Senior Preclinical Data Engineer

ALTEN

$90K — $140K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5-6 years of direct experience with preclinical research data
  • Willingness to be on-site a minimum of 3 days per week in Boston, MA
  • Strong bench science understanding and familiarity with scientific data outputs
  • Experience establishing data standards from scratch
  • Proficiency in SQL and basic Python for data handling
  • Ability to provide end-user support for scientific data systems
  • Independent work capability under remote management.

Responsibilities

  • Act as the main contact for preclinical data management activities
  • Collect and transform diverse preclinical data into standardized formats
  • Develop and implement new data standards and taxonomies
  • Conduct data quality checks and validations using SQL and Python
  • Load validated data into a central data lake
  • Provide user support for scientific research tools
  • Resolve issues related to data handling across systems
  • Facilitate functional administration tasks, including access management and documentation
  • Assist in application testing and validation
  • Support the creation of BI dashboards and reports.

Benefits

  • Remote working structure with flexible hours
  • Opportunity to work at the forefront of preclinical research
  • Collaboration with global teams and experts
  • Access to professional development resources
  • Involvement in setting data standards and processes.
Full Job Description
We are seeking a Senior Preclinical Data Engineer to support preclinical research and development activities across multiple global sites. This is a hands-on data role focused on managing, standardizing, and supporting highly heterogeneous preclinical bench and laboratory data from multiple internal systems. The successful candidate will operate independently within a remote team structure, helping to establish data standards, ensure data quality, support end users, and contribute to central data management initiatives.

Responsibilities:

  • Serve as the on-site point of contact for preclinical data management activities while operating under the direction of a remote platform team.
  • Collect, map, and transform heterogeneous preclinical data, including in vitro and in vivo bench/lab-generated data, from multiple internal systems into standardized and usable formats.
  • Support the development and implementation of data standards and taxonomies where no existing standards currently exist.
  • Perform data quality reviews, data cleaning, validation, and accuracy checks using SQL and Python.
  • Contribute to the loading of validated and standardized data into a central data lake.
  • Provide functional, ticket-based user support for scientists using internal preclinical research tools.
  • Troubleshoot data-loading and data-handling issues across multiple preclinical systems.
  • Support functional administration activities, including:
    • Access rights management
    • List-of-values (LOV) management
    • Functional documentation, such as methods of procedure (MOPs)
    • Business needs refinement
  • Support application testing and validation activities, including:
    • Test case development
    • Test execution
    • Validation documentation
  • Set up or support business intelligence (BI) extracts, dashboards, and reports.


Qualifications:

  • Minimum of 5 to 6 years of experience working directly with preclinical or bench/lab-generated research data.
  • Ability to work a minimum of 3 days on-site in Boston, MA.
  • Strong understanding of bench science and how scientific experiments generate data, including familiarity with outputs from techniques such as chromatography and Western blotting.
  • Demonstrated experience working with data that lacks established standards or formats, with the ability to create structure and standards from the ground up.
  • Working proficiency in SQL and basic Python for data querying, cleaning, validation, and quality review.
  • Experience providing end-user support and troubleshooting for scientific software applications or data systems.
  • Ability to work independently with remote management and limited local technical support.
  • Fluent in written and spoken English.

Preferred Qualifications:
  • Exposure to preclinical research domains such as pharmacology, toxicology, DMPK, or omics.
  • Familiarity with LIMS, ELN, or SDMS platforms.
  • Knowledge of data governance concepts, including Master Data Management (MDM), FAIR principles, and ALCOA+ data integrity practices.
  • Experience working as an embedded consultant or vendor within a client team.


Salary Range: $90,000 - $140,000

The actual salary offered is dependent on various factors including, but not limited to, location, the candidate's combination of job-related knowledge, qualifications, skills, education, training, and experience.

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