Warman O'Brien
Lead Biostatistician (Contract)
We’re partnered with a small, innovative clinical‑stage biopharmaceutical company harnessing the power of human genetics to develop novel small molecule precision medicines for patients with renal, metabolic, and cardiovascular diseases.
Clinical-stage Biopharma | Renal, Metabolic & Cardiovascular Diseases | Remote or Local (San Fran -Preferred)
The team is seeking an experienced
Lead Biostatistician (Contract)
to play a visible role supporting late‑stage clinical programs. You’ll collaborate cross‑functionally with clinical, regulatory, and data science teams, providing statistical leadership at the
study
or
compound
level (depending on seniority).
Key Responsibilities
Serve as study or compound lead statistician across multiple clinical trials.
Oversee CROs and vendors to ensure high‑quality statistical deliverables.
Provide statistical input into protocol design, analysis plans, and regulatory submissions.
Interpret and communicate statistical results to cross‑functional stakeholders.
Support strategic decision‑making in clinical development programs.
Requirements
Advanced degree (MS/PhD) in Biostatistics, Statistics, or related field.
Strong hands‑on experience as a lead statistician in clinical development (biotech or pharma).
Solid understanding of regulatory requirements and clinical trial methodology.
Experience with CRO oversight and vendor management.
Details
Type:
Contract (potential to convert to FTE in 2026)
Location:
Remote (local candidates preferred for potential future FTE conversion)
Level:
Open to senior to director‑level, depending on experience
What to do next If this opportunity is of interest, please apply direct or share a copy of your CV to Brook@warmanobrien.com
Contact For confidential discussions about potential opportunities, contact Brook Bridges at +1 617‑546‑7985.
#J-18808-Ljbffr
Clinical-stage Biopharma | Renal, Metabolic & Cardiovascular Diseases | Remote or Local (San Fran -Preferred)
The team is seeking an experienced
Lead Biostatistician (Contract)
to play a visible role supporting late‑stage clinical programs. You’ll collaborate cross‑functionally with clinical, regulatory, and data science teams, providing statistical leadership at the
study
or
compound
level (depending on seniority).
Key Responsibilities
Serve as study or compound lead statistician across multiple clinical trials.
Oversee CROs and vendors to ensure high‑quality statistical deliverables.
Provide statistical input into protocol design, analysis plans, and regulatory submissions.
Interpret and communicate statistical results to cross‑functional stakeholders.
Support strategic decision‑making in clinical development programs.
Requirements
Advanced degree (MS/PhD) in Biostatistics, Statistics, or related field.
Strong hands‑on experience as a lead statistician in clinical development (biotech or pharma).
Solid understanding of regulatory requirements and clinical trial methodology.
Experience with CRO oversight and vendor management.
Details
Type:
Contract (potential to convert to FTE in 2026)
Location:
Remote (local candidates preferred for potential future FTE conversion)
Level:
Open to senior to director‑level, depending on experience
What to do next If this opportunity is of interest, please apply direct or share a copy of your CV to Brook@warmanobrien.com
Contact For confidential discussions about potential opportunities, contact Brook Bridges at +1 617‑546‑7985.
#J-18808-Ljbffr