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Director of Clinical Trial Analytics

Employer
Bristol Myers Squibb Company
Location
Princeton, NJ, United States
Start date
Oct 17, 2019

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Discipline
Clinical, Clinical Trials
Required Education
Masters Degree/MBA
Position Type
Full time
Hotbed
Pharm Country, Best Places to Work

Job Details

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Job Description - Scientific and Analytic Expertise Required
  • Leads a team of Associate Directors and Senior Specialists who are in charge of clinical trial design and operational pressure testing, enrollment/randomization planning, scenario modeling, performance forecasting and tracking for Phase I to IV clinical trials across all therapeutic areas
  • Provides strategic leadership for the establishment and ongoing analytic support of a new business model in clinical operations for the entire Oncology portfolio
  • Explores the needs of and develops and implements a custom analytic support model for multi-cohort multi-tumor, escalation and expansion phase Early Oncology pipeline
  • Represents the group in industry level or company-wide initiatives to develop, implement and maintain cutting edge digital solutions to increase our portfolio speed (including, but not limited to Transcelerate, Digital Helath, PPM and others)
  • Provides oversight for the analytic aspects of the late stages of drug development at a variety of internal forums, increase understanding of metrics and forecasts, particularly with respect to timeline analytics and uncertainty
  • Responsible for resource utilization and demand management in the Metrics and Reporting group
  • Manages the team through the company transformation and ensures that business requirements are always met in a changing and evolving environment
  • Represents the Clinical Trial Analytics perspective across GCO and beyond
  • Deeply understands the utility of RWD in clinical trial planning, drives the creation of solutions in study design, trial pacement, patient selection
  • Interacts with R&D leaders, GCO leadership, Operations Leads, Protocol Managers, Site Managers and other stakeholders as appropriate
  • Provides strategic direction and oversees the creation of recruitment dashboards, enrollment projections, Eclipse reports, and ad hoc custom outputs
  • Manages vendor relationships, creates strategy for long term engagement and identifies solutions for short term deliverables
  • Dynamically leverages the existing contractor pool to maximize performance and manage workload peaks.
  • Fully responsible for the assigned team's development, coaches and mentors them according to their needs
  • Accountable for driving continuous improvement and innovation in the Feasibility and also the Forecasting team and at the CT Analytics level. Identifies areas for improvement and acts as a sponsor or contributor to work streams and other CI initiatives.


Qualifications

Requirements:
  • Masters degree in public health, epidemiology, health care or other life-sciences.
  • 7+ years experience in clinical trial management or clinical trial information support.
  • Strong understanding of clinical trial processes.
  • Excellent analytic skills
  • Strong understanding of Immune-Oncology
  • Experience with portfolio planning, trial design, country and site selection, trial feasibility, performance tracking and vendor management.


Skills:
  • Strong people management and inter-personal skills.
  • Excellent presentation of insights
  • Customer focus
  • Attention to detail
  • Experienced with information systems and clinical trial intelligence and supporting data
  • Extremely proficient with MS Office (Word, Excel, ppt). VBA, ORACLE, SAS or R is a plus
  • Ability to handle multiple projects
  • Strong analytical competencies
  • Exposure to, and understanding of epidemiological, healthcare, commercial and clinical data sets as it relates to clinical trial planning and execution
  • Strong understanding of the digital evolution in clinical research
  • Understanding of non-clinical Real World Data (EMR, Claims, ...)
  • Strategic thinking


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 the resources to pursue their goals, both at work and in their personal lives.

Company

Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

At Bristol Myers Squibb, we believe in the power of science to address some of the most challenging diseases of our time. Our focus on these unmet needs comes during a remarkable time, when unprecedented scientific breakthroughs are advancing the treatment of disease as never before in human history.

We work every day to transform patients’ lives through science. Each day, our employees around the world work together for patients – they are at the center of everything we do. They inspire us. They are the reason we come to work each day.

We combine the agility of a biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation.

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Company info
Website
Phone
+1-800-332-2056
Location
430 E. 29th St
14th Floor
New York
New York
10016
United States

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