How You’ll Help Transform Healthcare:

Manages clinical and administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy. Serves as liaison between research sponsors, site management organizations, local Institutional Review Board (IRB), physicians/staff, and R&D.  
 

Recruit, screen, and enroll eligible study participants. Obtain informed consent from study participants.  Manages completion and submission of study related documentation. Communicates with research sponsor or CRO, local or central IRB, Research and Development, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance.  Assist in monitoring enrollment goals.  Coordinates tasks such as developing informed consents and screening materials, scheduling visits, and acting as a liaison between research participants and the research study team. Collects data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.  Collect, process, and ship research specimens as directed in the protocol.  Ensure compliance with study protocol and requirements of regulatory agencies.  Tracks and reports adverse events and protocol deviations. Coordinates all site related monitoring or auditing visits from sponsor or federal agency during the course of the study and at closure. Prepares, submits, and maintains IRB, R&D, FDA and/or any other funding or regulatory documents and research correspondence.  Develops and maintains patient databases and study maintenance logs including but not limited to training logs, delegation of responsibility logs, screening logs, enrollment logs, and investigational product log. Within the scope of their license, perform patient related care independently. Provides in-depth clinical research training and mentorship to junior and intermediate CRC/Ns.  Contributes to trial planning, development, and implementation activities. Provides education and support throughout the research process to all members of the research team and to ancillary departments involved in research. Assists with protocol feasibility determination, identifying potential barriers and proactively solving problems. Assists in developing data collection systems and compiling study-related reports. Assists in writing research grant proposals, manuscripts, study materials, brochures, and correspondence. Acts as a champion for clinical research at Carilion Clinic.  What We Require:

Education: Bachelor’s degree in biology or medical/clinical sciences (i.e. physiology, nursing, etc.), or a related field required. Graduation from an accredited nursing program required. FDA knowledge required. Master’s Degree preferred.

Experience: Minimum of ten (10) years of Clinical Research (or equivalent research experience) ANDa Master’s Degree in Science OR Minimum of fifteen (15) years of Clinical Research (or equivalent research experience)AND a Bachelor’s Degree in Science required.

Licensure/Certifications/Registration: License or certification specific to the discipline according to Virginia requirements. Current license to practice as a Registered Nurse in the Commonwealth of Virginia required.Nationally recognized clinical research certification from Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) required upon hire. I.A.T.A. (International Air Transport Association) certification is required for projects that will be transporting specimens prior to completion of IRB application.

Other Minimum Qualifications: Thorough knowledge of medical terminology and human anatomy and physiology. Working knowledge of the disease/condition under study, the clinical trial process and good clinical practices.  Proficient in the application of federal regulations and the Good Clinical Practices governing clinical research. Must be competent in word processing and spreadsheets. Proficient with data base management systems and statistical software, research methodology, and statistical analysis. Must have effective interpersonal and problem-solving skills. Must be self-directed and excel in attention to detail. Must use good judgment with regard to priorities and deadlines. Must have demonstrated leadership among a research team.

About Carilion

This is Carilion Clinic ...

An organization where innovation happens, collaboration is expected and ideas are valued. A not-for-profit, mission-driven health system built on progress and partnerships. A courageous team that is always learning, never discouraged and forever curious.

Headquartered in Roanoke, Va., you will find a robust system of award winning hospitals, Level 1 and 3 trauma centers, Level 3 NICU, Institute of Orthopedics and Neurosciences, multi-specialty physician practices, and The Virginia Tech Carilion School of Medicine and Research Institute.

Carilion is where you can make your own path, make new discoveries and, most importantly, make a difference. Here, in a place where the air is clean, people are kind and life is good. Make your tomorrow with us.

 

Requisition Number: 151802 
Employment Status: Full time 
Location: CASB - Carilion Administrative Services Building 
Shift: Variable Hours 
Shift Details: 8-5, some later days and weekends
Recruiter: HAYLEY F OHL 
Recruiter Email: hcfield@carilionclinic.org
For more information, contact the HR Service Center at 1-800-599-2537.

Carilion Clinic is an Equal Opportunity Employer: We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, national origin, age (40 or older), disability, genetic information, or veterans status.
Carilion Clinic is a drug-free workplace.