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Principal Statistician

Psicro · Remote, REMOTE, United States · Remote · Active · SmartRecruiters

Job facts

FieldValue
CompanyPsicro
TitlePrincipal Statistician
Normalized title-
Department / teamData Management, Statistics, IT
LocationREMOTE, United States
Work modelRemote / Remote
Employment typeFull Time
Salary-
Statusactive
ATS providerSmartRecruiters
Posted / first seen2026-03-27 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Psicro.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Department jobsActive postings in Data Management, Statistics, IT.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyPsicro
Source2a57b066-6d90-4457-bc69-3b485bbafd80
ATS providerSmartRecruiters

Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead. In this role, you will: Act as a communication line for project teams, clients, vendors and internal team on statistical questions Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents Review statistical deliverables such as tables, figures, listings and analysis datasets Conduct departmental induction course and project-specific training for statisticians and SAS programmers Prepare for and attend internal and external study audits pertinent to Statistics Participate in preparation of internal/external audits follow up Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department Liaise with DM on statistical questions related to data issues Participate in bid defense and in kick-off meetings Lead teams of SAS programmers and/or statisticians on the project level MSc in Statistics or equivalent Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research Expert knowledge and understanding of the SAS programming Expert knowledge and understanding of CDISC ADaM standard Expert knowledge and understanding of adaptive designs Expert knowledge and understanding of sample size calculation Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH) Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies Strong presentation and communication skills Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.

Full job record

Job IDc057eb831084d9c3fd5e280a77b87749adcbe5db
Org ID09ee3685-cc0c-4268-bc4c-753b2a72bac7
Source ID2a57b066-6d90-4457-bc69-3b485bbafd80
Board ID2a57b066-6d90-4457-bc69-3b485bbafd80
Providersmartrecruiters
Provider Job Key744000117395445
TitlePrincipal Statistician
Normalized Title
Statusactive
Activeyes
Location TextRemote, REMOTE, United States
DepartmentData Management, Statistics, IT
Team
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
RegionREMOTE
City
Salary RawWe are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead. In this role, you will: Act as a communication line for project teams, clients, vendors and internal team on statistical questions Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents Review statistical deliverables such as tables, figures, listings and analysis datasets Conduct departmental induction course and project-specific training for statisticians and SAS programmers Prepare for and attend internal and external study audits pertinent to Statistics Participate in preparation of internal/external audits follow up Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department Liaise with DM on statistical questions related to data issues Participate in bid defense and in kick-off meetings Lead teams of SAS programmers and/or statisticians on the project level MSc in Statistics or equivalent Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research Expert knowledge and understanding of the SAS programming Expert knowledge and understanding of CDISC ADaM standard Expert knowledge and understanding of adaptive designs Expert knowledge and understanding of sample size calculation Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH) Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies Strong presentation and communication skills Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://jobs.smartrecruiters.com/PSICRO/744000117395445-principal-statistician
Apply URLhttps://jobs.smartrecruiters.com/PSICRO/744000117395445-principal-statistician?oga=true
First Seen At2026-05-31 17:36:56Z
Last Seen At2026-06-06 19:44:14Z
Last Checked At2026-06-06 19:44:14Z
Last Changed At2026-05-31 17:36:56Z
Inactive At
Source Posted At2026-03-27 20:13:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=psicro/date=2026-06-06/2026-06-06T19-44-10-643Z-5b05a0ec068b568c8e600a1146df1f50ddc8569c8f796facd7bdce3d9e509929.json
Event Fields
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  "last_changed_at": "2026-05-31T17:36:56.970Z",
  "active_status": "active"
}
Parsed Structured
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Extensions
{}
Native Structured
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