AbbVie Senior Manager, Early Oncology Statistics in Redwood City, California
Senior Manager, Early Oncology Statistics
USA, California, Redwood City
2 additional locations
USA, Illinois, Lake CountyUSA, California, South San Francisco
Research & Development
Oncology is a key therapeutic area for AbbVie, with a portfolio consisting of three marketed products — Imbruvica, Venclexta, and Empliciti — and a pipeline containing multiple promising new molecules that are being studied in nearly 200 clinical trials in 19 different types of cancer.
AbbVie is expanding its oncology hub on the West Coast, with three sites in the San Francisco Bay Area (Redwood City, South San Francisco, and Sunnyvale) focused on the discovery and development of novel oncology therapies. More than 1,000 AbbVie scientists, clinicians, and product developers with strong entrepreneurial roots work across these three sites. They combine their expertise in immuno-oncology, stem cells, and cell-signaling with their knowledge of bispecific antibodies, antibody-drug conjugates (ADCs), and covalent-inhibitor technologies to discover and develop novel cancer treatments. There is flexibility for this position to be based at our South San Francisco (CA), Redwood City (CA), or Lake County (IL) location.
- Provides scientific and statistical expertise for drug discovery or development strategies for assigned project in early-stage oncology; for the design, analysis, and reporting of scientific research trials; and for interacting with regulatory agencies regarding the results of these activities.
Directs the development of scientific protocols, ensuring they are scientifically sound and make optimal use of the data to be collected
Ensures research hypotheses and corresponding study designs are aligned with the project strategy, and meet scientific and/or regulatory needs
Ensures statistical methodology is appropriate and sound, consistent with the objective(s) of the scientific protocol
In collaboration with Data Sciences, Statistical Programming and other stakeholders, ensures data collection instruments are designed to capture protocol-specified scientific information and study databases (e.g., SAS, MS Access, Excel) are implemented such that short- and long-term project needs can be achieved
Oversees or partners in development of data quality assurance checks, ensuring accuracy and consistency of data released for statistical analysis
Demonstrates extensive understanding of statistical concepts and methodologies
Proposes new/novel statistical methodological approaches leading to improvements in the efficiency and sensitivity of study results
Provides sufficient detail to allow programming implementation
Ensures that all the statistical analyses specified in scientific protocols and/or analysis plans are conducted appropriately
Scientific Reports and Publications:
Ensures that study results and conclusions are scientifically sound, clearly presented, and supported by the statistical analyses provided
Prepares oral and written reports to effectively communicate results of clinical/scientific research to AbbVie management, project teams, regulatory agencies, or individual investigators
Provides in-depth scientific/statistical review for scientific reports and publications
Consultation: Works collaboratively with members of multi-function teams to complete project deliverables per agreed timelines. Keeps management informed on important scientific/statistical issues that may arise, in a timely manner. In collaboration with Statistical Programming or their designee, ensures that all programs meet analysis requirements, internal standard operating procedures, validation, and external regulatory requirements. Communicates with statisticians outside AbbVie concerning technical issues, building external scientific contacts, fostering professional development, and promoting the reputation of the department. Effectively and persuasively presents statistical concepts, evidence, assessment of risks and impacts, and logical arguments to management, regulatory agencies, and scientists. Demonstrates an understanding of drug development principles for assigned projects.
Project Team Involvement: Represents Data and Statistical Sciences (DSS) or Biometrics on assigned project team(s) to provide functional area input to compound/drug development. Serves as a liaison between the project team and DSS or Biometrics to ensure timely communication of project team updates, proper statistical strategies, and alignment of priorities between the project team and functional area.
Training, Supervising, Mentoring: Mentors junior staff and other development stakeholders with regards to statistical methodology and departmental operations
Participates in department seminars, short courses, and the publication presentation of scientific articles
Participates in departmental activities including recruiting, training/mentoring, research efforts, and cross-functional collaborations, as needed.
Regulatory Activities: Participates with DSS or Biometrics management in discussions with corresponding technical personnel from regulatory agencies and with investigators concerning proposed or ongoing studies.
MS or PhD in Statistics, Biostatistics or a highly related field.
At least 4-6 years (PhD) or 8-10 years (MS) of experience in pharmaceuticaldevelopment and applied statistics/statistical consulting required.
High degree of technical competence and effective oral and written communication skills.
Competent in experimental design, statistical modeling and inferential statistics; actively seeks to acquire knowledge concerning the use of new/novel statistical techniques and their biometric/ biopharmaceutical applications.
Pharmaceutical or related industry experience with clinical studies, including experience and understanding of drug development in the regulated environment preferred.
Experience in oncology is highly preferred; experience in early development (Phase 1) is highly preferred.
Ability demonstrating strong cross functional team work is required; must be able to work in a fast paced environment and change course when needed
Significant Work Activities and Conditions: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel: Yes, 5 % of the Time
Job Type: Experienced