Therapeuticsinc

Therapeuticsinc

Sr. Biostatistician

San Diego, California, United States · Senior

Sponsorship not specified$115k-$140kDetected 33 days ago
StatisticsProject ManagementForecastingClinical TrialsClinical ResearchFDA RegulatorySASResearchLeadershipCommunicationCollaborationProblem SolvingAdaptabilityBiostatistics

About the role

  • Recognized as one of San Diego's Top Workplaces, we have built a culture that values collaboration, diverse perspectives, continuous learning, and mutual respect.
  • We believe that great ideas come from talented individuals who are empowered to contribute, grow, and make a meaningful impact.

Requirements

  • As the only full-service dermatology-focused CRO, we combine deep therapeutic expertise with a commitment to delivering exceptional results for our clients and their patients.
  • Your ideas, expertise, and contributions are valued, and the work you do has a direct impact on our colleagues, clients, and the patients we ultimately serve.
  • You are someone who takes pride in doing exceptional work and believes that great organizations are built by great people.
  • At the same time, you are resourceful, adaptable, and confident in your ability to think critically, solve problems, and move initiatives forward independently when needed.

Compensation

  • You should have a Master's or Doctoral level degree in statistics with at least 5 years of experience performing statistical analysis and reporting for clinical trials.
  • You should have a thorough understanding of the requirements of the management and analysis of clinical data as required by GCPs, FDA and ICH guidelines is essential.
  • You should possess excellent problem solving, organizational, written and oral communication skills, the ability to manage multiple priorities and attention to detail is critical.
  • You should have strong computer proficiency and SAS programming skills including experience implementing CDISC standards end-to-end are required.
  • You will have the ability to perform statistical analyses of clinical data, prepare written interpretations of statistical results and to integrate these findings into clinical study reports and publications.
  • You will have knowledge of core technical and regulatory requirements.
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