are met, and that ethical obligations are
kept. TYPICAL DUTIES: • Demonstrated understanding of clinical research management duties from
study initiation to close-out.
• Conduct clinical research activities as authorized by the Principal
Investigator’s documented Delegation of Authority and Training Logs.
• Maintain current CITI credentials for Human Subjects Protections, Good
Clinical Practice (GCP), Clinical Research Coordinator, plus additional
sponsor GCP certifications as required.
• Work independently and closely with patients and physicians
• Understand and adhere to all IRB requirements, Human Subjects protection
regulations, and all aspects of IRB approved protocols.
• Conduct all assigned activities in compliance with national, local, &
institutional guidelines, according to all HIPAA, GCP, and other applicable
requirements. Activities include coordinating: new study activation
requirements, screening/enrolling participants, regulatory and compliance
requirements, maintaining appropriate study documentation/records, and
managing study data.
• Ensure patient safety is a top priority in conducting clinical trials.
• Ensure all IRB submissions are complete and submitted on time.
• Maintain regulatory binders in audit ready state- ensuring all
documentation is complete and has been submitted to the IRB.
• Provide timely and courteous responses to queries from patients, faculty
and sponsors.
•Complete and ensure accurate effort reporting is recorded
MINIMUM HIRING STANDARDS: -Demonstrated experience working in and fostering a diverse faculty, staff, and student environment or commitment to do so as a staff member at VCU.
-Demonstrated knowledge and understanding of clinical research management to include: regulatory, human subject’s protection, study conduct, and data management requirements. REQUIRED EDUCATION AND EXPERIENCE: -Excellent communication, writing, and interpersonal skills.
-Exhibits professionalism and ability to work both independently and collaboratively as part of a team; establishing and maintain productive relationships with VCU colleagues and all customers and contacts necessary to effectively support research studies.
-Must be able to prioritize work requirements and multi-task in fast-paced environment, seeking guidance from Principal -Investigators and senior study team staff when necessary.
-Ability to read, interpret, and apply complex regulations, policies, and requirements for each study assigned.
-Excellent organization, time management and critical thinking skills.
-Able to provide own transportation to service areas and meeting locations.
-Participate in professional education and advancement opportunities to facilitate personal and program growth. -Ability to work effectively and collaboratively in a diverse environment required. Preferred Qualifications: - Previous experience as CRC
Preferred Education and Experience: -Previous research experience
-Previous patient care exposure, ideally Nephrology patients
-Familiarity with Cerner strongly preferred
-Degree in a related field or equivalent experience, education, and training Job Specific Physical and Cognitive Requirements:
Light lifting (less than 20 lb), moderate lifting (20-50 lb), fast pace, multiple stimulation, intense customer interaction, frequent change, memory, reasoning, hearing, reading, analyzing, logic, standing, bending, and verbal and written communication.
Additional Information- ORP Eligible: No Hours / weeks - 40 hours weekly
Days /hours - Monday - Friday, Generally 8:00 am - 5:00 pm Title Details:
University Title: Clinical Research Coordinator
University Code: 34111N-34113N
University Job Family: Research
Position will remain open until filled This is a restricted position with no set end date and continued employment
is dependent upon project need, availability of funding, and performance.
A finger print background check is required.
The School of Medicine continuously strives for our workplace and learning
environment to reflect the demographic and social milieu of the communities we
serve. All qualified applicants are encouraged to apply. |
