We are searching for a motivated Research associate to join our high calibre team at University of Iowa in Iowa City, IA.
Growing your career as a Full Time Research associate is an unparalleled opportunity to develop fundamental skills.
If you are strong in adaptability, attention to detail and have the right determination for the job, then apply for the position of Research associate at University of Iowa today!
Contribute to the success of the Department of Orthopedics and Rehabilitation by conducting clinical orthopedic trauma research with Dr. Mike Willey. This position will conduct and coordinate multicenter clinical trials, with associated reporting and compliance responsibilities. Key areas of responsibility include protocol management and study oversight, subject recruitment and enrollment, data collection and monitoring, and regulatory management. Perform research activities based upon protocols developed by the principal investigator of the research project or other department research staff, working closely with orthopedic residents and medical students on their projects. Screen, recruit, obtain informed consent, and enroll subjects in clinical trials. Educate subjects and their families on study intent, requirements, potential risks and benefits, and possible alternatives. Follow study participants and participate in the collection of data. Assist with dispensing study drug with instructions, monitor compliance, and provide adherence counseling to achieve high compliance standards. Assist in the design, development, execution, and maintenance of data collection forms, questionnaires, and procedure manuals. Prepare regulatory submissions and start-up activities for new studies and maintains regulatory submissions and documentation for ongoing studies. Drafting, formatting, and submitting manuscripts for publication. Prepare bibliographies and abstracts for publications. Read and review articles as directed. As individual skills develop, analyze literature to develop hypothesis for discussion with other researchers or principal investigator. Read and understand protocols. As individual skills develop, troubleshoot and analyze protocols; propose modifications to other researchers or principal investigator. Arrange and plan daily activities to prepare for research protocols. As individual skills develop, perform complex techniques as outlined in research protocols and test and evaluate current procedures. Record and consolidate data as directed by Principal Investigator (PI). Develop databases for study protocols. Perform all data processing tasks and track progress/success of research project. Present results at research meetings. Develop and monitor quality controls. Collect, track, and perform data entry for reports. Prepare materials for reports. As skills develop, analyze data. Serve as a liaison to study sponsors. Position may require some evenings and weekends due to requirements of enrollment protocol. Required Qualifications 2-3 years of experience conducting clinical research. Experience working with statistics and large databases/datasets. Proficient in MS Office computer software applications. Excellent written and verbal communication skills. Attention to detail, ability to multi-task, able to organize priorities, work independently to meet deadlines, and work well within a cohesive team. Experience preparing manuscripts for publication and presentation. Highly Desired Qualifications Grant support (pre award and post award) Experience coordinating multi-center clinical trials, including experience as lead site coordinator. Desired Qualifications Working knowledge of University policies, procedures, and regulations. Experience working with software applications related to research including RedCap. IRB programs, EPIC, DSP, and Excel. Experience with project management. Demonstrated ability to work with a variety of patients. Experience using EPIC for medical chart review and linking subjects to a research study.
Application Process: In order to be considered for an interview, applicants must upload a resume and mark them as a "Relevant File" to the submission.
This position is eligible for a combination of on-campus and remote work. Remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies.
Job openings are posted for a minimum of 14 calendar days and may be removed from posting and filled any time after the original posting period has ended.
Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.
For additional questions, please contact Mike Lucas, View email address on jobs.institutedata.com.
Additional Information Classification Title: Research Associate Appointment Type: Professional and Scientific Schedule: Full-time Work Modality Options: Hybrid within Iowa Compensation Pay Level: 4A
Contact Information Organization: Healthcare Contact Name: Mike Lucas Contact Email: View email address on jobs.institutedata.com Benefits of working as a Research associate in Iowa City, IA:
? Learning opportunities
? Room for Advancement
? Attractive packageCompetitive Pay
? Remote Work opportunity
