Abbott Clinical Data Specialist in St. Paul, Minnesota

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.


The Clinical Database Specialist (CDS) is responsible for performing data management tasks, including clinical study database design. The CDS is capable of supporting clinical trials from initial data collection to database lock and closure with general mentoring and coaching from data management peers and management.


Represents Data Management on Clinical Project Teams through the following:

  • Attend Clinical Project Team meetings to gather business need requirements and translate to technical requirements

  • Partner with other shared service functions such as Safety, Core Lab, etc. to gather business need requirements and translate to technical requirements

  • Train database End Users (internal and external users) on the database and/or maintain automated database training system

  • Capture and maintain Database and Systems training records

  • Assists in FDA and Quality audits that involve Clinical Database and Data Management

  • Lead development and quality control (QC) of data management documents including data management plans, data review guidelines, and database validation protocols

  • Follows and implements data management standards and best practices and assures Standard Operating Procedures are followed for Data Management activities

Contributes to the development and maintenance of Clinical Database systems, including EDC, Edit Checks, Reporting, Study Notifications, Security, etc. through the following:

  • Partners with Clinical Team to translate Site Contracts to programmatic payment rules

  • Understands clinical trial payment systems and process

  • Partner closely with DM Management, Database Developers/Analysts, and Programmers to drive database and system deliverables

  • Translate business requirements into technical requirements for eCRFs, edit checks, study notifications and customizations in the study database

  • Perform and document functional and/or user acceptance testing on study databases, reports, study notifications, and database customizations

  • Ensure that appropriate data validation (edit check) specifications and quality control checks are implemented per study needs

  • Effectively communicate with the Clinical Project Team and other key stakeholders regarding the deliverable, including timeline, workaround, etc.

  • Process database accounts and reviews accounts regularly to ensure integrity of database access and security

Lead data cleaning and data freeze/lock efforts for regulatory submissions and other business needs as requested by the Clinical Project Team through the following:

  • Lead data review meetings with the Clinical Project Team and Statistics to identify data cleaning issues and strategize cleaning efforts

  • Project plan interim and final database lock and data reviews; monitor overall data management tasks to ensure that timelines are met and that any issues are proactively identified and resolved

  • Coordinate and ensure completion of all aspects of data review, including running validation procedures, issuing queries, database QC, SAE Reconciliation, medical coding, and database closure activities per work instructions and SOPs as applicable

  • Design tools and reports to document data review and assist in data cleaning activities

  • Lead and document data freeze activities with the Clinical Project team, Biostatistics, and SAS programmer

  • Utilize existing tools and database to identify data issues and drive resolutions with the Clinical Project Team in a timely manner

Perform other duties as assigned.


** General knowledge of clinical study lifecycle from protocol design to database development and study closure.

** Proficiency with using EDC databases, preferably Clindex.

** Experience working under Good Clinical Practices, Good Clinical Data Management Practices, and other FDA regulations and guidelines is required.

** Demonstrated solid oral and written communication skills and analytical/problem-solving skills are essential as is the ability to clearly communicate basic data management concepts to those outside data management.

** Must be able to effectively manage multiple projects and timelines.

** Must be able to travel up to 5% per year.

** Requires the ability to sit or stand while working on a computer for an extended period.


Bachelor’s degree (REQUIRED) in computer sciences or a scientific discipline with a minimum of 2+ years of experience in a medical device clinical research or data management position is required.


An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email