University of Rochester
Clinical Research Specialist
University of Rochester, Rochester, New York, United States, 14600
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):
255 Crittenden Blvd, Rochester, New York, United States of America, 14642
Opening:
Worker Subtype:
Regular
Time Type:
Time as Reported / Per Diem
Scheduled Weekly Hours:
As Scheduled
Department:
600223 SON Staff/Research Programs
Work Shift:
UR - Day (United States of America)
Range:
UR URG 106 H
Compensation Range:
$21.36 - $29.90
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 PURPOSE
Coordinates the activities associated with human subject research of study enrolling adolescents and young adults admitted to Golisano Children's Hospital diagnosed with an eating disorder. Assumes responsibility for clinical research protocols and timelines. Performs structured work assignments. Coordinates the enrollment of participants to the study. Identifies and documents adverse events per protocol. Performs data collection and data entry activities. Observes for deviations and takes action to minimize them.
ESSENTIAL FUNCTIONS
Assists in the enrollment of participants to the
Disorders of Gut-Brain Interaction and GI Symptoms during Inpatient Nutritional Restoration for Eating Disorders
research study.
Performs chart review and discusses with medical team for pre-screening and eligibility.
Approaches patients and families and conducts informed consent according to study protocol.
Assists in planning study timelines and schedules appointments and study visits.
Assists in data collection procedures including planning and conducting study visit appointments and electronic health record data collection.
Coordinates with medical unit staff and participants to schedule study visits.
Arrives to study unit at designated time and provides study iPad to participants to complete study survey - assisting with questions as needed.
Completes data collection from e-record according to study protocol
Identifies and documents adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
Observes for deviations and takes action to minimize them.
Continues to learn how to recognize and report logistical challenges in protocol implementation to the research team, assisting in resolving challenges
Maintains study data integrity.
Reports deviations when they occur.
Performs quality checks for data accuracy, reports/follows-up with discrepancies.
Maintains all logs, including OnCore system entry and research tabs in the Electronic Medical Record (EMR), according to UR and department Standard Operating Procedures (SOPs).
Complies with Good Clinical Practice and the Code of Federal Regulations.
Keeps current with all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines.
Demonstrates accountability for continuous learning in accordance with Good Clinical Practice standards and guidelines. Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Maintains CITI and Conflict of Interest (COI) certification and renewal as required.
Participates in protocol-related training as required.
Other duties as assigned
MINIMUM EDUCATION & EXPERIENCE
Bachelors degree Required
Or equivalent combination of education and releveant experience Required
KNOWLEDGE, SKILLS AND ABILITIES
Understands and follows simple research protocols and procedures preferred
Fully adheres to applicable safety and/or infection control standards preferred
Understands and follows data integrity standards and processes preferred
Strong interpersonal, communication, and organizational skills preferred
Highly collaborative, ability to work well in a team, fast-paced environment with diverse faculty, staff, students, patients, and families works well in teams preferred
Proficient in MS Office (e.g. Word, Excel, and PowerPoint), REDCap, email, 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.
Notice: If you are a
Current
Employee,
please
log into myURHR
to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward.
Learn. Discover. Heal. Create.
Located in western New York, Rochester is our namesake and our home. One of the world's leading research universities, Rochester has a long tradition of breaking boundaries-always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better.
If you're looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals
At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better-Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.
Job Location (Full Address):
255 Crittenden Blvd, Rochester, New York, United States of America, 14642
Opening:
Worker Subtype:
Regular
Time Type:
Time as Reported / Per Diem
Scheduled Weekly Hours:
As Scheduled
Department:
600223 SON Staff/Research Programs
Work Shift:
UR - Day (United States of America)
Range:
UR URG 106 H
Compensation Range:
$21.36 - $29.90
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 PURPOSE
Coordinates the activities associated with human subject research of study enrolling adolescents and young adults admitted to Golisano Children's Hospital diagnosed with an eating disorder. Assumes responsibility for clinical research protocols and timelines. Performs structured work assignments. Coordinates the enrollment of participants to the study. Identifies and documents adverse events per protocol. Performs data collection and data entry activities. Observes for deviations and takes action to minimize them.
ESSENTIAL FUNCTIONS
Assists in the enrollment of participants to the
Disorders of Gut-Brain Interaction and GI Symptoms during Inpatient Nutritional Restoration for Eating Disorders
research study.
Performs chart review and discusses with medical team for pre-screening and eligibility.
Approaches patients and families and conducts informed consent according to study protocol.
Assists in planning study timelines and schedules appointments and study visits.
Assists in data collection procedures including planning and conducting study visit appointments and electronic health record data collection.
Coordinates with medical unit staff and participants to schedule study visits.
Arrives to study unit at designated time and provides study iPad to participants to complete study survey - assisting with questions as needed.
Completes data collection from e-record according to study protocol
Identifies and documents adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
Observes for deviations and takes action to minimize them.
Continues to learn how to recognize and report logistical challenges in protocol implementation to the research team, assisting in resolving challenges
Maintains study data integrity.
Reports deviations when they occur.
Performs quality checks for data accuracy, reports/follows-up with discrepancies.
Maintains all logs, including OnCore system entry and research tabs in the Electronic Medical Record (EMR), according to UR and department Standard Operating Procedures (SOPs).
Complies with Good Clinical Practice and the Code of Federal Regulations.
Keeps current with all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines.
Demonstrates accountability for continuous learning in accordance with Good Clinical Practice standards and guidelines. Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Maintains CITI and Conflict of Interest (COI) certification and renewal as required.
Participates in protocol-related training as required.
Other duties as assigned
MINIMUM EDUCATION & EXPERIENCE
Bachelors degree Required
Or equivalent combination of education and releveant experience Required
KNOWLEDGE, SKILLS AND ABILITIES
Understands and follows simple research protocols and procedures preferred
Fully adheres to applicable safety and/or infection control standards preferred
Understands and follows data integrity standards and processes preferred
Strong interpersonal, communication, and organizational skills preferred
Highly collaborative, ability to work well in a team, fast-paced environment with diverse faculty, staff, students, patients, and families works well in teams preferred
Proficient in MS Office (e.g. Word, Excel, and PowerPoint), REDCap, email, 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.
Notice: If you are a
Current
Employee,
please
log into myURHR
to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward.
Learn. Discover. Heal. Create.
Located in western New York, Rochester is our namesake and our home. One of the world's leading research universities, Rochester has a long tradition of breaking boundaries-always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better.
If you're looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals
At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better-Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.