20 matching jobs for “Biostatistical Programming Manager”

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Amgen

Biostatistical Programming Manager

Hyderabad, India 2 postings

Full time
Regular

Biostatistical Programming Manager HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Manager

Hyderabad, India

Full time
Regular

Biostatistical Programming Manager HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Manager

Hyderabad, India

Full time
Regular

Biostatistical Programming Manager HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Manager

Hyderabad, India

Full time
Regular

Biostatistical Programming Manager HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Manager

Taipei, Taiwan

Full time
Regular

… the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a Biostatistical Programming Manager in Taipei, Taiwan. Live What you will do Amgen is expanding its Global Statistical Programming (GSP) …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Manager

United States - Remote

Full time
Regular

… as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Biostatistical Programming Manager What you will do Let’s do this. Let’s change the world. In this vital role you will provide both strategic …

Added Oct 15, 2026

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Amgen

Senior Manager, Biostatistical Programming

Hyderabad, India

Full time
Regular

Senior Manager, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something …

Added Oct 15, 2026

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Amgen

Senior Manager, Biostatistical Programming

Hyderabad, India 2 postings

Full time
Regular

Senior Manager, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something …

Added Oct 15, 2026

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Amgen

Senior Manager, Biostatistical Programming

Hyderabad, India

Full time
Regular

Senior Manager, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something …

Added Oct 15, 2026

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Amgen

Senior Manager Biostatistical Programming

Taipei, Taiwan

Full time
Regular

What you will do Amgen is expanding its Global Statistical Programming (GSP) capabilities, with Amgen Taiwan playing a key role in supporting integrated delivery across regions. …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Mgr

Hyderabad, India

Full time
Regular

Biostatistical Programming Manager What you will do Let’s do this. Let’s change the world. Amgen is expanding its Global Statistical …

Added Oct 15, 2026

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Gilead Sciences

Senior Manager, Biostatistics

Parsippany, New Jersey, United States +1 location

Full time
Regular

Pay posted by employer$153,935–$199,210

… assignment, may lead projects or other activities that are non-molecule based, such as Biostatistics tools, programming, centralized analyses and reporting, etc. Where applicable, oversees and contributes to completion of all …

Added Oct 15, 2026

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Amgen

Senior Manager Information Systems

Hyderabad, India

Full time
Regular

… a highly talented team that is built for delivering high-end and innovative technologies in support of biostatistical study design and analys i s . The ideal candidate will have a proven track record of leadership in …

Added Oct 15, 2026

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IQVIA Holdings

Sr Biostatistician

Bengaluru, India

… requirements, according to Standard Operating Procedures (SOPs), for each task undertaken. Checks programming logs for cleanliness and correct processing of data. Inputs into Data Issues log and follows issues to …

Added Oct 15, 2026

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IQVIA Holdings

Statistical Programmer 2

Kochi, India +1 location

Added Oct 15, 2026

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Amgen

Senior Associate - RWE Application Development

Hyderabad, India

Full time
Regular

… of the Amgen team. Join us and transform the lives of patients while transforming your career. Sr Associate Biostatistical Programming What you will do Let’s do this. Let’s change the world. In this vital role you will Enhance and …

Added Oct 15, 2026

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IQVIA Holdings

Statistician

Beijing, China +1 location

Added Oct 15, 2026

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Thermo Fisher Scientific

Statistical Science Director

Bengaluru, India

… and therapeutic area thought leader for study design and statistical analysis issues. Serves as the project manager for contracts both standalone and cross divisional. Provides scientific strategy consultation to clients …

Added Oct 16, 2026

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Bristol-Myers Squibb

Associate Director, Biostatistics

Remote - United States - US

Full time
Regular

Pay posted by employer$189,670–$229,834

… regulated environment and to adhere to all RayzeBio guidelines and SOPs. Familiarity with statistical programming tools (e.g., SAS and/or R) and working knowledge of CDISC standards (SDTM/ADaM), with the ability to review …

Added Oct 15, 2026

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Bristol-Myers Squibb

Director, Biostatistics

Madison - Giralda - NJ - US +2 locations

Full time
Regular

Pay posted by employer$244,990–$296,867

… technical discussions. Contributes to the statistical community of practice Provides active coaching to biostatistical team members when developing solutions to problems. Effectively communicates the GBDS Mission and Vision in …

Added Oct 15, 2026

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IQVIA Holdings

Statistician

Beijing, China +1 more

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About this opportunity

Original employer description

Job Overview
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.

