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Job Location (Full Address):
265 Crittenden Blvd, Rochester, New York, United States of America, 14642Opening:
Worker Subtype:
RegularTime Type:
Full timeScheduled Weekly Hours:
40Department:
400081 General PediatricsWork Shift:
UR - Day (United States of America)Range:
UR URG 108Compensation Range:
$51,810.00 - $72,534.00The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
Responsibilities:
GENERAL PURPOSE
The Human Subject Research Specialist II (HSRS II) will coordinate activities associated with all phases of human subject research (project start-up, execution, and closeout) for multiple projects. Under the supervision of the Senior Clinical Trials Project Manager (Sr CTPM), the HSRS II will coordinate quality improvement projects aimed at overcoming vaccination barriers and increasing immunization rates in medical practices, schools, and other community settings. Projects are typically run as randomized controlled trials (RCTs), in which a participating group of sites receives a specific intervention and is then compared to a control/standard-of-care group.
This position requires some weekly on-site work (Saunders Research Building and participating study sites) but allows for partial remote work within the Rochester area if desired. Reliable transportation is needed since the position may require travel to participating schools or medical practices within Monroe and surrounding counties.ESSENTIAL FUNCTIONS
- Oversees and coordinates administrative activities such as the drafting/proofing/editing of regulatory documentation, the drafting/maintenance of subject contact lists and tracking sheets, and dissemination/tracking of subject payment.
- Responsible for the completion of project start up tasks, including the ordering/distribution of recruitment materials, the collection/organization of vaccine rate data, subject (e.g., participating school personnel) outreach, screening, consenting, and the tracking of qualifying participants and sites.
- Schedules and tracks study interviews and regular communication with physicians, nurses and/or staff at participating offices or schools.
- Executes and monitors “training and intervention phase” study activities including the scheduling and/or tracking of online trainings and in-person or virtual meetings/workshops, survey dissemination, and subject payment.
- Assists with the preparation for and execution of training workshop sessions.
- Maintains and audits vaccine rate data as needed to ensure data integrity.
- Completes “post-intervention” activities such as data organization for manuscripts.
- Provides training to student research assistants as needed.
- Actively contributes to weekly/monthly meetings with project Principal Investigator(s), lab manager, project consultants, and advisory board.
- Clearly communicates progress/roadblocks related to study tasks and works both independently and with study team members to solve issues that may arise.
- Actively seeks out and participates in relevant research and/or immunization related trainings and meetings (e.g., SCORE, Pediatric or Public Health Grand Rounds, HRPP Educational Forums, etc.).
- Reads assigned literature to remain current on applicable disease severity and immunization recommendations (as it applies to study goals).
Other duties as assigned
MINIMUM EDUCATION & EXPERIENCE
- Bachelor's degree required.
- 2 years of experience in human subject research coordination required.
- Or equivalent combination of education and experience required.
KNOWLEDGE, SKILLS AND ABILITIES
- Strong communication skills, strong organizational skills required.
- Ability to initiate and complete study related tasks with limited guidance required.
- Proficient at tracking/organizing information in Excel. Experience with REDCap preferred.
LICENSES AND CERTIFICATIONS
- CITI training/certification for human subject research, within 1 month of hire date, required.
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