Children's Hospital of Philadelphia

Data Coordinator - Profound Autism Research Study

Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in clinical informatics, sciences, math, statistics, healthcare management, or related field required
  • Master's Degree preferred
  • Experience with UKG (Ultimate Kronos Group) preferred
  • Experience using data to enhance healthcare quality preferred
  • Proficiency in Microsoft Access, Excel, and PowerPoint
  • Experience managing diverse, complex datasets
  • Strong communication skills to convey technical information clearly

Responsibilities

  • Monitor incoming study data for completeness and timeliness
  • Review data before submission to ensure accuracy and identify errors
  • Investigate quality flags and drive resolution of data issues
  • Track and follow up on open data issues to ensure timely corrections
  • Consult and train staff on data collection tools and best practices
  • Coordinate the transfer and upload of data to collaborators
  • Ensure compliance with SOPs and maintain accurate data records

Benefits

  • Comprehensive benefits package
  • Opportunities for professional development
  • Support for work-life balance
  • Engagement in cross-network collaboration and annual meetings
  • Access to a diverse range of data sources and technical partners
Full Job Description
SHIFT:
Day (United States of America)

A Brief Overview

Serves as the primary data liaison for a clinical research team conducting a Longitudinal Natural History Study (LNHS) in autism spectrum disorder. Monitors all study data streams to ensure submissions are complete, accurate, and on schedule; investigates and resolves data quality issues in collaboration with Research Assistants, Research Coordinators, and the Data Coordinating Center (DCC). Serves as the primary point of contact between the site team and external data partners including the DCC, Clinical Coordinating Center (CCC), study sponsor, and long-term data repository.

What you will do

Data Quality Monitoring and Issue Resolution
  • Monitors all incoming study data (clinical assessments, EHR, EEG, wearable/digital biomarker data, biospecimens) to confirm submissions are complete and on schedule.
  • Reviews data for completeness and accuracy before submission reaches the DCC; identifies and addresses errors early.
  • Receives and triages quality flags from the DCC; investigates root causes (data entry error, missed visit, equipment issue, protocol misunderstanding), determines who needs to be involved, and drives resolution to closure.
  • Tracks open data issues and follows up with staff to ensure flagged items are corrected and resubmitted in a timely manner.
  • Provides regular status reports to study leadership on data completeness, submission timelines, and outstanding issues.


Staff Training and Support
  • Consults with Research Assistants and Research Coordinators on correct use of data collection tools and Electronic Data Capture (EDC) systems such as REDCap.
  • Provides training and ongoing guidance on data collection SOPs, data organization, and open science best practices.
  • Identifies recurring error patterns and delivers targeted retraining to prevent downstream quality issues.
  • Promptly notifies study leadership of roadblocks that will impede data collection, submission, or analysis.


External Coordination and Data Submission
  • Serves as the primary point of contact between the site research team and external technical partners (DCC, CCC, study sponsor's data team, and long-term data repository) from project initiation through data release.
  • Coordinates upload and transfer of data to the DCC; manages communication during processing, harmonization, and quality control until datasets are finalized for release.
  • Tracks dataset status and submission readiness; communicates updates to external partners and consortium staff on a regular basis.
  • Collaborates with the CCC and DCC on metadata standards; ensures comprehensive metadata capture throughout the data lifecycle.


Documentation and Compliance
  • Ensures the site follows established SOPs, data dictionaries, metadata templates, and submission workflows set by the DCC; flags deviations and works with the Project Manager to bring the site back into compliance.
  • Maintains accurate, up-to-date records of data collection, submission, correction, and finalization status so that the state of any dataset is always known and reportable.
  • As needed, ensures site alignment with DCC-centralized analysis pipelines, computational models, and standardized processing tools.


Reporting and Network Engagement
  • Assists research staff in preparation and analysis of data for routine and special requests; supports the Project Manager and site leadership in preparing the annual Project Progress Report.
  • Participates in regularly scheduled Data Manager Community meetings and cross-site coordination calls with LNHS stakeholders and consortium Data Managers.
  • Optionally participates in international working groups and interest groups to support cross-network collaboration.
  • Attends annual in-person grantee meetings and other sponsor-mandated meetings.


Education Qualifications
  • Bachelor's Degree clinical informatics, sciences, math, statistics, healthcare management or other healthcare related degree Required
  • Master's Degree Preferred


Experience Qualifications
  • Experience with UKG (Ultimate Kronos Group formerly Kronos) Preferred
  • Experience using data to improve the quality of healthcare Preferred


Skills and Abilities
  • Proficient in Microsoft Access, Excel, and PowerPoint. (Required proficiency)
  • Experience working with datasets, combining data from a multitude of sources. (Required proficiency)
  • Ability to convey complex or technical information in a manner that others can easily understand. (Required proficiency)
  • Ability to manage multiple projects, work independently, take initiative and implement problem-solving capabilities. (Required proficiency)
  • Ability to work under stress and meet deadlines. (Required proficiency)
  • Strong ethical conduct and ability to work with confidential and highly sensitive information. (Required proficiency)
  • Good interpersonal skills; ability to work with clinical leaders in the use of data for improvement. (Required proficiency)


SALARY RANGE:

$83,700.00 - $106,700.00 Annually

Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.

At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP's Compensation and Benefits.

About Children's Hospital of Philadelphia

The Children's Hospital of Philadelphia (CHOP) is a pediatric healthcare facility that provides a range of medical services to children and families. The hospital was founded in 1855 and is located in Philadelphia, Pennsylvania. CHOP has a team of over 16,000 employees, including doctors, nurses, and other healthcare professionals. The hospital offers services such as primary care, specialty care, and surgical services. CHOP is consistently ranked as one of the top children's hospitals in the US by U.S. News & World Report.
Learn more about Children's Hospital of Philadelphia
Size
16,000 employees
Industry
Founded
1855

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