Director, Clinical Data Acquisition Strategy

Position Summary

The Director, Clinical Data Acquisition Strategy leads the delivery of strategy, technology roadmap, and processes for acquiring data for clinical trials, focusing on site and patient experience, providing data aligned with end-to-end data strategies, enabling analysis and reporting, and promoting automation.

• 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; 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; 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 their 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:
Bachelors required, advanced degree preferred.

Experience:

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

Track record:
Successful lead, influence, drive strategy and make decisions.

• 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 experience with leveraging automation and AI to enable processes.
• Demonstrated ability to deliver tangible impact by planning and executing strategic projects involving cross-functional stakeholders.
• Proven record of making decisions, resolving complex problems and driving significant initiatives to completion.
• Strong, clear oral and communication skills, including ability to craft communications and business cases for senior leadership.
• Strong knowledge of GCP/ICH guidelines.
• Demonstrated partnership across various collaborative and industry forums.
• Diverse and sufficient technical expertise to be a credible interface to all global development and business partners across clinical data acquisition types.
• Broad intelligence of clinical data acquisition including future trends.
• Influential leadership and communication skills.

Madison - Giralda - NJ - US: $200,980 - $243,544

Princeton - NJ - US: $200,980 - $243,544

Starting pay range(s) listed above for a full-time employee (FTE) basis; additional incentive cash and stock opportunities may be available.

• Health Coverage:
  Medical, pharmacy, dental and vision care.
• Wellbeing Support: BMS Well-Being Account, BMS Living Life Better, Employee Assistance Programs.
• Financial Well-being and Protection: 401(k), short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support and survivor support.
• Paid Time Off:
  Unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement and military needs, and an annual Global Shutdown between Christmas and New Years Day.

Bristol Myers Squibb is an equal opportunity employer and does…