Exelixis

Statistical Programming Manager

Exelixis$139K — $198K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Minimum of 5-7 years of statistical programming experience in clinical data, preferably in the Biotech/Pharmaceutical industry.
  • Proficient in SAS programming (SAS/Base, SAS/Stat, SAS Macros); experience with UNIX, R, and Tableau is desirable.
  • Bachelor's degree in a related field (BS/BA) required; advanced degrees (MS/MA or PhD) or equivalent experience preferred.
  • Strong ability to communicate effectively, both verbally and in writing, in a timely manner.
  • Experience adhering to FDA regulations and understanding of CDISC standards required.

Responsibilities

  • Independently develop SAS programs and specifications for study analyses, including Integrated Safety Summaries.
  • Lead or support programming efforts, coordinating tasks with clinical data management and biostatistics teams.
  • Oversee dataset development in SDTM format by CROs, ensuring compliance with documentation standards.
  • Program quality control checks for CRO deliverables, including datasets and reporting outputs.
  • Independently verify results from other programmers and troubleshoot project issues.
  • Manage multiple tasks effectively, prioritizing based on business needs and timelines.
  • Communicate with cross-departmental teams to facilitate data integration and project deliverables.

Benefits

  • 401k plan with generous company contributions
  • Comprehensive group medical, dental, and vision coverage
  • Life and disability insurance offerings
  • Flexible spending accounts available for employees
  • Eligibility for a discretionary annual bonus program
  • Opportunity to purchase company stock and receive long-term incentives
  • Generous paid time off: 15 vacation days, 17 paid holidays, and up to 10 sick days per year.
Full Job Description
SUMMARY/JOB PURPOSE:

Performs statistical analysis on data related to product development in a research and development environment. Uses statistical software (SAS, R, etc) and/or data visualization tools (Tableau) to create and maintain listings, tabulations, graphical summaries, and formal statistical estimates and tests. Creates datasets in a standard format (i.e. SDTM), analysis datasets (i.e. ADAM), assesses quality of data analysis programs, and develops automated analysis tools, where appropriate. Develops programs to assist with data review such as edit checks and custom listings. May be responsible for data integration used for clinical summaries and/or creation and quality control of statistical submission components to regulatory agencies. May partner with biostatisticians and clinical data management staff in establishing standards for clinical data collection, management and/or reporting of data.

Essential Duties And Responsibilities:
• Independently develops SAS or other programs, and specifications (e.g. SDTM, ADaM), for use in study or other analyses, such as Integrated Safety Summaries.
• May serve as a lead or support programmer
• If the lead programmer on studies, works with clinical data management staff and biostatisticians to coordinate and schedule data transfers and the delivery of required outputs. Responsible for helping to identify when additional programming resources are needed for a project, communicating with their supervisor to arrange for those resources, and coordinating and overseeing other statistical programmers' work on the project as needed.
• Oversees the development of datasets in SDTM format by CROs, including clear documentation of the process that was followed in the form of specifications, trackers, and checklists.
• Responsible for programming QC oversight of CRO deliverables such as analysis datasets and tables, listings, and figures (TLFs).
• Independently verifies other programmer's results.
• Adheres to FDA regulations regarding training records, guidelines, and SOPs.
• Adheres to company SOPs and department guidelines.
• Produces study datasets and programs that meet CDISC standards and regulatory requirements.
• Supports Ad-hoc requests as needed.
• Works on multiple tasks at the same time and prioritize tasks to meet business needs.
• Trouble-shoots technical and project issues.
• Communicates with outside departments and/or groups.

Supervisory Responsibilities:
• None

EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education/Experience:
• BS/BA degree in related discipline and a minimum of seven years of related experience; or,
• MS/MA degree in related discipline and a minimum of five years of related experience; or,
• PhD in related discipline and 0 or more years of related experience; or,
• Equivalent combination of education and experience.
• May require certification in assigned area.

Experience/The Ideal for Successful Entry into Job:
• Typically requires at least seven years experience in statistical programming with clinical data and SAS.
• Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros.
• UNIX, S-Plus, R, Tableau, CDISC, and SAS/GRAPH experience desirable.
• Ability to communicate verbally and in writing in a clear and timely manner.
• Experience in Biotech/Pharmaceutical industry preferred.

Knowledge/Skills:
• Has extensive experience in relevant industry/profession and area of specialization.
• Uses professional concepts and company objectives to resolve complex issues in creative and effective ways.
• Identifies and implements methods and procedures to achieve results.
• Leads or manages the work of others by providing guidance to subordinates or teams based on organizational goals and company policy, with responsibility for results, including costs, methods and staffing.
• Must be able to program defensively, check results, and consistently produce accurate output.
• Performs a variety of complicated tasks with a wide degree of creativity and latitude.
• Has complete understanding and wide application of technical principles, theories, concepts and techniques.
• Has good general knowledge of other related disciplines.
• Applies strong analytical and business communication skills.
• Meets timelines on a regular basis.

JOB COMPLEXITY:
• Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors.
• Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation of criteria for obtaining results.
• Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
• Networks with key contacts outside own area of expertise.

#LI-JP1

Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $139,500 - $198,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.

In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

About Exelixis

Exelixis is a biotechnology company that develops and commercializes innovative medicines for the treatment of cancer. The company's flagship product, CABOMETYX® (cabozantinib), is an inhibitor of multiple tyrosine kinases, including MET, AXL, and VEGFR, which are involved in the growth and spread of cancer cells. CABOMETYX is approved in the United States for the treatment of advanced renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC), and is also approved in the European Union and other countries for the treatment of advanced RCC. Exelixis is headquartered in Alameda, California, and has additional offices in South San Francisco, California, and Basel, Switzerland. Learn more at www.exelixis.com.
Learn more about Exelixis
Size
954 employees
Market Cap
$5 billion
Industry
Net Income
$111.7 million
5 Year Trend
+49.6%
Revenue
$987.5 million
NASDAQ

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