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Assistant Director, Clinical Statistics

AbbVie

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Location:
Chicago, IL
Posted Date:
7/24/2014
Position Type:
Full time
Job Code:
13000004OA
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:

Job Description

Statistics is responsible for providing services in the area of biostatistics and mathematics to all corporate divisions. These services are supplied in the context of a cooperative, project-oriented effort and included statistical planning and scientific input in general planning and execution of clinical trials, pre-clinical trials and other experiments as well as integration of all scientific expertise and available technologies to provide statistical analysis of the data from these trials. These services also include the generation of scientific reports summarizing the trial or experimental results for communication to regulatory agencies and scientific audiences.  We have an exciting opportunity for an Assistant Director, Statistics or Senior Manager, Statistics based in North Chicago, IL.


 


Key Responsibilties:


  • Provides scientific and statistical expertise through own efforts and those of her/his staff (if appropriate) for drug discovery or development strategies for assigned project; for the design, analysis, and reporting of scientific research trials; and for interacting with regulatory agencies regarding the results of these activities.

 


Protocol Development: 


  • 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

 


Database Activities:


  • 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

 


Statistical Analyses:


  • 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

  • Represents Data and Statistical Sciences (DSS) or Biometrics on project issues at management review meetings and project team meetings

  • Provides in-depth scientific/statistical review for scientific reports and publications

  • Ensures the accuracy of the statistical component of scientific reports and/or publications with high quality

 


Consultation:


  • Partners with multiple stakeholders to develop scientifically appropriate development strategies for assigned drug discovery or development project

  • Effectively plans and coordinates statistical resources to best meet assigned project priorities

  • Works with Director and appropriate administrative staff to manage alternative resources (i.e., consultants, CROs, interns, temporary staff) to satisfy needs for assigned project

  • Interacts with relevant stakeholders to ensure that appropriate statistical methods are adequately and consistently applied in all scientific and regulatory documents, presentations, and publications

  • Provides scientific/statistical insight in addressing questions from clients, and proposes novel solutions to technical issues

  • Independently pursues analyses suggested by the data, including the pursuit of statistical knowledge needed to address the scientific issue

  • In collaboration with Statistical Programming or their designee, ensures that all internal and external statistical software used in the performance of analyses defined in SAPs or scientific research plans are efficient, validated, and meet internal SOPs and external regulatory requirements

  • Acts as the liaison for statistical issues on AbbVie collaborative studies with outside universities, government agencies, steering and/or data monitoring committees, joint ventures or licensing activities

  • Builds external scientific contacts which foster professional development and promote the reputation of the department

  • Demonstrates good understanding of scientific research designs, worldwide regulatory requirements and commercial aspects of drug development

  • Critically reviews regulatory submission documents for assigned drug discovery or drug development project

  • Effectively and persuasively presents statistical concepts, evidence, interpretations, and logical arguments to the project team, management, regulatory agencies, and scientists

 


Project Team Involvement:


  • Partners with Clinical and Regulatory to develop scientifically appropriate development strategies for assigned project

  • Represents DSS or Biometrics on project team(s) to provide functional area input to compound/drug development and ensures alignment with functional management

  • Leads the communication between assigned project team(s) and DSS/Biometrics functional area to ensure timely communication of project team updates, proper statistical strategies, and alignment of priorities between the project team and functional management

 


Training, Supervising, Mentoring:


  • In conjunction with Associate Director and/or Director, coordinates statistical support for assigned drug discovery or development project

  • Effectively mentors other development stakeholders with regards to statistical methodology and departmental operations

  • Mentors and/or manages personnel when appropriate by delegating assignments, reviewing activities and defining/ensuring review of deliverables so that projects are completed on time with high quality

  • Fosters the scientific development of staff

  • Participates in department seminars, short courses, and the publication presentation of scientific articles

  • Works with Associate Director and/or Director to arrange training opportunities for staff to facilitate their timely career development

  • Works with Director and/or appropriate administrative management to recruit qualified statisticians to the organization

  • Ensures that staff (if appropriate) and self are compliant with training requirements.  Demonstrates a high degree of responsibility in maintaining DSS / Biometrics standards, GxP compliance, and best operating practices for staff (if appropriate) and self

 


Project Coordination / Regulatory Activities: 


  • Coordinates statistical resources within and across sites to effectively utilize resources

  • Reviews key decisions impacting project timelines with department management

  • Has a strategic focus on assigned drug discovery or development project and optimizes execution

  • Works with Director to build relationships between DSS / Biometrics and outside investigators and medical/scientific experts

  • Ensures that all applicable regulatory requirements for work processes are met

  • Participates in discussions with regulatory agencies as needed

  • Consistently demonstrates excellent record of achievement with respect to DSS / Biometrics and business objectives

 


 


 


 

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Requirements

Position will be hired based on level of experience


 


Basic:


 


For Assistant Director:


  • M.S./Ph.D. in Statistics, Biostatistics or a related field

  • At least 6-8 yrs (PhD) or 10-12 yrs (MS) experience in pharmaceutical development and applied statistics/statistical consulting

  • Project lead experience required

  • Broad knowledge of statistical methodology and global regulatory requirements, expertise in drug discovery or development, and an understanding of commercial aspects of drug development

  • Experience interacting with regulatory agencies highly desirable

  • Excellent communication skills, both oral and written

  • Jointly with other project team members, develops and evaluates options for meeting project team goals under time and resource constraints

  • Proposes and evaluates options for responding to questions from internal and external sources, including regulatory agencies

  • Implements the agreed upon solution after discussion with other stakeholders.Identifies opportunities for, and leads teams for process improvement initiatives

  • Actively participates in risk assessment and development of contingency plans

  • Productive in relevant statistical research and problem solving

 


For Sr Manager, Statistics:


  • 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 pharmaceutical development 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 nonclinical, clinical or pharmacology studies, as appropriate, including experience and understanding of drug development in the regulated environment preferred

  • Works collaboratively with function management and multiple stakeholders to develop strategies for addressing issues/requirements that arise in clinical, nonclinical or pharmacology programs, as appropriate

Key Leadership Competencies:


  • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance

  • Learns fast, grasps the 'essence' and can change the course quickly where indicated

  • Raises the bar and is never satisfied with the status quo

  • Creates a learning environment, open to suggestions and experimentation for improvement

  • Embraces the ideas of others, nurtures innovation and manages innovation to reality

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