Sr. Manager, Clinical Trial Analytics

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 rich in diversity. 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.

The Senior Manager, Global Feasibility is an experienced clinical research professional who has a strong proficiency in the curation and analysis of clinical trial intelligence data and its application to effectively conduct study feasibility assessments, country/site selection activities and the creation/maintenance of data-driven patient recruitment and enrollment forecasts for clinical trial(s) within a clinical research development program.   

Key demonstrated skill level for a Senior Manager, Global Feasibility are as follows: 

• Ability to set priorities and manage multiple projects within minimal oversight  

• Aware of and contributes to mitigation planning associated with industry trends, best practices and/or potential risks that may impact the development strategy of an asset, disease or clinical study.  

• Recognizes and identifies problems and recommends solutions. 

• Ability to articulate data insights to study team members and influence decision making 

• Ability to quickly assimilate new skills and integrate core procedures as well as to provide functional input into updating/enhancing procedures. 

• Easily builds cross functional relationships 

Key Responsibilities and Major Duties 

• Provide input into the clinical development strategy for an indication or program 

• Provides input into indication and/ or across asset planning (e.g. country/ site tiering) 

• Provides requested data analytics/insights to support business development evaluations. 

• Responsible for the conduct of a study feasibility assessment for phase I- III clinical studies. 

• Collection and analysis of internal and external competitive intelligence data (e.g. incidence/prevalence of a disease, drug landscape, clinical trial landscape, treatment regimen) and its influence on protocol design, patient recruitment potential and study execution. 

• Leads activities pertaining to country and site identification, feasibility and selection within a clinical study. 

• Collection and analysis of internal and external data (e.g. local treatment standard of care, available treatment options approved/reimbursed, local incidence/prevalence of disease, access to targeted patient population) and define an optimal geographic country footprint and proposed sites for participation in a cl