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Clinical Trials Research Assistant
2 months ago
We intend to hire for one position at either the Research Associate, requisition #24003768, or Research Assistant, requisition #24003767, based on the qualifications of the successful candidate.
Please apply to the position you wish to be considered for or both.
Position Responsibilities:
- Clinical Trial Preparation:
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- Aid in the submission of IRB and other committee documents.
- Research Study Visits:
- Perform study procedures.
- Set up for the study visit (prepare lab kits, specialty tests, orders to CRU).
- Project Management:
- Work with other research staff involved in organizing the day-to-day management of the assigned project.
- Perform a variety of routine tasks related to laboratory environment and adhere to safety and compliance guidelines.
About the Stead Family Department of Pediatrics
The Stead Family Department of Pediatrics is a national leader in pediatric medicine. The Department's mission is to provide outstanding care to the children of Iowa and beyond by being a leader in state-of-the-art clinical care to children, performing cutting-edge research to find new treatments and cures for childhood illnesses, and educating the next generation of pediatric health care providers. The Department comprises the medical and research staff of UI Stead Family Children's Hospital. UI Stead Family Children's Hospital is one of the nation's top-ranked pediatric care and research institutions, and Iowa's only comprehensive children's hospital.
Division of Pulmonary Medicine
The Division of Pediatric Pulmonary Medicine is committed to providing outstanding clinical care, education for trainees of all levels, and the advancement of knowledge through the pursuit of biomedical research. Clinical services are provided in the outpatient setting and in the University of Iowa Stead Family Children's Hospital care units. We are regionally and nationally recognized for our expertise.
Education Requirements:
- Bachelor's degree in related field or equivalent combination of education and/or related experience.
- Demonstrated experience in scientific research.
- Demonstrated excellent written, verbal, and interpersonal communication skills.
- Demonstrated proficiency with Microsoft Office and software applications.
- Demonstrated high attention to detail with strong organizational skills.
- Research Professional certification.
- Knowledge of Institutional Review Board procedures, FDA regulations and study sponsor guidelines related to clinical trial research.
- Six months to one year of experience in clinical trial protocol management.
- Demonstrated experience and proficiency with medical terminology.
- Willingness and ability to travel.
Position and Application details:
In order to be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" to the submission:
- Resume
- Cover Letter with which job you are applying for
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 pedsuichildrenshr@healthcare.uiowa.edu
This position is not eligible for University sponsorship for employment authorization.
Additional Information
- Classification Title: Clin Trials Rsrch Asst/Data Mg
- Appointment Type: Professional and Scientific
- Schedule: Full-time
- Work Modality Options: On Campus
- Pay Level: 3A
- Starting Salary Minimum: 41,541
- Starting Salary Maximum: 79,496
- Organization: Healthcare
- Contact Name: Logan Shaw
- Contact Email: pedsuichildrenshr@healthcare.uiowa.edu
The University of Iowa is an equal opportunity/affirmative action employer. All qualified applicants are encouraged to apply and will receive consideration for employment free from discrimination on the basis of race, creed, color, religion, national origin, age, sex, pregnancy (including childbirth and related conditions), disability, genetic information, status as a U.S. veteran, service in the U.S. military, sexual orientation, gender identity, or associational preferences.