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Clinical Trials Research Assistant - Cancer Center
Company | University of Iowa |
Address | Iowa City, IA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-07-24 |
Posted at | 10 months ago |
Holden Comprehensive Cancer Center is seeking a Clinical Trials Research Assistant to serve as a member of the Clinical Research Services team and 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; perform labs procedures for clinical trials currently being conducted within the Holden Comprehensive Cancer Center (HCCC) at The University of Iowa.
- Attends protocol meetings and other UIHC and Study Sponsor meetings; participates on committees as appropriate
- Properly stores and ships laboratory specimens per study-specific instructions
- Performs ECGs per study protocol
- Enters protocol-required patient data on electronic databases ensuring that all assessments are completed, and data conforms to database required fields
- Reviews patient charts, lab reports, study worksheets and other related information to obtain data required per protocol
- Sponsor Communication
- Submit histology requisitions as required per protocol
- May obtain documentation of external hospitalizations or reports from treatment at external facilities
- Assists in obtaining and delivering prescription medications from investigational pharmacy.
- Assists in the accurate retrieval of basic study data as it pertains to laboratory specimens
- Data Coordination
- Accompanies patients & provide transportation to other departments
- General Responsibilities
- Processes laboratory specimens per study-specific instructions
- Timely Communication regarding gaps in data collection and reporting needs
- May assist in the review of worksheets, treatment flow sheets and assorted tools to provide source documentation of protocol treatment procedures provides follow-up for treatment related complications
- Data Identification & Entry
- Research Team Support
- Assist study coordinators with appropriate tasks as assigned
- Assists in the preparation of research study charts for periodic review by both internal and external monitors. Assist in follow up of any queries identified in the review
- Study Team Support
- Conducts all work in a manner that complies with Institutional Review Board requirements, departmental SOPs, and in response to physician and research needs and requirements
- Maintains the cleanliness, operability, and safety of common lab areas
- Participates in the development of general goals for the Clinical Research Service office
- Maintains, inventories, and orders laboratory kits required per protocol
- Laboratory Functions
- Ability to meet or exceed customer service needs and expectations and provide excellent service in a direct or indirect manner. Ability to effectively transmit and interpret information through appropriate communication with internal and external customers
- Ability to utilize existing resources and learning to achieve or exceed desired outcomes of current and future organizational goals/needs. Able to demonstrate ethical behavior in diverse situations while producing results
- Ability to work with a variety of individuals and groups in a constructive and civil manner while appreciating the unique contribution of individuals from varied cultures, race, creed, color, national origin, age, sex, disability, sexual orientation, and gender identity
- Knowledge of theories and methodologies of medical science research; ability to use research processes, tools and technologies to determine the safety and effectiveness of medical products and services intended for human use
- Knowledge of tools, techniques and resources for obtaining or validating information to be published, exhibited or presented in a variety of methods
- Knowledge of and ability to utilize tools, techniques and processes for gathering and reporting data in a particular department or division of a company
- Knowledge of practices, behaviors, applicable laws, rules, and regulations governing proper research conduct; ability to demonstrate ethical and compliant behavior in diverse situations
- Normal business hours: Monday - Friday 7:00am - 6:00pm
- For more information about Why Iowa?, click here
- Regular salaried position located in Iowa City, Iowa
- Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
- Experience with medical terminology
- Proficient in computer software applications
- Ability to manage complex information with attention to detail and a high level of accuracy
- 6 to 12 months experience in a research or health care setting
- Excellent verbal, written and interpersonal communication skills
- Bachelor’s degree or an equivalent combination of education and experience
- Experience conducting electrocardiograms (ECG)
- Certification that allows for blood draw (Phlebotomy Technician, Certified Medical Assistant, LPN)
- Knowledge of regulatory guidelines and procedures
- Knowledge of University of Iowa policies, procedures and regulations
- Clinical Research Coordinator Certification (SOCRA or ACRP)
- Experience working with Epic
- Relevant experience in the conduct of clinical or laboratory research studies
- Classification Title: Clin Trials Rsrch Asst/Data Mg
- Appointment Type: Professional and Scientific
- Schedule: Full-time
- Pay Level: 3A
- Contact Name: Sarah Waldschmidt
- Contact Email: [email protected]
- Organization: Healthcare
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