Current jobs related to Manager / Senior Manager, Statistics (Oncology) - South San Francisco - AbbVie


  • San Francisco, United States Meet Recruitment Limited Full time

    Title: Senior Manager, Statistical Programming Summary: My clinical stage biopharma client is seeking an experienced SAS programmer to fill an Senior Manager of Statistical programming opening. This will be hands-on programming for clinical studies for exploratory analyses, regulatory responses, and defense activities. Position Overview: Conduct...


  • San Francisco, California, United States Meet Recruitment Limited Full time

    Job Title: Senior Manager, Statistical ProgrammingJob Summary:Meet Recruitment Limited is seeking an experienced Senior Manager of Statistical Programming to join our team. As a key member of our clinical stage biopharma client, you will be responsible for hands-on programming for clinical studies, including exploratory analyses, regulatory responses, and...

  • Director, Statistics

    4 months ago


    South San Francisco, United States AbbVie Full time

    Company Description   AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and...


  • South San Francisco, California, United States Annexon Bioscience Full time

    Work Location Corporate Headquarters - Hybrid Position Overview We are in search of a proactive and seasoned Senior Vice President of Statistical Sciences to spearhead our Statistical Sciences division. The ideal candidate will deliver strategic leadership and operational management for all facets of biostatistics, statistical programming, modeling,...


  • San Francisco, California, United States Elan Solutions LLC Full time

    Job OverviewPosition: Manager of Statistical Programming (Full Time, Remote)Company: Elan Solutions LLCSalary Range: $150,000 - $153,800Essential Qualifications:Minimum 5 years of experience in a Contract Research Organization (CRO)At least 3 years of experience as a Study Lead3+ years in Personnel ManagementAbility to work within Pacific Time ZoneExperience...


  • South San Francisco, United States Meet Full time

    Senior CTM - SF Bay Area OncologyJoin a rapidly growing biotech company focused in oncology research. This company fosters a highly collaborative environment, as well as allowing for high levels of professional growth. The team is looking for an experienced Senior Clinical Trial manager to lead their clinical trials. This is a high-visibility role where you...


  • South San Francisco, United States Meet Full time

    Senior CTM - SF Bay Area OncologyJoin a rapidly growing biotech company focused in oncology research. This company fosters a highly collaborative environment, as well as allowing for high levels of professional growth. The team is looking for an experienced Senior Clinical Trial manager to lead their clinical trials. This is a high-visibility role where you...


  • San Francisco, California, United States Seasons Utah Manager LLC Full time

    Unlock Your Potential as a Team LeaderAre you a motivated and results-driven individual looking to take your career to the next level? As a Team Leader at Seasons Utah Manager LLC, you will have the opportunity to develop your leadership skills and make a real impact on our team's success.Key Responsibilities:Lead and motivate a high-performing team to...


  • San Francisco, United States Warman O'Brien Full time

    SAS Programmer (Oncology Focus) | Small CRO | Full-Time PermanentWe are seeking an experienced SAS Programmer with a strong background in NDA filings, ISS, and ISE to join our small CRO client who are specialists within Data Science. This is a lead role, requiring someone who can provide technical leadership and has a deep understanding of oncology data....


  • San Antonio, Texas, United States US Oncology, Inc Full time

    Senior Registered Nurse (RN) - OncologyAn exceptional opportunity awaits for a Senior Registered Nurse (RN) to become a vital member of the team at US Oncology, Inc. This role is designed for those passionate about providing exemplary care in the oncology field.This full-time position offers a structured Monday to Friday schedule, ensuring a work-life...


  • San Francisco, United States AbbVie Full time

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan...


  • San Francisco, United States AbbVie Full time

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan...


  • South San Francisco, California, United States Meet Full time

    {"title": "Director of Statistical Programming", "content": "Job SummaryThe Director of Statistical Programming will provide strategic oversight, planning, and execution of the statistical programming function to support an expanding portfolio of clinical development programs. This role will collaborate with key stakeholders across Biometrics, Data...


  • South San Francisco, United States Meet Full time

    Director, Statistical Programming - Head of Statistical Programming(Hybrid 3 days per week in South San Francisco, CA)Position OverviewThe Director of Statistical Programming will provide strategic oversight, planning, and execution of the statistical programming function to support an expanding portfolio of clinical development programs. This role will...


  • San Francisco, California, United States Barrington James Full time

    Director of Statistical Programming - Biotech IndustryWe are partnering with a rare disease focused Biotech company to seek a Director of Statistical Programming.The company is focused on a rare disease with significant unmet medical needs, offering a unique opportunity to make a meaningful impact.The team is experienced and collaborative, with two...


  • San Francisco, California, United States Barrington James Full time

    Biotech Statistical Programming OpportunityWe are partnering with a rare disease focused Biotech in San Francisco to find a skilled Statistical Programming professional.The company is focused on a rare disease with unmet medical needs, offering a chance to make a meaningful impact.The team is experienced, with two Director-level programmers, and you will...


  • San Francisco, California, United States Meet Full time

    Meet the Challenge of Groundbreaking Oncology Research **Senior Clinical Trial Manager - SF Bay Area Oncology** We are seeking an experienced Senior Clinical Trial Manager to lead our clinical trials in oncology research. As a key member of our team, you will work closely with cross-functional teams and external partners to ensure the successful execution...


  • San Diego, California, United States WuXi AppTec Full time

    Senior Statistical Consultant - Biopharmaceutical SectorWuXi AppTec is in search of a Senior Statistical Consultant to deliver high-level statistical consulting services to our partners in the biopharmaceutical sector. The successful candidate will possess a robust foundation in statistical techniques and clinical trial architecture, along with experience in...


