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Senior/Principal Statistician

Key Facts

Remote From: 
Full time
English

Other Skills

  • Detail Oriented
  • Teamwork
  • Communication

Roles & Responsibilities

  • PhD or MSc in Biostatistics/Statistics or a closely related field
  • Extensive CDISC experience (SDTMs and ADaMs)
  • Proficient in SAS; R experience is advantageous
  • Experience as a Lead Statistician and with SAP/shell creation and review; ability to collaborate with programming teams

Requirements:

  • Program and validate complex primary efficacy datasets and associated tables, listings, figures, and program statistical analysis tables per the SAP
  • Liaise with clients to propose alternatives or additional analyses, and advise on complex analyses and endpoints to ensure consistency across the clinical trial program
  • Develop and validate macros for statistical analyses and figures; perform stage 3 QC; contribute to SAP text, templates, and standard SAPs
  • Create, validate and QC efficacy dataset specifications for single studies, ISS/ISEs; write ISS/ISE SAPs, DSMB SAPs and Charters; and develop project- or therapeutic-area level documentation

Job description

Overview:

As a Senior/Principal Statistician you’ll work on clinical trials; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Producing and reviewing Statistical Analysis Plans (SAPs), protocols and other pertinent study documentation. You will be a key contributor within our Internal Statistics function and will join at Senior or Principal level, depending on experience.

 

This role is full time, permanent and will be fully remote.

 

Please note that due to internal restrictions the successful candidate must be located in one of the following US States: Massachusetts, New Jersey, New York, Pennsylvania, North Carolina, Texas or California.

Responsibilities:
  • Program and validate complex primary efficacy datasets
  • Program and validate complex summary tables, listings and figures, program statistical analysis tables, according to the SAP
  • Liaise with clients to propose alternatives or additional analyses if needed
  • Develop and validate macros for statistical analyses and figures
  • Perform stage 3 QC
  • Advise on complex analyses and endpoints; ensure consistency across clinical trial program
  • Create, validate and QC of efficacy dataset specifications for single studies, ISS/ISEs, etc.
  • Write ISS/ISE SAPs; DSMB SAPs and Charters
  • Write project level or therapeutic area level documentation
  • Perform QC of SAP text and develop standard SAP text and templates to be used within the company
  • SAP/shell creation and review
Qualifications:
  • Educated to PhD or MSc in Biostatistics/Statistics or a closely related field
  • Extensive CDISC experience (SDTMs and ADaMs)
  • Proficient in SAS, R experience is advantageous also
  • Previous experience working as a Lead Statistician
  • Previous experience with SAP/shell creation and review
  • Previous experience working with a Programming team – reviewing dataset specifications and outputs
  • Ability to work independently and collaboratively in a fast-paced environment

 

Why Join Us

  • Remote working and flexible working hours
  • Career development, mentorship, and continuous learning
  • Supportive, friendly, and collaborative culture
  • Making a Positive Impact: As a B-Corp™ organization, we are committed to sustainability, solid responsibility and strong ethical governance through our ESG initiatives


About Phastar

 

Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment.

We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life-changing therapies to patients faster.

 

 

Awards & Recognition

  • SCRIP – Best Contract Research Organization, Specialist Provider
  • Citeline – 2025 Award Winner
  • Fierce CRO Awards – Recognized Industry Leader

 

Apply Now

 

Be part of a team known for technical expertise, quality, and impact. We value Excellence, Collaboration, Integrity, Innovation, and Passion—and we seek team members who embody these qualities. Apply today!

 

Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.

 

Important notice to Employment businesses/Agencies

 

Phastar does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Phastar's Head of Talent Acquisition to obtain prior written authorization before referring any candidates to Phastar. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Phastar. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Phastar. Phastar shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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