Essential Functions
• Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Conducts all appropriate validation requirements, according to Standard Operating Procedures (SOPs), for each task undertaken. Checks programming logs for cleanliness and correct processing of data. Inputs into Data Issues log and follows issues to appropriate resolution.
• Leadership: Perform statistical team lead role on single studies. Through this, works closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget. Build and maintain effective customer relationships, driving statistical discussions, providing support and/or guidance for statistical activities. Demonstrates and promotes efficient communication. If in lead role, runs meetings, documenting where necessary and following up on actions. Actively participates in internal project team meetings, provides timely progress updates. As a lead, will have input on estimate at completion (EAC) reporting.
• Data Management: Assist in reviewing or advising data management staff on database design, validation checks and critical data. Handles data issue resolutions. If in lead biostatistical role, handles lock and unblinding process with appropriate supervision.
• Statistical Analysis Plan (SAP) and Shells: Authors or performs quality control review (QC) of SAPs and shells. Make best use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods). May author or QC complex SAPs, under supervision if needed.
• Datasets: Writes and maintains programming specifications. Programs assigned datasets to industry standards. Handles dataset derivations and assignment.
• Tables, Listings and Figures (TLFs): Writes programming specifications for statistical analyses outputs. Programs TLFs, maximizes programming efficiency with use of tools, where applicable. Checks resulting output for format and content, and questions specification as needed. Ensures consistency across items produced.
• Timelines: Plans and documents timelines, forecasts resource needs, suggests work may be out of scope.
• Financials: Shares accountability (with resource managers) for the financial success of assigned studies. Accountable for controlling costs and maximizing revenue recognition. Responsible for sharing budget expectations with the team. Raises concerns to manager if new work or rework appears to be out of scope. Understands 'scope of work' and has an awareness of contract and budget assumptions.
• Knowledge Sharing: Helps train staff regarding operational items. Mentors junior staff. Supports colleagues and provides motivation as needed.
• Risk Management: Identifies risks to project delivery and/or quality and spends time to proactively avoid as well as proposes solutions to mitigate risks. Where possible, anticipate risks to minimize need for study level escalations.
• Other Clinical Data Interchange Standards Consortium (CDISC) requirements: Leadership: Under supervision within Compound. May perform statistical team lead role on studies within a compound. In addition to the leadership responsibilities above, also prioritizes and takes proactive approach to gain efficiencies in work across protocols.
• Study Start up: Assist with protocol development, sample size calculation, protocol and case report form (CRF) review.
• Protocol: Authors or performs quality control (QC) review of the statistical section of a protocol (making best possible use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods).
• Proposals: May be able to review and comment on proposals/budgets at a study level. May contribute to request for proposals (RFP). May be expected to present at bid defenses.
• Clinical Study Report (CSR): Reviews or drafts CSR or statistical report.
• Customer: On occasion, may serve as primary point of contact for customer. May also consult on operational topics with clients.
• Lock and Unblinding Process: Handles 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.
• Other Responsibilities: As defined on ad-hoc basis by managers. May assist with cross functional collaboration.

Qualifications
• Bachelor's Degree Biostatistics or related field and 3 - 5 years relevant experience Req Or
• Master's Degree Biostatistics or related field and 3-5 years relevant experience Req Or
• Ph.D. Biostatistics or related field and 1 year relevant experience Req
• Typically requires 3-5 years of prior relevant experience, or equivalent combination of education, training and experience.
• Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.
• Excellent written and oral communication skills including grammatical/technical writing skills.
• Excellent attention and accuracy with details.
• 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 individual initiative.
• Strong organizing skills.
• Strong working knowledge of SAS computing package.
• Familiarity with other relevant statistical computing packages such as nQuery.
• Strong commitment to quality.
• Ability to effectively manage multiple tasks and projects.
• Ability to lead and co-ordinate small teams.
• Ability to solve moderately complex problems.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium CDISC/ADaM).

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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