Bristol Myers Squibb
SeniorManager,ClinicalDataReportingandAnalytics
Neural analysis suggests this role is
optimal for Senior candidates.
“Senior Manager, Clinical Data Reporting and Analytics at Bristol Myers Squibb. Skills: Clinical Data Reporting, Analytics, Stakeholder Collaboration, Report Development, Data Analysis. Serve as the primary point of contact for multiple studies in different Therapeutic Areas.. Collaborate with clinical stakeholders to understand their reporting and analytics needs aligned with study protocols.”
What You'll Achieve.
ensuring a "first time right" approach; ensure patient safety; efficient report delivery; support business priorities
Industry & Context.
translate requirements into comprehensive reporting development specifications; suggest solutions; develop solutions for complex reporting needs
Flexible to work with global stakeholders across different time zones while ensuring business continuity.
What They're Looking For.
Must Have
Experience with reporting tools, Experience with analytics visualizations, Experience with documentation and process compliance, Experience with clinical trial needs analysis, Experience with reporting development specifications, Experience with testing developed reports, Experience with peer review support, Experience with procedures, trainings, and policies defined by the organization
Nice to Have
Keeping up to date with new reporting tools, techniques, and industry trends
What You'll Do.
Serve as the primary point of contact for multiple studies in different Therapeutic Areas.
Collaborate with clinical stakeholders to understand their reporting and analytics needs aligned with study protocols.
Translate requirements into comprehensive reporting development specifications.
Utilize standard reports whenever possible and to suggest solutions.
Develop reports and analytics visualizations according to specified requirements
ensuring a "first time right" approach.
Test developed reports
and provide peer review support as needed.
Adhere to documentation and process compliance
notifying management of any noncompliance.
Analyse clinical trial needs holistically to determine effective monitoring approaches and ensure patient safety.
Negotiate with stakeholders and foster collaboration for efficient report delivery.
Prioritize deliverables based on business criticality and seek assistance when needed.
Demonstrate technical expertise to develop solutions for complex reporting needs.
Work cohesively with team members
embracing feedback and suggestions.
Keeping up to date with new reporting tools
and industry trends to enhance skills and knowledge.
Ensure compliance with procedures
and policies defined by the organization.
Contribute to other sub-functions of CDR&A as needed to support business priorities.
Flexible to work with global stakeholders across different time zones while ensuring business continuity.
How You'll Work.
Team & Collaboration
Collaborate with clinical stakeholders; Work cohesively with team members; foster collaboration for efficient report delivery
Communication Scope
Negotiate with stakeholders
Process & Methodology
Prioritize deliverables based on business criticality
Full Job Description
**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. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). 1\. Serve as the primary point of contact for multiple studies in different Therapeutic Areas. 2\. Collaborate with clinical stakeholders to understand their reporting and analytics needs aligned with study protocols. 3\. Translate requirements into comprehensive reporting development specifications. 4\. Utilize standard reports whenever possible and to suggest solutions. 5\. Develop reports and analytics visualizations according to specified requirements, ensuring a "first time right" approach. 6\. Test developed reports, document results, and provide peer review support as needed. 7\. Adhere to documentation and process compliance, notifying management of any noncompliance. 8\. Analyse clinical trial needs holistically to determine effective monitoring approaches and ensure patient safety. 9\. Negotiate with stakeholders and foster collaboration for efficient report delivery. 10\. Prioritize deliverables based on business criticality and seek assistance when needed. 11\. Demonstrate technical expertise to develop solution
Applying for this Senior Manager, Clinical Data Reporting and Analytics role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Bristol Myers Squibb?
Real rants from real employees. Read before you apply.