Job Overview:
As an Associate Director, Biostatistics, you will join one of the largest, award winning and innovative Biostatistics departments and will be given access to cutting-edge in-house technology.
With global visibility, provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying advanced statistical methods to project work.
Serve as a resource for the department, ensuring scientific integrity in the application of statistical methodology to clinical trials.
Assist the Director in strategic planning and resource allocation for the department.
Participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.
Assist the Director in proposal development, project allocations, budget projections, and client presentation.
Key Responsibilities:
- Completes and reviews more complex assigned tasks with a focus on accuracy
- Leadership:
- Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company.
- Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses.
- Represent clients at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee
- Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication
- Participate as high level lead biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or NDA sections, as required
- Leading studies at an operational level until SAP writing begins
- Drive operational pieces of the business segment (e.g. resource management for a business segment, recruitment management for a business segment)
- Provide expert review of process and initiate methodology development work with regards to statistical standards and validation procedures
- Consults on operational/statistical/therapeutic area topics
- Performs as a recognized subject matter expert (SME) who defines training needs and maps out strategies for Director and Senior Directors to approve
- Identifies risks to project delivery and/or quality, leads in a way that risks are avoided
- Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions
- Handles most study level escalations that that might impact the account relationship
- Escalates for support to business segment owners/client owners/managers
- Lock and Unblinding Process:
- Leads the database lock and unblinding process
- Participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules)
- Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures and statistical sections for complex and/or integrated reports)
- Provide expert input into data management deliverables (i.e. database design, CRF design, validation checks and critical data)
- Provide expert review of ADaM reviewers guide (ADRG)
- Perform senior biostatistician review (SBR)
- Produce or perform quality control review of sample size calculations for complex studies
- Share accountability (with resource managers) for the financial success of studies
- Accountable for controlling costs and maximizing revenue recognition
- Also responsible for sharing budget expectations with team
- Understanding of what goes into a budget, how to propose adjustments, and be able to discuss budget assumptions with clients as well as the ability to understand and discuss pricing models
- Participate in sales meetings
- Able to review and write proposals/budgets at a study/submission level ability to understand of what goes into a budget, how to propose adjustments, and be able to discuss budget assumptions with clients as well as the ability to understand and discuss pricing models
Requirements:
- BSc or MSc degree in Biostatistics or related field and 10+ years’ relevant experience within the life-science industry
- Familiarity with complex statistical methods that apply to Phase I-IV clinical trials
- In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Familiarity with moderately complex statistical methods that apply to applicable clinical trials
- Strong working knowledge of SAS
- Working knowledge of relevant Data Standards (such as CDISC/ADaM)
From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.
What is in it for you?
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance
JOIN US
Embrace your curiosity and grow your career in an exciting environment where development is a priority.
Think boldly and disrupt conventional thinking.
Enjoy what you do.
Whatever your career goals, we are here to ensure you get there!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com