  • San Antonio, Texas, United States US Oncology, Inc Full time

    Job SummaryUS Oncology, Inc is seeking a highly skilled and experienced Senior Registered Nurse to join our team. As a key member of our Oncology department, you will be responsible for providing exceptional patient care and contributing to the delivery of high-quality, evidence-based cancer care.Key ResponsibilitiesPlan, implement, and evaluate patient care...


  • San Francisco, California, United States Meet Full time

    Senior Clinical Trials Manager - Oncology ResearchMeet a rapidly growing biotech company focused on developing innovative oncology treatments. This company fosters a collaborative environment, allowing for high levels of professional growth and development. The team is seeking an experienced Senior Clinical Trials Manager to lead their clinical trials,...

Manager / Senior Manager, Statistics (Oncology)

4 months ago


South San Francisco, United States AbbVie Full time
Job DescriptionJob DescriptionCompany Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. 

Job Description

Purpose:

The Senior Manager, Statistics provides statistical leadership to support the research and development organization for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Senior Manager works independently in partnership with experts in multiple disciplines to advance medicines to our patients.

description: 

 

Responsibilities:

  • Protocols: Explore and select study designs aligned with Project Team strategy and goals. Provide sample-size, develop randomization specifications, and independently write statistical analysis plans to address study objectives. Ensure alignment of protocol with project and functional standards. Conduct quality review of protocol. Implement randomization schedules as planned with Interactive Response Technology vendor, Global Drug Supply Management, and other partners.
  • Database Activities: Ensure data collection instruments are adequate and data collection is free of bias. Ensure database design satisfies statistical analysis requirements. Contribute to data monitoring plans. Develop and implement project-specific data standards. Identify and report data issues or violation of study assumptions. Guide programmers and data managers in preparing for database lock. Ensure accuracy of data released for statistical analysis.
  • Statistical Analyses: Independently evaluate alternative complex or novel statistical approaches, make recommendations, approve, and implement. Influence non-statisticians to accept approach. Develop analysis plans ensuring statistical methods are appropriate with detail for programming. Ensure internal consistency of analysis plans. Perform statistical analyses per the SAP. Determine the need for development of novel statistical methodology.
  • Reports and Publications: With project team, develop strategy for data presentation and inference. Independently write statistical methods and other sections of protocols, publications, etc., ensuring document templates followed. Identify and implement corrections to flaws in statistical interpretation. Collaborate in publication of scientific research. Ensure analyses conducted as planned with accuracy and internal consistency of writing including tables, listings and figures.
  • Consultation: Work collaboratively with multi-function teams per agreed timelines. Timely inform management on important scientific/statistical issues that may arise. Provide responses to questions from clients and independently pursue analyses suggested by data. Effectively and persuasively present statistical concepts, evidence, assessment of risks and impacts. Demonstrate an understanding of drug development principles.
  • External Engagement: Act as the liaison for statistical and operational issues on PCYC collaborative studies with Academic and Contract Research Organizations. Communicate with statisticians outside PCYC concerning technical issues, building external scientific contacts, fostering professional development, and promoting the reputation of the department.
  • Project Team Involvement: Represent the department on project team(s) to provide functional area input to compound/drug development. Serve as a liaison between the project team and the department to ensure timely communication of project team updates, proper statistical strategies, and alignment of decisions/priorities between the project team and functional area.
  • Training and Mentoring: Maintain technical skills and increase knowledge of new statistical methods and areas of application through scientific literature and professional meeting attendance. Present own research or review of literature at meetings. Participate in departmental activities including recruiting, training/mentoring, research efforts, and cross-functional collaborations, as needed.
  • Regulatory Activities: Participate with department management in discussions with corresponding technical personnel from regulatory agencies and with investigators concerning proposed or ongoing studies.
  • Compliance: Compliant with applicable corporate and divisional policies, procedures, and cultural values. Maintain up-to-date knowledge of Standard Operating Procedures and working practices relevant to managers and the Statistics function. Responsibly maintain department standards, GxP compliance, and best operating practices. Complete all assigned training on time.
Qualifications

This position can be hired at the Manager or Sr. Manager level dependent on relevant experience and education. 

Qualifications for Manager, Statistics:

 

  • MS (with 6+ years of experience) or PhD (with 2+ years of experience) in Statistics, Biostatistics, or a highly related field.
  • High degree of technical competence and effective communication skills, both oral and written
  • Able to perform statistical computations and simulations.
  • Able to identify data or analytical issues and assist with providing solutions by either applying own skills and knowledge or seeking help from others.
  • Able to build strong relationships with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo.
  • Pharmaceutical or related industry knowledge desired, including experience and understanding of drug development and life-cycle management in the regulated environment.

Qualifications for Sr. Manager, Statistics:

  • MS (with 8+ years of experience) or PhD (with 4+ years of experience) in Statistics, Biostatistics, or a highly related field.
  • High degree of technical competence and effective communication skills, both oral and written
  • Able to identify data or analytical issues and assist with providing solutions by either applying own skills and knowledge or seeking help from others.
  • Able to manage project timeline and quality of deliverables.
  • Able to build strong relationships with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo.
  • Have strong leadership skills and experience in working/managing cross-cultural or oversea teams.
  • Pharmaceutical or related industry knowledge desired, including experience and understanding of drug development and life-cycle management in the regulated environment.
  • Some experience supporting safety-related projects (eg, ISS, benefit-risk assessment, signal detection) is preferred

 



Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

  • This job is eligible to participate in our short-term incentive programs. ​

  • This job is eligible to participate in our long-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. 

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.