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7 PHASTAR Jobs

Principal Statistical Programmer

5-10 years

Remote

1 vacancy

Principal Statistical Programmer

PHASTAR

posted 14hr ago

Job Description

Employees may be required to perform some or all of the following:
Program and validate datasets and SDTMs, including complex efficacy, labs, etc.
Become independent technical expert
Program complex non efficacy outputs/ figures
Perform Senior Review and Deliver QC of non- statistical output
Become involved in developing the standard macro library and take responsibility to implement standard macros within a study
Validate and perform User Acceptance Testing (UAT) on standard macros
Identify macros requirements, communicate and perform training
Create, QC and update complex dataset specifications (including efficacy) for single/ multiple studies, ISS/ISEs, etc
Implement and coordinate development and maintenance of PHASTAR standard specifications
Be an SDTM and ADAM expert providing consultancy, advice and training
Be an CRT expert providing consultancy, advice and training
Be aware of up and coming changes to CRT and define.xml standards and regulatory guidelines and requirements
Implement and coordinate the development and maintenance of PHASTAR CRT tools
Become familiar with and follow study documentation
Initiating projects and ideas for furthering programming development
Ensure the principles in the PHASTAR checklist are followed rigorously
Develop archiving systems and processes
Act as a Lead programmer on multiple studies and project, ensuring quality and timely delivery
Liaise with Study Statistician and Project Manager regarding resourcing and deliverables
Responsible for study level resources
Attend and input to company resourcing meeting
Point of contact for programming issues for the team, proactively ensuring everything is working cohesively
Persuade stakeholders to follow best practice within a trial
Develop and deliver company-wide training as and when required
Identify areas where new processes are required
Create, review and update processes and SOPs
Take responsibility for study compliance with SOPs and processes

Qualifications

  • BSc or above in mathematics, science, or IT related discipline.
  • Experience working on clinical trials within a CRO/pharmaceutical environment.
  • Excellent proven end to end programming experience including SDTM, ADaM and TLFs with solid experience of validating/reviewing outputs
  • Strong QC ability across ADaMs and TLFs predominantly but good SDTM experience needed
  • Ability to work independently and link in with client for work assignments, updated FSP manager on progress/timelines/challenges and feedback QC comments to third party vendor
  • Must be able to work autonomously as there is no overlap with client teams based in US for day-to-day communication. Has to feel comfortable prioritising tasks and being able to investigate issues and suggest solutions
and timely delivery
Liaise with Study Statistician and Project Manager regarding resourcing and deliverables
Responsible for study level resources
Attend and input to company resourcing meeting
Point of contact for programming issues for the team, proactively ensuring everything is working cohesively
Persuade stakeholders to follow best practice within a trial
Develop and deliver company-wide training as and when required
Identify areas where new processes are required
Create, review and update processes and SOPs
Take responsibility for study compliance with SOPs and processe

Employment Type: Full Time, Permanent

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What people at PHASTAR are saying

What PHASTAR employees are saying about work life

based on 6 employees
100%
80%
100%
Flexible timing
Monday to Friday
No travel
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PHASTAR Benefits

Free Transport
Child care
Gymnasium
Cafeteria
Work From Home
Free Food +6 more
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