Statistician

TRI

$80K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in biostatistics, statistics, epidemiology, or a related field.
  • 3-5 years of experience in a CRO (Contract Research Organization) environment.
  • Proficient in statistical methods applicable in clinical research.
  • Strong programming skills in SAS and/or R.
  • Ability to handle multiple tasks effectively.
  • Capable of working independently and collaboratively within a team.
  • Excellent verbal and written communication skills for technical concepts.

Responsibilities

  • Collaborate with clinical investigators and cross-functional teams on study design.
  • Work with Medical Writing to develop protocols with statistical input.
  • Create statistical analysis plans and implement analysis programs.
  • Review protocols to ensure adherence to study objectives and standards.
  • Generate treatment allocations for randomized clinical studies.
  • Perform statistical analyses and validate application programs.
  • Develop safety reports and metrics to monitor participant safety.

Benefits

  • Comprehensive health insurance plans.
  • Generous time-off policy.
  • Professional development opportunities both internally and externally.
Full Job Description
Job Title

Statistician

Location

Bethesda, MD 20817 US (Primary)

Category

Information Technology

Job Type

Full-Time

Salary Range

$80,000.00-120,000.00/YEAR

Education

PhD

Travel

None

Job Description

  • Collaborating with clinical investigators, sponsor, and cross-functional teams to determine study design.
  • Collaborating with Medical Writing and Project Management teams on protocol development, including writing sections pertaining to statistical input.
  • Development of statistical analysis plans and programs to perform analyses and display study data.
  • Reviewing protocols and case report forms to ensure that protocol objectives are met and standards are maintained.
  • Generating treatment allocations in randomized clinical research studies and ensuring proper implementation.
  • Performing statistical analyses; writing and validating application programs, including for centralized monitoring purposes.
  • Implementing data and safety monitoring reports to ensure participants' safety.
  • Developing metrics and generating quality control reports to optimize the performance of clinical sites and the coordinating center.
  • Generating study reports to be distributed to internal and external monitoring committees and regulatory bodies.
  • Participating in professional development activities both within and outside the company.
  • Other duties as assigned.


Job Requirements

  • PhD in biostatistics, statistics, epidemiology or related field.
  • Minimum of 3-5 years of experience in a CRO environment
  • Demonstrated proficiency with statistical methods and applications in clinical research.
  • Strong programming skills in SAS and/or R.
  • Ability to manage multiple tasks.
  • Ability to work independently, as well as in a team environment.
  • Ability to effectively communicate technical concepts, both written and oral.


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