- Bachelor's degree
- or equivalent combination of education and experience (preferred)
- No previous experience
- Or equivalent combination of education and experience eg. an Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee program
- Word processing and data analysis software (preferred)
- Careers
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Human Subject Res Coord II
1 week ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 108 Medicine M&D-Cardiology Div · Schedule · 8 AM-4:30 PM · Responsibilities · Summary: · This position supports the Cardiology Division as a research coordinator in pharmaceutical and device clinical trials. Typical duties will include but ...
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Human Subject Res Coord II
1 week ago
University of Rochester Rochester, United StatesResponsibilities · **Summary:** · This position supports the Cardiology Division as a research coordinator in pharmaceutical and device clinical trials. Typical duties will include but are not limited to: conducting study protocols as the primary coordinator, with responsibility ...
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Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesResponsibilities · **Job summary:** · The University of Rochester Neurorestoration Institute is seeking an individual for the position of Clinical Coordinator. The main role of the Clinical Coordinator will be to operate & maintain the day-to-day operational duties of their assig ...
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Human Subject Res Coord II
3 weeks ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 108 Medicine M&D-Immuno/Rheum Div · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · Using knowledge of Good Clinical Practice standards coordinates, develops, plans, implements, and monitors systems and methods related to human ...
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Human Subject Res Coord I
3 weeks ago
The University of Rochester Rochester, United StatesThe Human Subject Research Coordinator (HSRC) will provide study coordination of a national study with four years to go funded by the Department of Defense (DOD). This study will be in collaboration with study investigators at URMC, academic medical Project Coordinator, Technolog ...
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Human Subject Res Coord II
1 week ago
University of Rochester Rochester, United StatesResponsibilities · **Position Description:** · The Human Subject Research Coordinator will work closely with the Research Manager and respective Principal Investigator(s) to coordinate research studies funded by private industry sponsors. Many research projects include evaluating ...
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Human Subject Res Coord II
1 week ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · We are looking for a research coordinator who is self-motivated, committed to excellence, humble, hardworking, as well as a team player to join the geriatric hematology and oncology team to help improve lives of older adults with blood cancer through researchin ...
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Human Subject Res Coord II
3 weeks ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Using knowledge of Good Clinical Practice standards coordinates, develops, plans, implements, and monitors systems and methods related to human subject research activities. This individual will have responsibility for overseeing administrative processes related ...
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Human Subject Res Coord II
1 week ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours GRange URG 108 Med M&D-Pulmnry/Crit Care Unit · Responsibilities · GENERAL PURPOSE: · The Department of Medicine, Division of Pulmonary Critical Care, at The University of Rochester is seeking a full-time Human Subject Research Specialist, Level II, t ...
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Human Subject Res Coord II
1 week ago
The University of Rochester Rochester, United StatesUsing knowledge of Good Clinical Practice standards coordinates, develops, plans, implements, and monitors systems and methods related to human subject research activities. This individual will have responsibility for overseeing administrative proces Research Coordinator, Clinica ...
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Human Subject Res Coord I
3 weeks ago
University of Rochester Rochester, United StatesOpening · Full Time 40 hours Range URG 106 Dermatology M&D · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · Coordinates the activities associated with human subject research. · SPECIFIC RESPONSIBILITIES:¿¿¿¿¿ · * Coordinates the administrative details required to in ...
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Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Responsible for the implementation and coordination of a prospective and retrospective research study in the Endocrinology Division, including protocol development/revision, patient database management, data input, and synthesis of relevant literature. Work wil ...
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Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · 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, su ...
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Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · This is a position in the Pediatric Infectious Division to assist in pediatric clinical and translational studies, including studies of pediatric COVID-19 vaccines. This person will be responsible for recruitment and have administrative responsibilities, includ ...
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Human Subject Res Coord II
3 weeks ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · The Department of Medicine, Division of Pulmonary Critical Care, at The University of Rochester is seeking a full-time Human Subject Research Specialist, Level II, to coordinate human subject research activities. The division of Pulmonary Critical Care has a ro ...
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Human Subject Res Coord II
1 week ago
University of Rochester Rochester, United StatesResponsibilities · **General Purpose:** · Under general direction and with some latitude for independent judgment for the direction and results of the research, collaborates with the Principal Investigator(s)(PI) and the Ob/Gyn Office of Research Administration to operationalize ...
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Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesResponsibilities · **JOB DESCRIPTION:** · Provide support to the overall coordination of the funded and non-funded clinical studies within EIOH. The individual must be able to work independently with minimal supervision. Excellent interpersonal skills, writing skills, and compute ...
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Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesResponsibilities · **General Purpose:** · The Human Subject Research Coordinator (HSRC) will provide study coordination of a national study with four years to go funded by the Department of Defense (DOD). This study will be in collaboration with study investigators at URMC, acade ...
-
Human Subject Res Coord I
1 week ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Coordinates the activities associated with human subject research. · **SPECIFIC RESPONSIBILITIES:** ¿¿¿¿¿ · + Coordinates the administrative details required to initiate and conduct human subject research, including receiving, distributing and explaining study ...
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Sr Human Subject Res Coord
1 week ago
University of Rochester Rochester, United StatesGENERAL PURPOSE: · Manages and oversees the activities that establish, monitor and maintain human subject research, including responsibility for ensuring proper staff training. Plans, directs, monitors and coordinates all phases of human subject research, which may include multi- ...
Human Subject Res Coord I - Rochester, United States - University of Rochester
Description
ResponsibilitiesGeneral Purpose:
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.
Ensures all immediate and extended team members understand and adhere to all aspects of all approved training manuals, 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.
Keeps current with all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines and makes recommendations.
Other duties as assigned
Qualifications:
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_
Pay Range
Pay Range:
$ $ 26.44 Hourly
_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.
_Apply for Job
Location: School of Medicine & Dentistry
Full/Part Time: Full-Time
Opening: