We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Data Core Manager / Hybrid - 137621

UC San Diego
United States, California, San Diego
Dec 04, 2025

La Jolla

9500 Gilman Drive, San Diego, CA 92093, United States
#137621 Data Core Manager / Hybrid Filing Deadline: Thu 12/18/2025
Apply Now
UC San Diego values and welcomes people from all backgrounds. If you are interested in being part of our team, possess the needed licensure and certifications, and feel that you have most of the qualifications and/or transferable skills for a job opening, we strongly encourage you to apply.

UCSD Layoff from Career Appointment: Apply by 12/08/25 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor.

Reassignment Applicants: Eligible Reassignment clients should contact their Disability Counselor for assistance.

This position will work a hybrid schedule which includes a combination of working both onsite in La Jolla, CA and remote.

DESCRIPTION

Applies skills as a seasoned, experienced data / information management professional with full understanding of industry practices and campus / medical center / OP and department methodologies, policies and procedures to resolve complex and wide ranging issues where analyses of situations or data requires a review of a variety of factors. Demonstrates competency in selecting methods and techniques to obtain solutions. Applies professional and broadly defined research analysis and data / information administration and data use concepts to manage and perform complex assignments. Build and maintain research databases including eCRFs, visit schedule development, edit check programming and modifications. Support eCRF library development using accepted standards. Liaison with SDSC to build system to meet user requirements.

Independently analyzes complex information requirements and documents them using formal data definition techniques and naming standards. Gathers, analyzes, prepares and summarizes information from subject matter experts and technical personnel. Researches relevant problem domain literature and information standards and develops recommendations for data management resource plans including approaches, trends, sources and uses. Schedule and lead eCRF design and review meetings. Import/load external data into clinical database and perform reconciliation.

Independently designs information transformation processes. Designs and implements capture of metadata from technical processes such as software design and database management. Performs complex data management or resource research and studies for a variety of constituents and plans metadata acquisition for sets of unstructured data objects such as collections of images or documents. Designs systems architecture, assess and implements reorganization and optimization plans, manages and oversees administration of systems. Creates standard format and naming conventions for data files and data structures. Oversee the data warehouse used to managelibraries of study data including image, source document and data files. Recognizes and highlights potential issues with current systems and processes and suggests potential improvements.

MINIMUM QUALIFICATIONS
  • Seven years of related experience, education/training, OR a Bachelor's degree in related area plus three years of related experience/training.

  • Ability to prepare data models unassisted.

  • Familiarity with data model patterns in one or more common business or academic domains.

  • Familiarity with logical data design and data mapping or data conversion.

  • Familiarity with data quality and governance issues and requirements.

  • Ability to represent relevant information in abstract models.

  • Thorough knowledge of data management systems, practices and standards.

  • Thorough knowledge of relevant rules and regulations. Such as HIPAA compliance.

  • Demonstrated ability to work with others from diverse backgrounds. Demonstrated effective communication and interpersonal skills. Demonstrated service orientation skills.

  • Demonstrated ability to communicate technical information to technical and non-technical personnel at various levels in the organization.

  • Self-motivated and works independently and as part of a team.

  • Demonstrated strong problem-solving skills. Able to learn effectively and meet deadlines.

  • Strong organizational skills.

  • Strong analytical and design skills, including the ability to abstract information requirements from real-world processes to understand information flows in computer systems.

  • Ability to represent relevant information in abstract models. Critical thinking skills and attention to detail.

  • Experience working with data and systems pertaining to research trials and the special considerations for data integrity trials is required.

  • A minimum of 3-5 years of study base build working experience in a medical research setting.

  • Experience working with data and systems pertaining to research trials and the special considerations for data integrity trials.

  • Experience managing large, multi-site longitudinal data sets.

  • Strong technical mastery (databases, coding, integration), regulatory and compliance expertise, data governance skills, and domain knowledge in ADRD research. Ability to bridge the gap between raw data collection and scientific analysis, ensuring data are high-quality, harmonized, and compliant with standard requirements.

  • Experience with SQL (MySQL, PostgreSQL, Oracle, or MS SQL Server); Research Data Systems such as REDCap, LIMS (Laboratory Information Management Systems), XNAT (imaging), and specialized ADRC/NACC platforms; Programming / Scripting with proficiency in Python, R, or SAS for data cleaning, validation, and analysis pipelines; Data Integration: with experience managing multi-modal data (clinical, cognitive assessments, imaging, neuropathology, genetics, biospecimen tracking).

PREFERRED QUALIFICATIONS
  • Data Standards and Regulatory Compliance: NACC UDS familiarity (Uniform Data Set forms and longitudinal data standards required by ADRCs); NIH / NIA data sharing policies (e.g., uploading to NACC, GAAIN, AD Knowledge Portal); HIPAA compliance and PHI handling; Good Clinical Data Management Practices (GCDMP); Understanding of data dictionaries, metadata standards (CDISC, HL7, OMOP).

  • Familiarity with clinical trial data, cognitive assessments (MMSE, MoCA, CDR, etc.), neuroimaging (MRI, PET), and neuropathology staging (Braak, Thal, CERAD); Understanding of longitudinal research challenges (attrition, missing data, variable follow-up schedules); Awareness of emerging biomarkers (fluid biomarkers, genetics, digital assessments).

SPECIAL CONDITIONS
  • Employment is subject to a criminal background check.

Pay Transparency Act

Annual Full Pay Range: $88,000 - $161,600 (will be prorated if the appointment percentage is less than 100%)

Hourly Equivalent: $42.15 - $77.39

Factors in determining the appropriate compensation for a role include experience, skills, knowledge, abilities, education, licensure and certifications, and other business and organizational needs. The Hiring Pay Scale referenced in the job posting is the budgeted salary or hourly range that the University reasonably expects to pay for this position. The Annual Full Pay Range may be broader than what the University anticipates to pay for this position, based on internal equity, budget, and collective bargaining agreements (when applicable).

Apply Now

If employed by the University of California, you will be required to comply with our Policy on Vaccination Programs, which may be amended or revised from time to time. Federal, state, or local public health directives may impose additional requirements.

If applicable, life-support certifications (BLS, NRP, ACLS, etc.) must include hands-on practice and in-person skills assessment; online-only certification is not acceptable.

UC San Diego Health Sciences is comprised of our School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, The Herbert Wertheim School of Public Health and Human Longevity Science, and our Student Health and Well-Being Department. We have long been at the forefront of translational - or "bench-to-bedside" - research, transforming patient care through discovery and innovation leading to new drugs and technologies. Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care. We invite you to join our team!

Applications/Resumes are accepted for current job openings only. For full consideration on any job, applications must be received prior to the initial closing date. If a job has an extended deadline, applications/resumes will be considered during the extension period; however, a job may be filled before the extended date is reached.

To foster the best possible working and learning environment, UC San Diego strives to cultivate a rich and diverse environment, inclusive and supportive of all students, faculty, staff and visitors. For more information, please visit UC San Diego Principles of Community.

The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.

For the University of California's Anti-Discrimination Policy, please visit: https://policy.ucop.edu/doc/1001004/Anti-Discrimination

UC San Diego is a smoke and tobacco free environment. Please visit smokefree.ucsd.edu for more information.

UC San Diego Health maintains a marijuana and drug free environment. Employees may be subject to drug screening.



Apply
Applied = 0

(web-df9ddb7dc-vp9p8)