- Coordinate research project with investigators, data managers, and clinical staff
- Work with Principal Investigator (PI) and Research Coordinator to update study protocols, protocol amendments, research study measures, and study databases as needed
- Coordinate meetings with study partners, and represent the study at site meetings
- Oversee participant recruitment (working with CBO staff to facilitate participant referrals)
- Oversee adherence to research protocols, including conducting the study informed consent process, maintaining participant confidentiality, and collecting data
- Conduct medical chart reviews
- Conduct research assessments (administering computer and in-person research interviews)
- Coordinate participant tracking, retention and follow up (scheduling participant follow up over the telephone, working with participants and clinic staff to ensure that scheduled study visits take place)
- Coordinate intervention components (e.g., work with CBO on implementation of testing and referral to off-site testing)
- Conduct data entry into electronic databases
- Managing and analyzing data; perform regular audits to ensure that collected data are complete and accurate, and that research protocols are being followed
- Assist with data analysis, drafting reports, preparing conference abstracts, and presentations
- Assist with preparation of grant proposals
- Travel to multiple implementation sites in New York City to oversee study-related activities and facilitate participant recruitment and follow up
- Troubleshoot study-related problems
- Other research related duties as requested
- Bachelor's Degree
- Experience managing research projects preferred
- Experience collecting data for research (e.g. conducting interviews, and extracting medical records) preferred
- Experience in the field of infectious diseases treatment and services, and working with criminal legal system impacted individuals preferred
- As part of a team, must be able to manage multiple tasks and priorities, work independently with minimal supervision, and adhere to study protocol
- Advanced working knowledge of Microsoft Word, ACCESS, and Excel (preferred)
- Excellent interpersonal, organizational, and communication skills
- Fluency in English (and Spanish preferred)
- Experience with writing scientific documents
- Detail oriented
- Knowledge of SPSS, STATA, SAS, or R pre (preferred)
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Study Coordinator - Bronx, United States - Albert Einstein College of Medicine
Description
Study Coordinator
US-NY-Einstein/Resnick - Bronx
Job ID:
Type: Research
# of Openings: 1
Category: Exempt
Albert Einstein College of Medicine
Overview
The study coordinator will work full-time on NIH-funded studies at the intersection of infectious disease and the criminal legal system. Specifically, they will assist with a study comparing the effectiveness of an on-site Point-of-Care COVID-19 testing and education intervention with community health workers (CHWs) as a central component at a community-based organization that provides services to criminal legal system involved individuals in New York City. They may also assist with studies related to HIV and Hepatitis C (HCV) care coordination for individuals who have been released from carceral settings, including a study evaluating the integration of on-site HIV care with CHWS at a reentry organization.
Responsibilities
Position Responsibilities
Qualifications
Qualifications
Skills and Competencies
Hiring Rate:..
Post Probationary Rate:..
Job Rate:..
Minimum Salary Range:USD $58,500.00/Yr.
Maximum Salary Range:USD $58,500.00/Yr.
PI