Clinical Trials Research Associate - Cancer Center

University of Iowa • Iowa City, IA

42d • Onsite

About The Position

The Holden Comprehensive Cancer Center at the University of Iowa is seeking a Clinical Trials Research Associate to serve as a member of the Clinical Trials Research team to coordinate clinical oncology study activities: assist in the planning, delivery and evaluation of health care provided to research protocol patients; work closely with Clinical Research Coordinators in the collection of data and in close collaboration with multiple departments and offices, including the University Clinical Trials Office; maintain medical documentation, binders and files; manage data entry and electronic data systems for clinical research protocols and laboratory investigations currently being conducted within the Holden Comprehensive Cancer Center (HCCC) at The University of Iowa. The department intends to hire for one position from either Clinical Trials Research Associate, requisition 25004686 or Clinical Trials Research Associate, requisition 25004687, based on the qualifications of the successful candidate. Please apply to the specific position for which you wish to be considered or both. University of Iowa Health Care-recognized as one of the best hospitals in the United States-is Iowa's only comprehensive academic medical center and a regional referral center. Each day more than 12,000 employees, students, and volunteers work together to provide safe, quality health care and excellent service for our patients. Simply stated, our mission is: Changing Medicine. Changing Lives. Holden Comprehensive Cancer Center is Iowa's only NCI-designated comprehensive cancer center. The NCI designation recognized our cancer center, and its research scientist, physicians, and other health care professionals, for their roles in advancing cancer research that impacts on our ability to prevent, detect and treat our patients with cancer. Not just a floor, or a building, or even confined to a single college. Holden Comprehensive Cancer Center coordinates all cancer-related research, education, and patient care by faculty from 41 departments and six colleges, as well as UI Clinics and UI Children's Hospital.

Requirements

• A Masters degree or equivalent combination of education and professional nursing experience.
• 2 years of experience in nursing and/or clinical research.
• Current valid Iowa Registered Nurse license.
• Excellent verbal, written and interpersonal communication skills
• Proficient in computer software applications
• Ability to organize and evaluate complex medical information and data
• Ability to communicate effectively in a team environment
• Ability to manage complex information with attention to detail and a high level of accuracy

Nice To Haves

• Experience with adult oncology patients
• Experience coordinating clinical research studies
• Knowledge of regulatory guidelines and procedures
• Clinical Research Coordinator Certification (SOCRA or ACRP)
• Experience working with Epic
• Experience working with OnCore Clinical Trials Management System
• Knowledge of University of Iowa policies, procedures and regulations

Responsibilities

• Functions as a member of the Clinical Research Services team to plan, deliver, and evaluate the health care provided to research protocol patients.
• Assists in the design, development, execution and administration for protocols and clinical studies.
• Oversees operations of clinical research studies including the recruitment, screening, coordination and scheduling of subject participation and procedures as required by protocol.
• Obtains informed consent; educates study participants on the scope of study, schedule of events per clinical trial protocol and requirements of participation.
• Follows study participants; manages collection of data including maintaining records of patient visits/interviews, documentation of adverse events, and review of medication records. Provides documentation for physician review to ensure patients are screened and treated according to protocol.
• Documents medical histories, symptoms, vital signs, treatments and results for assigned patients according to research protocol; reviews results to ensure quality and accuracy of data gathered; communicates with physician to assist in eligibility determination.
• Monitors compliance, gathers and maintains data for pharmaceutical sponsored research trials, in-house trials and cooperative group studies; develops complex study materials; creates worksheets, treatment flow sheets and assorted tools to ensure accurate source documentation of protocol treatment procedures; triages telephone calls from patients and families to facilitate clinic visits for medical care/emergency care needs; assists in obtaining prescription medications; ensures follow up care is conducted in alignment with clinical trial protocol.
• Collaborates with departments of Radiology, Pathology, Pharmacy, Nursing, Holden Comprehensive Cancer Center, Clinical Research Unit and/or other departments participating in the clinical research to ensure multi-disciplinary patient safety approaches; conveys study specific objectives and requirements; develops communication tools as necessary.
• Enters patients on protocol, ensuring that all prerequisites have been completed and are within the required parameters.
• Serves as liaison to local physicians/hospitals to facilitate care of protocol patients when hospitalized at outside institutions; obtains documentation of the hospitalizations; provides notification to the Principal Investigator, Study Sponsor, and FDA as required per protocol.
• Performs critical analysis of literature relevant to the clinical trials.
• Educates faculty, staff and others about clinical research and methods employed in research studies; prepares educational materials for patients and other staff as needed to carry out protocol therapy.
• Selects, applies and tests standard methodologies, techniques and tools such as manuals, forms and questionnaires.
• Reviews all query reports and resolves all monitoring issues.
• Participates in the development of general goals for the Clinical Trials Support Services
• Ensures time, energy, learning opportunities, and actions are focused on creating a safe, fair and respectful work environment and improving the workplace
• Coaches others on clinical skills, knowledge, and effective individualized patient care.
• Assists in judging validity of data; makes recommendations; performs and interprets statistical analysis of data; prepares data for computer analysis; uses evaluation data to revise and implement change in close collaboration with the principal investigator
• Comply with UI policies and procedures
• Maintain knowledge of departmental SOPs; ensure personal practice is in line with SOPs
• Attends protocol meetings and other University of Iowa Health Care and Study Sponsor meetings; participates on committees as appropriate
• Seeks professional development opportunities
• Maintain primary coordination responsibilities of up to 5 studies actively recruiting patients
• Ability to enroll up to 16 new patients on trial in a calendar year

Benefits

• Regular salaried position located in Iowa City, IA
• Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Educational Services
• Number of Employees: 5,001-10,000 employees