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Director, Clinical Data Acquisition Strategy

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: Bristol Myers Squibb
Full Time position
Listed on 2026-06-06
Job specializations:
  • IT/Tech
    Data Analyst, Data Engineer, Data Science Manager
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Working with Us

Challenging. Meaningful. Life‑changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible.

Functional Area

Description

GDM is responsible for clinical trial data acquisition, data management, and data review, ensuring quality data for trials across the BMS R&D portfolio.

Position Summary

The Director, CDA Strategy is a leadership role with responsibility for delivering the strategy, technology roadmap, and processes for acquiring data for our clinical trials, keeping the site and patient experience at the forefront, providing data in line with end-to-end data strategies, enabling analysis and reporting and promoting automation. This role reports to the Head of Clinical Data Acquisition within GDM and is a full‑time, office‑based position.

Position

Responsibilities
  • Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data strategies. Developing the technology roadmaps required to deliver the strategy, promote automation and embed AI.
  • Defining the processes, technologies and data flows required to collect new data types and deliver data to end users and/or to make significant updates to existing data types, ensuring standardization and integration across end-to-end data flow.
  • Developing key data collection components designed to optimize the site and patient experience while ensuring downstream data requirements for analysis and reporting are effectively met.
  • Leading broad cross‑functional initiatives to establish industry‑leading data capture capabilities, e.g., EMR to EDC to source data directly from EMRs. This includes creating project charters, project plans, sponsorship communications, implementation plans and driving projects from start to finish.
  • Developing senior leadership level communications to share strategies, make proposals, and update on strategic initiatives. This could include business cases.
  • Making decisions, solving complex problems and delivering on accountabilities.
  • Staying on top of industry evolution to simplify/enhance user experience, leverage automation/AI, deliver operational efficiencies, and make appropriate investments to stay ahead of technology/data trends.
  • Leading the development and maintenance of procedural documents which are reflective of industry standards and regulatory requirements and include optimal processes.
  • Developing strong and productive working relationships with key leaders throughout GDM, DQS, Drug Development and BMS with the ability to think strategically and effectively express his/her views to senior management.
  • Developing strong and productive working relationships with key vendors in the clinical data acquisition space and proposing the right advancements with the right vendors.
  • Representing BMS in interactions with key external partners as part of any committee or industry group relating to data collection.
Degree / Experience Requirement

Bachelors degree required with an advanced degree preferred.

At least 10 years of relevant strategy, technology and process experience specifically within clinical data acquisition across modalities (ie, site‑collected, external, eCOA and device/digital data) including data integration, automation and incorporation of AI.

Successful track record of leading, influencing, driving strategy and making decisions.

Key Competency Requirements
  • Expert understanding of clinical data acquisition strategy, processes, technologies and end to end data flows.
  • Proven expertise in EDC (including Medidata Rave), external vendor data, eCOA, and digital/device data, including strategy, processes and tools.
  • Demonstrated…
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