Clinical Trials Research Assistant or Associate - Ophthalmology

CLINICAL TRIALS RESEARCH ASSISTANT (PRV1) REQUIRED QUALIFICATIONS

• Bachelor’s degree in science, or health science field related to study, or an equivalent combination of education and experience.
• 6 months to one year of experience in clinical research
• Ability to anticipate needs, problems and potential issues and use judgment, foresight and problem-solving skills to troubleshoot, recommend and implement solutions.
• Demonstrate careful attention to detail and accuracy, strong organizational skills and ability to handle multiple tasks quickly and effectively, proactively establish priorities and meet deadlines.
• Excellent written and verbal communication skills required including ability to compose communications and grammatically correct documents in a concise, logical and organized manner.
• Knowledge of Institutional Review Board procedures, FDA regulations, GCP and study sponsor guidelines related to clinical trial research
• Proficient in computer software applications (Microsoft Office Programs).

CLINICAL TRIALS RESEARCH ASSISTANT (PRV1) DESIRED QUALIFICATIONS

• Knowledge of University policies, procedures, practices, and regulations
• Experience processing expense reimbursements/compensation
• Working with participants and/or patients in a clinical setting
• Basic knowledge of EPIC and electronic medical records
• Six months to one year of experience in clinical trial protocol management
• Six months to one year of experience in data entry and management
• Demonstrated knowledge of or experience with medical terminology
• Basic knowledge of genetics, medical terminology, and disorders 

CLINICAL TRIALS RESEARCH ASSOCIATE (PRV2) REQUIRED QUALIFICATIONS

• Bachelor’s degree in science, or health science field related to study, or an equivalent combination of education and experience.
• Minimum of five (5) years of progressively responsible experience in a research environment 
• Excellent interpersonal, written and verbal communication skills
• Knowledge and experience navigating privacy and confidentiality regulations in human subjects’ research
• Knowledge and experience with conducting clinical trials research, including knowledge of Institutional Review Board procedures, FDA regulations, GCP and study sponsor guidelines related to clinical trial research
• Experience managing Institutional Review Board (IRB) regulatory requirements
• Experience in research data management and database design
• Experience working with participants and/or patients in a clinic setting

CLINICAL TRIALS RESEARCH ASSOCIATE (PRV2) DESIRED QUALIFICATIONS

• Five (5) or more years of progressively responsible experience in the conduct of human subjects’ research
• Active certification as a Certified Clinical Research Coordinator (CCRC) through the ACRP
• Ability to independently design and maintain data collection systems
• Research experience in the fields of ophthalmology and visual sciences
• Experience in research with both minor and adult study participants
• Experience coordinating and scheduling services between multiple departments and/or service providers
• Experience in registry design and implementation
• Experience in research with clinical trials, experimental drug treatments and devices 

POSITION & 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

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. This position is not eligible for University sponsorship for employment authorization.

For additional questions, please contact Melissa Monhollon, HR Manager, at melissa-monhollon@uiowa.edu or 319-356-4674.

The Department of Ophthalmology and Visual Sciences intends to hire either a Clinical Trials Research Assistant (PRA1) or a Clinical Trials Research Associate (PRA2), based on the qualifications of the successful candidate. Please indicate in your application materials the position you wish to be considered for or indicate both.