Senior Biostatistician

Biostatistician, epidemiological , SAS and R.
Full Time, Fulltime
Depends On Experience
Telecommuting not available Travel not required

Job Description

Founded in 1998, Matrix Technology Group is an ERP and IT consulting services provider.

Matrix Technology Group provides Services into ERP, BI and Application Development. Our staff's Passion, and dedication set us a apart from other IT firms. Our team is Dynamic and is focused to our Client needs. Our Team is geared to work with Consultants and our Clients to achieve higher performance. We want to work with you and want to welcome Candidates who are Talented, Passionate, and Dedicated and have Ambition to grow.

One of our highly esteemed client has immediate need for strong Senior Biostatistician

Job Description is as follows:

One of our client is looking for Senior Biostatistician ((Feel Free to reach me at 908-279-1275 OR E-mail me: ssawant at rate

Job Title: Senior Biostatistician 

Location: South San Francisco, CA

Job Description:

 The Senior Biostatistician provides statistical leadership for Actelion US medical affair initiatives. This individual is responsible for all biostatistical aspects of the projects and/or trials and participates in the development and implementation of U.S. Medical Affairs strategies, design, analysis and publication of results of Medical Affairs studies.

 Job Responsibilities

  • Primary responsibilities include the following. Other duties may be assigned.
  • Coordinates and provides statistical representation for all Medical Affairs studies
  • Participates protocol and CRF development with other clinical team/clinical trial team including study design, analysis plan, and reporting.
  • Supports analysis of Medical Affairs studies and associated publications.
  • Ensures statistical design is compatible with the trial objectives.
  • Develops statistical analysis plan.
  • Provides quality assurance on data and all statistical deliverables.
  • Performs statistical analysis.
  • Writes or supports the writing of the statistical section/module of study reports and publications.
  • Serves critically reviews for abstracts, posters and publications.
  • Verifies adherence to statistical standards and SOPs within the project.
  • Supports and leads continuous development and improvement of statistics and programming processes.
  • Provides statistical oversight for projects utilizing contract research organizations (CROs).
  • Support for development of statistical standards and SOPs.
  • Provides resource plans and timelines for deliverables for assigned projects.
  • Serves as statistical resource to other functions. Provides statistical education.
  • Collaborates and communicates effectively with Global Medical, Life Cycle Team and other relevant teams in relation to assigned responsibilities and projects.

 Candidate Qualifications & Requirements

This job requires a combination of analytical, organizational and interpersonal skills. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.


  • Master's or Ph.D. in mathematics, statistics, biostatistics, or related disciplines with 10 years relevant experience.
  • Preferred
  • Sound knowledge of applied statistics, including survival analysis and epidemiological methods.
  • Experience working on post-marketing studies.
  • Experience in supporting congress presentations and publishing in peer-reviewed clinical journals.
  • Experience in coordinating statistical support for a multifaceted project, including managing outsourced statistical services.
  • Professional demeanor with proficient written and oral communication skills; ability to engage effectively throughout all levels of the organization and externally with key opinion leaders.
  • Strong statistical analysis skills in SAS and R.
  • Able to work effectively in a multi-disciplinary team.
  • Knowledge of international clinical research regulations and requirements.
  • Ability to work efficiently in an international team environment.
  • Excellent interpersonal and communication and management/coaching skills.
  • Must be able to work according to timelines and achieve project deadlines.

  ((Feel Free to reach me at 908-279-1275 OR E-Mail me:  ssawant at rate

We are an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristic protected by law.

Dice Id : mategr
Position Id : Sk09-56315
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