Human Subject Research Coordinator
A Full-time position (40 hrs/wk) in Pediatric Infectious Diseases to conduct surveillance studies and clinical trials. In particular, this individual will be responsible for recruitment and administrative responsibilities for a gastroenteritis and respiratory infection surveillance study under the direction of the Principal Investigator and Health Project Coordinator. This individual will screen and recruit potential study candidates, and perform interviews, data and specimen collection, chart reviews, vaccine verifications, and data entry. This person must work well as part of a team, be able to complete project tasks independently as requested, be comfortable with a variety of data bases, and at all times demonstrate the ability to interact in a professional and positive manner in both verbal and written communications.
JOB DUTIES AND RESPONSIBILITIES:
Screening, recruitment, and monitoring of study subjects .
Screen eligible patients to make sure they meet enrollment criteria. Explain study to parent and obtain informed consent.
Conduct study visits to ensure patient compliance with project protocol
Assist in developing recruitment strategies and monitoring target enrollment numbers.
Identification of subject pool and symptom preview
Interviews with families as required by protocol
Collection, labeling, and coordination of study specimens to be delivered to the laboratory; insure labeling is sequential and interfaces with lab labeling system.
Chart review and information abstraction/recording, phone communications with families/pediatricians/staff, fax/mail as necessary as pertains to enrolled subjects at your site.
Data entry and integrity checks: enter data into web-based database and respond to sponsor data queries as they arise.
Completion of source documents: CRFs, vaccine verifications, and 2-3 follow up phone calls for AGE cohort.
Research Team Collaboration
Attend team meetings and conference calls as needed
Interact with Project Coordinator and Research Lab Director to ensure regulatory and other documents are complete and on time.
Other duties as assigned
Bachelor’s degree and 1 year of experience in human subject research coordination; or equivalent combination of education and experience preferred.
Certified Clinical Research Coordinator and/or nursing degree preferred. Knowledge of software preferred. Experience with specimen collection, labeling and coordination preferred.
Knowledge of word processing and data analysis software preferred.
Candidate must become Human Subjects certified under the HSPP program within the first week of employment required.
The University of Rochester is committed to fostering, cultivating, and preserving a culture of equity, diversity, and inclusion to advance the University’s mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion/creed, sex, sexual orientation, citizenship status, or any other status protected by law. This commitment extends to the administration of our policies, admissions, employment, access, and recruitment of candidates from underrepresented populations, veterans, and persons with disabilities consistent with these values and government contractor Affirmative Action obligations.
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled
Location: School of Medicine & Dentistry
Full/Part Time: Full-Time
Opening: Full Time 40 hours Grade 051
Schedule: 8 AM-4:30 PM