Clinical Research Data Spec I
4 weeks ago
Opening
Full Time 40 hours Range URG 106 Surgery-Cancer Control
Schedule
8 AM-5 PM
Responsibilities
GENERAL PURPOSE:
The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree of accuracy, the ability to exercise some independent judgment, flexibility to vary specific tasks as needed and maintain strict adherence to HIPAA requirements and federal, University and division data quality assurance and quality control standards. Requires collaboration with other research team personnel (investigators, health project coordinators, data managers, analyst programmers, biostatisticians).
JOB DUTIES AND RESPONSIBILITIES:
* Logs in and performs thorough review of high-volume incoming research data for multiple studies for accuracy and completeness, and determines if data queries are necessary. Queries off-site coordinators for missing and incomplete data.
* Performs thorough examination of all data entered into Access and REDCap databases for clarity and accuracy.
* Working closely with investigators, designs/creates scannable (TeleformTM) versions of study questionnaires. Troubleshoots areas of common incomplete and faulty data and suggests improvements in flow of information, error detection/correction, etc.
* Assists in designing/preparing study packets for patients, data submission cover sheets, and other study-related items as necessary, e.g., pharmacy manuals, training manuals.
* Prepares, ships, and tracks study supplies to multiple off-site locations.
* Works closely with investigators and study personnel, as well as on-site study coordinators to develop appropriate data collection methods for each research project. Analyzes and suggests improvements in flow of information, error detection/correction, etc.
* Creates electronic data tracking forms and electronic participant charts.
Other duties as assigned
QUALIFICATIONS:
* Associate's degree required
* Bachelor's degree preferred
* 1 year of relevant experience required;
* or equivalent combination of education and experience required
Preferred:
* Skill in completing assignments accurately and with attention to detail required
* Ability to process and handle confidential information with discretion required
* Commitment to the University's core values required
* Ability to work independently and/or in a collaborative environment required
* Understands and follows data integrity standards and processes required
* Strong interpersonal, communication, and organizational skills required
* Highly collaborative, works well in teams required
* Proficient in MS Office (e.g. Word, Excel, and PowerPoint), email, internet required
* Ability to understand and follow standard research protocols and procedures preferred
* Knowledge of medical terminology preferred
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: $20.92 - $29.29 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.
-
Clinical Research Data Spec I
4 weeks ago
Rochester, United States University of Rochester Full timeGENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Under supervision from these senior level staff, coordinates with the investigational...
-
Clinical Research Data Spec I
4 weeks ago
Rochester, United States University of Rochester Full timeOpening Full Time 40 hours Range URG 106 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department...
-
Clinical Research Data Spec I
3 weeks ago
Rochester, United States University of Rochester Full timeOpening Full Time 40 hours Range URG 106 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department...
-
Clinical Research Data Spec I
3 weeks ago
Rochester, United States University of Rochester Full timeGENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Under supervision from these senior level staff, coordinates with the investigational...
-
Clinical Research Data Spec I
2 months ago
Rochester, United States The University of Rochester Full timeUnder the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating proced Clinical Research, Clinical, Research, Data, Monitoring, Management, Technology
-
Clinical Research Data Spec I
4 weeks ago
Rochester, United States University of Rochester Full timeGENERAL PURPOSE: The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree of accuracy, the ability to exercise some independent judgment, flexibility to vary specific tasks as...
-
Clinical Research Data Spec I
2 weeks ago
Rochester, United States University of Rochester Full timeGENERAL PURPOSE: The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree of accuracy, the ability to exercise some independent judgment, flexibility to vary specific tasks as...
-
Human Subject Research Spec I
2 months ago
Rochester, United States The University of Rochester Full timeHuman Subject Research Spec I Next Job Apply for Job When you are ready to apply, registering only takes a minute. Your online account allows you to upload your resume or CV, apply for jobs and access our online career tools. For general questions ab Research, Technology, Education
-
Human Subject Research Spec I
2 months ago
Rochester, United States The University of Rochester Full timeThis is a full-time position (40 hrs/wk) in Ob/ Gyn to conduct clinical research studies. In particular this individual will be responsible for recruitment and administrative responsibilities for several studies under the direction of the Principal I Clinical Research, Research, Data Entry, Research Coordinator, Operations, Technology, Education
-
Human Subject Research Spec I
3 weeks ago
Rochester, United States The University of Rochester Full timeThis is a full-time position (40 hrs/wk) in Ob/ Gyn to conduct clinical research studies. In particular this individual will be responsible for recruitment and administrative responsibilities for several studies under the direction of the Principal I Clinical Research, Research, Data Entry, Research Coordinator, Operations, Technology, Education
-
Human Subject Research Spec I
2 weeks ago
Rochester, United States The University of Rochester Full timeHuman Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated with human subject research. They will work under the supervision and guidance of the Principal Investigator (P Clinical Research, Research Coordinator, Research, Technology, Clinical
-
Human Subject Research Spec I
5 days ago
Rochester, New York, United States The University of Rochester Full timeHuman Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated with human subject research. They will work under the supervision and guidance of the Principal Investigator (P Clinical Research, Research Coordinator, Research, Technology, Clinical
-
Clinical Trials Proj Spec I A
1 month ago
Rochester, United States The University of Rochester Full timeThe responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the c Clinical, Clinical Research, Project Coordinator, Team Leader, Healthcare, Education
-
Clinical Trials Proj Spec I A
4 days ago
Rochester, New York, United States The University of Rochester Full timeThe responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the c Clinical, Clinical Research, Project Coordinator, Team Leader, Healthcare, Education
-
Clinical Trials Proj Spec I A
4 weeks ago
Rochester, United States University of Rochester Full timeOpening Full Time 40 hours Range URG 108 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project...
-
Clinical Trials Proj Spec I A
4 weeks ago
Rochester, United States University of Rochester Full timeGENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory...
-
Clinical Trials Proj Spec I A
3 weeks ago
Rochester, United States University of Rochester Full timeGENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory...
-
Clinical Trials Proj Spec I A
3 weeks ago
Rochester, United States University of Rochester Full timeOpening Full Time 40 hours Range URG 108 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project...
-
Human Subject Research Spec I
4 weeks ago
Rochester, United States University of Rochester Full timeOpening Full Time 40 hours Range URG 106 Ortho, Clinical Research Schedule 8 AM-4:30 PM; OCC WKNDS Responsibilities GENERAL PURPOSE: Coordinates the activities associated with human subject research. This person will be responsible for recruitment and have administrative responsibilities, including screening and recruiting subjects, performing informed...
-
Human Subject Research Spec I
3 weeks ago
Rochester, United States University of Rochester Full timeOpening Full Time 40 hours Range URG 106 Ortho, Clinical Research Schedule 8 AM-4:30 PM; OCC WKNDS Responsibilities GENERAL PURPOSE: Coordinates the activities associated with human subject research. This person will be responsible for recruitment and have administrative responsibilities, including screening and recruiting subjects, performing informed...