

Senior Director, Data Science
β - Featured Role | Apply direct with Data Freelance Hub
This role is for a Senior Director, Data Science, with a contract length of more than 6 months and a pay rate of $272,000 - $343,000 per year. Key skills required include SAS programming, CDISC standards, and experience in retinal development.
π - Country
United States
π± - Currency
$ USD
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π° - Day rate
1559.0909090909
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ποΈ - Date discovered
August 27, 2025
π - Project duration
More than 6 months
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ποΈ - Location type
Unknown
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π - Contract type
Unknown
-
π - Security clearance
Unknown
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π - Location detailed
United States
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π§ - Skills detailed
#Data Science #IP (Internet Protocol) #Datasets #SAS #Programming #Base #Strategy #ADaM (Analysis Data Model) #CDISC (Clinical Data Interchange Standards Consortium)
Role description
Attention recruitment agencies: All agency inquiries are vetted through 4DMTβs internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.
4DMT is a clinical-stage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines. We seek to unlock the full potential of gene therapy using our platform, Therapeutic Vector Evolution (TVE), which combines the power of directed evolution with our approximately one billion synthetic AAV capsid-derived sequences to invent evolved vectors for use in our products. We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles. These profiles will allow us to treat a broad range of large market diseases, unlike most current genetic medicines that generally focus on rare or small market diseases.
Company Differentiators:
β’ Fully integrated clinical-phase company with internal manufacturing
β’ Demonstrated ability to move rapidly from idea to IND
β’ Robust technology and IP foundation, including our TVE and manufacturing platforms
β’ Initial product safety and efficacy data substantiates the value of our platforms
β’ Opportunities to expand to other indications and modalities within genetic medicine
General Summary
The incumbent provides strategic statistical input to and oversees all statistical aspects of assigned programs; drives cross-functional collaboration and decision making for program(s); oversees the performance of Contract Research Organizations (CROs); develop and mentor other statisticians.
MAJOR DUTIES & RESPONSIBILITIES:
β’ Ensures expert level contribution to strategy (design, analysis/synthesis, interpretation and reporting, health authority response, influence and implement publication strategy, quantitative decision making) for critical studies in a program
β’ Leads collaborations with clinical, regulatory and other strategic functions to drive quantitative decision making and enables successful impact on robust drug development plans
β’ Maintains indication specific standards with respect to key variables, variable definitions, statistical methods, data structures and presentation of results.
β’ Provides oversight and guidance to staff members within 4DMT and in CROs in completing high quality study deliverables according to agreed timelines following quality standards.
β’ Leads and/or participates in the development and review of Policies, SOPs and other controlled documents for process improvement and operational efficiency.
β’ Supports the preparation and validation of statistical analyses for use in regulatory documents and scientific articles. Support internal ad-hoc and exploratory analysis.
β’ Plays a critical role in shaping team development and contributing to departmental strategy.
β’ Stays abreast of and contributes to scientific advances in the field.
QUALIFICATIONS:
Education:
β’ 10+ years of pharmaceutical industry experience with a PhD, or 12+ years with an MS.
Experience:
β’ Hands-on familiarity with common and advanced statistical methodology.
β’ Hands-on experience working with CDISC standards and programming based on raw datasets, SDTM, and ADaM datasets.
Other Qualifications/Skills:
β’ Strong knowledge of SAS programming concepts and techniques in the pharmaceutical; proficiency in tools such as SAS, EAST, and nQuery.
β’ Knowledge/experience of Retinal development, including global regulatory requirements and design and analysis of non-inferiority trials
Travel: Minimal 5%
Physical Requirements and Working Conditions:
β’ Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.
β’ Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
β’ Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).
Base salary compensation range: $272,000/yr - $343,000/yr
4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
Attention recruitment agencies: All agency inquiries are vetted through 4DMTβs internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.
4DMT is a clinical-stage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines. We seek to unlock the full potential of gene therapy using our platform, Therapeutic Vector Evolution (TVE), which combines the power of directed evolution with our approximately one billion synthetic AAV capsid-derived sequences to invent evolved vectors for use in our products. We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles. These profiles will allow us to treat a broad range of large market diseases, unlike most current genetic medicines that generally focus on rare or small market diseases.
Company Differentiators:
β’ Fully integrated clinical-phase company with internal manufacturing
β’ Demonstrated ability to move rapidly from idea to IND
β’ Robust technology and IP foundation, including our TVE and manufacturing platforms
β’ Initial product safety and efficacy data substantiates the value of our platforms
β’ Opportunities to expand to other indications and modalities within genetic medicine
General Summary
The incumbent provides strategic statistical input to and oversees all statistical aspects of assigned programs; drives cross-functional collaboration and decision making for program(s); oversees the performance of Contract Research Organizations (CROs); develop and mentor other statisticians.
MAJOR DUTIES & RESPONSIBILITIES:
β’ Ensures expert level contribution to strategy (design, analysis/synthesis, interpretation and reporting, health authority response, influence and implement publication strategy, quantitative decision making) for critical studies in a program
β’ Leads collaborations with clinical, regulatory and other strategic functions to drive quantitative decision making and enables successful impact on robust drug development plans
β’ Maintains indication specific standards with respect to key variables, variable definitions, statistical methods, data structures and presentation of results.
β’ Provides oversight and guidance to staff members within 4DMT and in CROs in completing high quality study deliverables according to agreed timelines following quality standards.
β’ Leads and/or participates in the development and review of Policies, SOPs and other controlled documents for process improvement and operational efficiency.
β’ Supports the preparation and validation of statistical analyses for use in regulatory documents and scientific articles. Support internal ad-hoc and exploratory analysis.
β’ Plays a critical role in shaping team development and contributing to departmental strategy.
β’ Stays abreast of and contributes to scientific advances in the field.
QUALIFICATIONS:
Education:
β’ 10+ years of pharmaceutical industry experience with a PhD, or 12+ years with an MS.
Experience:
β’ Hands-on familiarity with common and advanced statistical methodology.
β’ Hands-on experience working with CDISC standards and programming based on raw datasets, SDTM, and ADaM datasets.
Other Qualifications/Skills:
β’ Strong knowledge of SAS programming concepts and techniques in the pharmaceutical; proficiency in tools such as SAS, EAST, and nQuery.
β’ Knowledge/experience of Retinal development, including global regulatory requirements and design and analysis of non-inferiority trials
Travel: Minimal 5%
Physical Requirements and Working Conditions:
β’ Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.
β’ Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
β’ Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).
Base salary compensation range: $272,000/yr - $343,000/yr
4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities