Principal Biostatistician FSP

Cytel

$120K — $150K *
US-Anywhere
+ 2 other locationsRemote
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in statistics or related discipline (PhD preferred).
  • 5+ years of experience in clinical trials within the Pharmaceutical or Biotechnology sector.
  • Strong background in statistical methods and analytics for effective study support.
  • Proficient in SAS and R programming, with a focus on quality control of statistical outputs.
  • Knowledgeable in ICH guidelines and CDISC standards for regulatory submissions.
  • Experience in leading study activities and collaborating with cross-functional teams.
  • Strong communication skills for explaining complex statistical concepts clearly.

Responsibilities

  • Provide statistical support for clinical studies related to Alzheimer's and Type 2 Diabetes.
  • Participate in the development of study protocols and engage in sample size calculations.
  • Review CRFs and create statistical analysis plans (SAPs) with clear dataset specifications.
  • Conduct statistical analyses and interpret results effectively.
  • Prepare clinical study reports and integrated summaries for submissions.
  • Lead study activities as necessary and ensure results meet deadlines.
  • Effectively communicate methodology and decision impacts using accessible language.

Benefits

  • Opportunity to lead Phase I-III clinical trials in a cutting-edge health domain.
  • Exposure to multidisciplinary collaborations within clinical research teams.
  • Professional growth with the potential for mentorship and innovation.
  • Flexible work environment accommodating shifting priorities.
Full Job Description
Job Description

As Principal Biostatistician, adapt at utilizing advanced statistical methods, you will support or lead one or more Phase I-III clinical studies specially focusing on Alzheimer's and Type 2 Diabetes.

Responsibilities

As a Principal Biostatistician, your responsibilities include:
  • providing statistical support to clinical studies, with a focus on Hypertension;
  • participating in the development of study protocols, including participation in study design discussions and sample size calculations;
  • reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications;
  • performing statistical analyses;
  • interpreting statistical results;
  • preparing clinical study reports, including integrated summaries for submissions;
  • leading study activities when called upon;
  • utilizing your strong communication skills to present and explain methodology and consequences of decisions in lay terms;
  • serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
  • being adaptable and flexible when priorities change


Qualifications

What we're looking for:
  • Master's degree in statistics or a related discipline. PhD strongly desired.
  • 5+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry. Experience working for a CRO strongly desired.
  • Experience in sample size calculation, protocol concept development, protocol development, SAP and preparing clinical study reports including integrated summaries for submissions.
  • Knowledge and implementation of advanced statistical methods.
  • Good SAS and R programming skills for QCing critical outputs, Efficacy/Safety tables and working closely with Programmers. Knowledge of R programming a plus.
  • Strong knowledge of ICH guidelines.
  • Solid understanding & implementation of CDISC requirement for regulatory submissions.
  • Adept in ADaM specifications generation and QC of datasets.
  • Submissions experience.
  • Experience working with cross-functional teams, a Study Management Team (SMT) or similar teams for different clients.
  • Effective communicator: able to explain methodology and consequences of decisions in lay terms.
  • Team player; willingness to go the extra distance to get results, meet deadlines, etc.
  • Ability to be flexible when priorities change and deal with ambiguity.

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