Senior Biostatistician

Closing date
30 Sep 2020

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Data Management / Statistics, Biostatistics
Full Time
Contract Type
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IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.



IQVIA is looking to appoint Senior Biostatistician to develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports. Accountable for controlling costs and maximizing revenue recognition. Provide training, guidance and mentorship to lower level and new staff.


Production of High-Quality Deliverables

Completes and reviews more complex assigned tasks on time/early with a focus on accuracy.  If in a team lead role, oversees team with same expectations.  Conducts all appropriate validation requirements, according to SOPs, for each task undertaken. Checks data for cleanliness and correct processing. Inputs into Data Issues log and follows issues to appropriate resolution.


Perform statistical team lead role on complex studies and/or within a compound.  Through this, works with the team to ensure high quality deliverables, delivers on time within budget, ensures compliance with SOPs, ensure consistency across teams and across protocols, manages/delegates data quality issue resolutions.  As a lead of groups of studies within a compound, also prioritizes and leads proactively to gain efficiencies in work across protocols and deliver on time across multiple protocols.  May also serve in statistical project oversight role for simple studies. Responsible for driving statistical discussions, actively participates in internal project team meetings, provides timely progress updates.  In a lead role, runs meetings, provides timeline updates, assess resource needs, documents, and follows up on actions.  Supports colleagues and provides motivation.

Data Management

Reviews and advises data management staff on CRF and database design, validation checks and critical data. Leads data issue resolutions. If in lead biostatistical role, handles lock and unblinding process with appropriate supervision.

Study Start up 

Authors/QC statistical section of a protocol, with authors making best possible use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods). Produces/QCs sample size calculations.  Covers complex studies

Statistical Analysis Plan (SAP) and Shells  

Authors and/or performs quality control review (QC) of SAPs and shells, makes best possible use of resources. Shares own expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods).


Writes and maintains programming specifications, with a focus on efficacy.  Manages dataset derivations and assignment.  May program analysis datasets, including complex domains and derivations. Handles analysis set derivations and assignment.

Tables, Listings and Figures (TLFs)

Writes programming specifications for statistical analyses outputs.  Checks outputs for format and content. Ensures consistency across items produced.  May program complex Tables/Figures (Main or QC), using Bios tools where applicable.  

Clinical Study Report (CSR) 

Reviews or drafts CSR or statistical report, under supervision as needed.


Plans, documents, and negotiates timelines, forecasts resource needs, identifies out of scope work.

Lock and Unblinding Process 

Leads the database lock and unblinding process. May participate on the biostatistics randomization team (drafts randomization specifications and/or reduce or perform quality control (QC) review of randomization schedules).  May serve as unblinded lead statistician.


Serves as point of contact for customer for individual studies and responsible for building and maintaining effective client relationships.  Consults on operational/statistical topics with clients.

Statistical Expertise 

Provide expert statistical input into review of statistical deliverables (i.e. analysis plans, table shells, programming and table specifications, data review, tables, listings, figures and statistical sections for integrated reports) and data management deliverables (i.e. database design, CRF design, validation checks and critical data).  Provide expert review of ADaM reviewers guide (ADRG).  May perform senior biostatistician review (SBR), under supervision.


Shares accountability (with therapeutic area leads and Director) for the financial success of assigned studies. Accountable for controlling costs and maximizing revenue recognition. Also responsible for sharing budget expectations with the team.  Responsible for negotiating out of scope work.  Understands 'scope of work', contract, and budget assumptions.  Project leads collaborate on creation/revisions of Estimate at Completion (EAC) reporting.

Knowledge Sharing  

Helps train staff regarding operational items.  Provides training at a department/site/team/Global level.  May be expected to act as subject matter expert (SME).  Mentors senior staff, including offshore.

Risk Management 

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. Handles most study level escalations that do not impact the account relationship and escalates for support to business segment owners/client owners/managers.


Able to review and comment on proposals/budgets at a study level.  Contributes to request for proposals (RFP).  Presents at bid defenses.

Other Responsibilities

 As defined on ad-hoc basis by managers. May assist with cross functional collaboration. 


Join Us



Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.



Forge a career with greater purpose, make an impact, and never stop learning.


At IQVIA™, we are committed to advancing human health and delivering real value and outcomes for customers and patients. We view each day as another opportunity to find new solutions and enable the next breakthrough.

IQVIA is a leading global provider of information, innovative technology solutions and contract research services dedicated to using analytics and science to help healthcare stakeholders find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA has approximately 55,000 employees worldwide.

Please visit our Careers Hub on PharmiWeb.Jobs:

Contact Us
  • 210 Pentonville Road
  • London
  • N1 9JY
  • GB
  • +44 (0) 20 3075 5000
  • Mini-site: IQVIA
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