Senior Biostatistical Programming Director

Bristol-Myers Squibb

San Diego (CA)

On-site

USD 227,418 - 275,577

Full time

14 days+
Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Benefits offered by this job

Health Coverage
Wellbeing Support
401(k) plan

Job summary

Bristol-Myers Squibb is seeking a Director of Biostatistical Programming in San Diego to lead the development of clinical study deliverables. This role involves overseeing study vendor programming and collaborating with cross-functional teams.

The ideal candidate should have 15+ years in the pharmaceutical industry, a strong background in SAS programming, and experience in oncology. Additional benefits include flexible time off and wellness programs.

Qualifications

  • At least 15 years’ experience in pharmaceutical industry.
  • Experience managing CRO relationships.
  • In-depth knowledge of FDA regulations.

Responsibilities

  • Oversee vendors' activities and review deliverables.
  • Participate in analyzing and reporting clinical trial data.
  • Collaborate with cross-functional teams on study documents.

Skills

SAS programming
Statistical reporting
CDISC standards
Oncology experience

Education

Bachelor's degree in statistics or mathematics
Master's degree in statistics or computer science

Tools

SAS
CDISC

Job description

Bristol-Myers Squibb is seeking a Director of Biostatistical Programming in San Diego to lead the development of clinical study deliverables. This role involves overseeing study vendor programming and collaborating with cross-functional teams.

The ideal candidate should have 15+ years in the pharmaceutical industry, a strong background in SAS programming, and experience in oncology. Additional benefits include flexible time off and wellness programs.

Get your free, confidential resume review.

or drag and drop your file here.