Clinical Research Nurse, Downtown Richmond

Virginia Commonwealth University is an equal opportunity, affirmative action university providing access to education and employment without regard to race, color, religion, national origin, age, sex, political affiliation, veteran status, genetic information, sexual orientation, gender identity, gender expression, or disability.

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!

Benefits At a Glance

• Up to 5 remote days per month upon successful completion of training and leadership approval;
• Continuing education and professional development for undergraduate and graduate tuition in addition to mandatory fees (except the transition student fee) for a maximum of six credits per semester;
• 28 University Leave Days, 12+ State Holidays, and 2 Enhanced Community Service Leave Days;
• Medical, Dental and Vision Health Benefits to meet the needs of employees and their eligible family members from the Commonwealth of Virginia as well as optional FSA;
• Participation in the Virginia Retirement System (VRS) and other retirement saving options;
• Parental and Caregiver Leave, Short Term Disability (STD), Disability Insurance, Voluntary Long Term Care Insurance, and Employee Assistance Program;
• Professional development opportunities encouraged and offered for employees as part of annual career development, e.g. certifications, seminars, courses, annual conferences, mentorship, etc.

Massey Comprehensive Cancer Center

Our employees and applicants come from diverse backgrounds. We hire great people from a wide variety of experiences, not just because it’s the right thing to do, but because it makes VCU stronger.

Mission: To reduce the state cancer burden for all Virginians by addressing the confluence between biological, social, and policy drivers through high-impact, cutting-edge research; person-centered care across the continuum, from prevention through survivorship; community integration; and training the next generation of community-centric researchers and healthcare professionals

Vision: To be a premier community-focused cancer center leading the nation in cancer health equity research and ensuring optimal health outcomes for all

Position Primary Purpose and General Responsibilities

A Clinical Research Nurse supports Principal Investigators (PI) in the day-to-day activities required for activation, execution, and management of clinical research studies or protocols. Active clinical licensure is required for duties expected to be directly performed by the Clinical Research Nurse. At Massey, the CRN has more complex and intensive participant contact in a clinical setting requiring an individual with high levels of clinical competency to perform the research related study work. In addition to performing clinical skills associated with research studies, typical duties of a CRN include but are not limited to: assist the 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. A CRN may work independently or as a member of a team. They work under general supervision, resolving most standard issues independently and referring complex issues to an upper-level manager or the PI, as appropriate. The Clinical Trials Office is divided into disease groups within oncology and the CRN would report to the manager of their respective disease group.

• Maintain advanced understanding of clinical research management duties from study initiation to closeout;
• 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 senior 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;
• Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), Clinical Research Coordinator, plus additional sponsor GCP certifications as required;
• Follow VCU internal processes to ensure compliance with VCU policies related to research activities and ensure compliance with federal and state regulatory standards.

Minimum Qualifications

• BSN or equivalent combination of education, experience, and training;
• Current Registered Nursing License in Virginia;
• 2 years’ experience with antineoplastic agent administration, oncology, clinical trials and/or clinical research or equivalent combination of education, experience, and training;
• Intermediate proficiency with Microsoft Excel, Word, Access and Outlook with the ability to adapt to a range of database applications;
• Ability to provide own transportation to meet with patients within the service area;
• Ability to attend meetings within service area and at training locations.

Candidates whose resumes highlight the following previous experience will be prioritized:

• Intermediate proficiency with data entry and word processing skills, with the ability to analyze and interpret information effectively;
• Intermediate organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks;
• Clear and professional written and verbal communication skills, with the ability to interact effectively with colleagues and stakeholders;
• Interpersonal skills, capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts;
• Problem-solving and organizational aptitude, with the ability to manage multiple tasks and meet deadlines in a dynamic environment.

Please note VCU is not able to provide ongoing visa sponsorship for this position.

Please note that if you are employed as a university employee working in any of the health system's facilities, you will need to follow VCU Health System policies, which will include but will not be limited to, vaccination requirements.

Preferred Qualifications

• MSN or equivalent combination of education, experience, and training;
• 4 years’ clinical trial patient care experience or equivalent combination of education, experience, and training including familiarity with federal and state regulatory and clinical research compliance;
• 4 years’ experience with antineoplastic agent administration, oncology, clinical trials and/or clinical research or equivalent combination of education, experience, and training;
• Certification from the Society of Clinical Research Associates (SOCRA), the Association of Clinical Research Professionals (ACRP) or CRA certification for Research Administration;
• 2 years’ experience working in a Clinical Trials Management System (OnCore);
• Collaborative Institutional Training Initiative (CITI) Training or knowledge of regulations regarding the use of human subjects in clinical trials, outcomes research, nursing research, and other research areas or equivalent combination of education, experience, and training;
• Advanced proficiency with Microsoft Excel, Word, Access and Outlook with the ability to adapt to a range of database applications.

Please let us know if you were referred by a current Massey employee to ensure we honor our commitment to the Employee Referral Program.