Biostatistician

Posted 4 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
Mid level
Pharmaceutical
The Role
Conduct statistical analyses for clinical research studies using SAS. Responsibilities include developing statistical analysis plans, generating randomization schedules, preparing tables, figures, listings, and reports, interpreting data, supporting database transmissions, reviewing deliverables, assisting with programming, and coordinating with internal teams and clients.
Summary Generated by Built In
Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

 
 
We are seeking a full-time Biostatistician for our Data Management and Biometric department..  The selected candidates will be responsible for developing statistical analysis plan, performing statistical analyses using SAS and preparing reports for assigned projects.
 

Responsibilities

  • Data analysis and interpretation
  • Provide input on data collection methods and coordinate customized electronic database transmissions to 
    Sponsors 
  • Support the randomization process by generating randomization schedules and randomizations plans
  • Develop statistical analysis plans for simple to complex studies including table shells and, when appropriate, other programming plans
  • Direct and oversee the execution of planned statistical analysis and summarization for simple to complex studies (including tables, figures, and data listings) independently 
  • Write statistical methods and results sections of reports for assigned projects
  • Review draft report for consistency and completeness 
  • Effectively communicate with colleagues and clients regarding timelines, deliverables, and commitments 
  • Provide programming assistance, as applicable  
  • Interact with internal departments (e.g., data management, project management, etc.) 
  • Lead and/or participate in functions required to ensure success of department and/or market segment team
     
     

Requirements

  • Master's degree in Statistics-related field and 3+ years industry experience or the equivalent OR 
    Bachelor's degree in Statistics-related field and 3+ years industry related experience and 4+years SAS 
    programming experience of the equivalent 
  • Proficiency with SAS programming 
  • Ability to organize multiple priorities 
  • Excellent communication and leadership skills 
  • Demonstrated problem solving and decision making skills
  • Excellent interpersonal skills
     

Celerion Values:       Integrity   Trust   Teamwork   Respect
 
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
 

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Skills Required

  • Master's degree in Statistics or a related field with 3 or more years of industry experience, or a bachelor's degree in Statistics or a related field with equivalent industry experience.
  • At least 3 years of industry-related experience.
  • At least 4 years of SAS programming experience for candidates with a bachelor's degree, or equivalent experience.
  • Proficiency with SAS programming.
  • Ability to organize multiple priorities.
  • Excellent communication and leadership skills.
  • Demonstrated problem-solving and decision-making skills.
  • Excellent interpersonal skills.
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The Company
HQ: Lincoln, NE
1,029 Employees
Year Founded: 2010

What We Do

Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines. With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings. Our operations are strategically located in: Lincoln, Nebraska (Corporate Headquarters) Philadelphia, Pennsylvania Phoenix, Arizona Belfast, Northern Ireland,UK Zurich, Switzerland Vienna, Austria Richmond, Virginia Montreal, Quebec, Canada For more information, visit: www.celerion.com

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