Top 8 Research coordinator Jobs in Rochester Ny

Human Subject Research Coordinator I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Word processing
- University
- Bachelor's degree
Clinical Research Coordinator, GenoWell Precision Medicine (LPN)
Rochester General Hospital —Rochester, NY
- $63,000 - $80,000 a year
- Full-time
- Nursing
- Mid-level
- Master's degree
Quick Apply
Department Coordinator IV
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Inventory management
- Office
Clinical Research Coordinator II
Iterative Health —Rochester, NY
- $26.50 - $39.00 an hour
- Patient monitoring
- HIPAA
- Mid-level
Quick Apply
10d
Project Coordinator
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Weekends as needed
- Word processing
- Mid-level
- Driver's License
Human Subjects Research Coordinator- II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Weekends as needed
- Mid-level
- Windows
- University
Human Subjects Research Coordinator II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Management
- Word processing
- Mid-level

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Clinical Research Coordinator, GenoWell Precision Medicine (LPN)
Rochester General Hospital —Rochester, NY
Associate’s (or practical nurse diploma) degree in a health related field and 4+ years of experience in either clinical practice or research studies required.
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Human Subject Research Coordinator I

University of Rochester -
Rochester, NY

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Job Details

Full-time
$21.78 - $30.53 an hour

Qualifications

Informed consent
Research ethical considerations
Adverse event reporting
Clinical incident reports
Word processing
Regulatory reporting
Medication adherence support
Clinical research protocol review
Research project coordination
Data integrity and documentation
Clinical staff training
Bachelor's degree
Clinical training
Team training
Data Security (Data management)
Informed consent procedures implementation
Document review
Clinical trial standard operating procedures
Telephone interviewing
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
Communication with regulatory authorities for clinical trials
Clinical research inspection readiness
Clinical quality assurance standards
IRB compliance
1 year
Research participation
Standard operating procedures (SOPs)
Communication skills

Full Job Description

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.

Job Location (Full Address):

601 Elmwood Ave, Rochester, New York, United States of America, 14642

Opening:

Worker Subtype:

Regular

Time Type:

Full time

Scheduled Weekly Hours:

Department:

400087 Pediatrics M&D Inf Diseases

Work Shift:

UR - Rotating (United States of America)

Range:

UR URG 106 H

Compensation Range:

$21.78 - $30.53

The 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:

Coordinates the activities associated with human subject research.

RESPONSIBILITIES:

Coordinates the administrative details required to initiate and conduct human subject research, including receiving, distributing and explaining study information, such as protocol and human subject recruitment materials, to immediate team members and relevant others.

Assists in human subject recruitment and screening activities, including reviewing study site patient databases and office records for patients that meet the protocol inclusion criteria. May participate in developing recruitment strategies. May conduct telephone interviews to screen potential study candidates. Reviews medical chart history with Principal Investigator to verify inclusion criteria are met before enrollment.

Conducts visits to ensure research participant adherence with protocol requirements, such as taking of medications, proper use of device, and/or other interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board (IRB), Sponsor, and/or any other required recipients or entities. Ensures all data are collected and secured within approved parameters and procedures.

Ensures all immediate and extended team members understand and adhere to all aspects of all approved protocols, procedures, and standards for documentation and communication. Under general direction from the Principal Investigator (PI), trains staff on details of protocol, including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form (CRFs) completion, and adverse event reporting.

Reviews and documents the dispensing and returning of study materials, such as study drugs and devices. Ensures additional training is provided to ensure changes to protocol and documents are communicated and adhered to.

Acts as liaison with Sponsor's Monitor to provide data clarifications, reviews study protocols, ensures thorough understanding and communication, responds to questions that arise during the study, communicates and documents adverse events as advised by the PI and ensures regulatory and other documents, such as consent forms and CRFs, are complete, accurate, and available for review. Communicates with Sponsor to clarify data queries to determine report format. Prepares for, participates in, and serves as liaison for scheduled Sponsor monitoring visits (i.e. pre-study inspection, initiation, on-going and close out visits).

Keeps current with all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines and makes recommendations. Demonstrates accountability for continuous learning in accordance with Good Clinical Practice standards and guidelines. Keeps current with industry standards, best practices, and trends in therapeutic areas relevant to research studies. Makes recommendations and implements changes as appropriate.

QUALIFICATIONS:

Bachelor's degree required

1 year of experience in human subject research coordination required

or equivalent combination of education and experience required

Word processing and data analysis software preferred

The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture 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 characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.

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Refine Your Search

research coordinator jobs in rochester ny

Human Subject Research Coordinator I

Clinical Research Coordinator, GenoWell Precision Medicine (LPN)

Department Coordinator IV

Clinical Research Coordinator II

Project Coordinator

Human Subjects Research Coordinator- II

Human Subjects Research Coordinator II

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