University of Rochester
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Clinical Research Coordinator I
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University of Rochester 3 days ago Be among the first 25 applicants Join to apply for the
Clinical Research Coordinator I
role at
University of Rochester 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):
220 Hutchison Rd, Rochester, New York, United States of America, 14620
Opening
Worker Subtype:
Regular
Time Type
Full time
Scheduled Weekly Hours
40
Department
910088 Pediatrics Neonatology
Work Shift
UR - Day (United States of America)
Range
UR URG 102 H
Compensation Range
$17.00 - $22.10
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
GENERAL SUMMARY
Assists with various activities associated with human subject research. Gains knowledge regarding clinical research procedures and protocols. Maintains logs and assists in entering research data into data collection forms and/or study databases.
Essential Functions
Assists with the administrative details required to conduct human subject research. Works under supervision to learn and apply the details of standard protocols, including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form (CRFs) completion, and adverse event reporting. Maintains all logs, including system data entry, according to all pre-established Standard Operating Procedures (SOPs). Assists in entering research data into data collection forms and/or study databases. Practices continuous learning in accordance with Good Clinical Practice (GCP) standards and guidelines. Maintains requisite skills and completes mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Obtains and maintains various certifications applicable to the filed and/or assigned subject matters. Gains knowledge in medical research terminology. Gains and practices proficiency in specific research software needed to manage clinical research protocols. Keeps up to date with new developments in the field by reading related literature and studying relevant clinical standards. May present/share these educational findings with other team members. Participates in protocol-related training as required. Complies with Good Clinical Practice and other applicable regulations. Keeps current with all federal, state, sponsor, and institutional policies, laws, standard operating procedures, and guidelines. Keeps current with industry standards, best practices, and trends in therapeutic areas relevant to research studies.
Other duties as assigned.
Minimum Education & Experience
High School diploma required Associate's degree preferred Or equivalent combination of education and experience
Knowledge, Skills And Abilities
Ability to understand and follow simple research protocols and procedures preferred Ability to adhere to applicable safety and/or infection control standards preferred Ability to understand and follow data integrity standards and processes preferred Strong interpersonal, communication, and organizational skills, and ability to work well in teams preferred Proficiency in Microsoft Office Suite (e.g. Word, Excel, and PowerPoint), email, and internet 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. Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Higher Education Referrals increase your chances of interviewing at University of Rochester by 2x Get notified about new Clinical Research Coordinator jobs in
Rochester, New York Metropolitan Area . Human Subject Research Coordinator Trainee- Part time
Rochester, New York Metropolitan Area $18.65-$26.11 1 month ago Rochester, New York Metropolitan Area $21.36-$29.90 2 weeks ago Rochester, New York Metropolitan Area $21.36-$29.90 1 month ago Rochester, New York Metropolitan Area $21.36-$29.90 2 weeks ago Rochester, New York Metropolitan Area $24.91-$34.87 2 weeks ago Human Subject Research Coordinator Trainee
Rochester, New York Metropolitan Area $18.65-$26.11 1 month ago Rochester, New York Metropolitan Area $24.91-$34.87 2 weeks ago Rochester, New York Metropolitan Area $51,810.00-$72,534.00 1 month ago Rochester, New York Metropolitan Area $24.91-$34.87 1 month ago Rochester, New York Metropolitan Area $51,810.00-$72,534.00 2 weeks ago Clinical Research Coordinator - Rochester General Hospital
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Clinical Research Coordinator I
role at
University of Rochester 3 days ago Be among the first 25 applicants Join to apply for the
Clinical Research Coordinator I
role at
University of Rochester 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):
220 Hutchison Rd, Rochester, New York, United States of America, 14620
Opening
Worker Subtype:
Regular
Time Type
Full time
Scheduled Weekly Hours
40
Department
910088 Pediatrics Neonatology
Work Shift
UR - Day (United States of America)
Range
UR URG 102 H
Compensation Range
$17.00 - $22.10
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
GENERAL SUMMARY
Assists with various activities associated with human subject research. Gains knowledge regarding clinical research procedures and protocols. Maintains logs and assists in entering research data into data collection forms and/or study databases.
Essential Functions
Assists with the administrative details required to conduct human subject research. Works under supervision to learn and apply the details of standard protocols, including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form (CRFs) completion, and adverse event reporting. Maintains all logs, including system data entry, according to all pre-established Standard Operating Procedures (SOPs). Assists in entering research data into data collection forms and/or study databases. Practices continuous learning in accordance with Good Clinical Practice (GCP) standards and guidelines. Maintains requisite skills and completes mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Obtains and maintains various certifications applicable to the filed and/or assigned subject matters. Gains knowledge in medical research terminology. Gains and practices proficiency in specific research software needed to manage clinical research protocols. Keeps up to date with new developments in the field by reading related literature and studying relevant clinical standards. May present/share these educational findings with other team members. Participates in protocol-related training as required. Complies with Good Clinical Practice and other applicable regulations. Keeps current with all federal, state, sponsor, and institutional policies, laws, standard operating procedures, and guidelines. Keeps current with industry standards, best practices, and trends in therapeutic areas relevant to research studies.
Other duties as assigned.
Minimum Education & Experience
High School diploma required Associate's degree preferred Or equivalent combination of education and experience
Knowledge, Skills And Abilities
Ability to understand and follow simple research protocols and procedures preferred Ability to adhere to applicable safety and/or infection control standards preferred Ability to understand and follow data integrity standards and processes preferred Strong interpersonal, communication, and organizational skills, and ability to work well in teams preferred Proficiency in Microsoft Office Suite (e.g. Word, Excel, and PowerPoint), email, and internet 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. Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Higher Education Referrals increase your chances of interviewing at University of Rochester by 2x Get notified about new Clinical Research Coordinator jobs in
Rochester, New York Metropolitan Area . Human Subject Research Coordinator Trainee- Part time
Rochester, New York Metropolitan Area $18.65-$26.11 1 month ago Rochester, New York Metropolitan Area $21.36-$29.90 2 weeks ago Rochester, New York Metropolitan Area $21.36-$29.90 1 month ago Rochester, New York Metropolitan Area $21.36-$29.90 2 weeks ago Rochester, New York Metropolitan Area $24.91-$34.87 2 weeks ago Human Subject Research Coordinator Trainee
Rochester, New York Metropolitan Area $18.65-$26.11 1 month ago Rochester, New York Metropolitan Area $24.91-$34.87 2 weeks ago Rochester, New York Metropolitan Area $51,810.00-$72,534.00 1 month ago Rochester, New York Metropolitan Area $24.91-$34.87 1 month ago Rochester, New York Metropolitan Area $51,810.00-$72,534.00 2 weeks ago Clinical Research Coordinator - Rochester General Hospital
Rochester, NY $70,000.00-$95,000.00 2 weeks ago Part Time - Clinical Robot Associate - Rochester, NY
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr