Biostatistician at Piper Companies
Remote, Oregon, USA -
Full Time


Start Date

Immediate

Expiry Date

02 Nov, 25

Salary

45.0

Posted On

03 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Trials, Statistical Software, Immunology, Sas, Statistics, Drug Development, Biostatistics, Regulatory Submissions

Industry

Pharmaceuticals

Description

Piper Companies is seeking a remote Biostatistician for a pharmaceutical services leader. The Biostatistician will be responsible designing and analyzing clinical trials, collaborating with cross-functional teams to support drug development and regulatory submissions, and applying advanced statistical methods to ensure high-quality, data-driven decision-making in a fast-paced biotech environment. This role is remote and prefers the candidate to sit on the east coast.

Responsibilities of the Biostatistician:

  • Design and analyze clinical trials and contribute to the clinical development plan of a compound/program.
  • Collaborate with cross-functional teams and stakeholders to deliver statistical components for clinical trials and regulatory submissions.
  • Ensure statistical processes align with company guidelines and regulatory standards.
  • Lead and monitor statistical activities across multiple clinical trials.
  • Communicate complex statistical concepts clearly to both technical and non-technical audiences.

Qualifications for the Biostatistician:

  • 5+ years of relevant experience.
  • Strong expertise in biostatistics and its application in drug development and clinical trials.
  • Proficiency in statistical software such as SAS and/or R.
  • Experience with regulatory submissions and knowledge of eCRT and Define standards.
  • Demonstrated leadership in managing cross-functional teams and statistical deliverables.
  • Preferably experienced in Immunology and familiar with modern statistical models and design approaches.
  • Masters or PhD. in Statistics or related field.
Responsibilities
  • Design and analyze clinical trials and contribute to the clinical development plan of a compound/program.
  • Collaborate with cross-functional teams and stakeholders to deliver statistical components for clinical trials and regulatory submissions.
  • Ensure statistical processes align with company guidelines and regulatory standards.
  • Lead and monitor statistical activities across multiple clinical trials.
  • Communicate complex statistical concepts clearly to both technical and non-technical audiences
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