Sr. Biostatistician

Redbock - an NES Fircroft company; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

An established industry player in biotechnology is seeking a Senior Biostatistician to join their dynamic team. This role offers the chance to engage in hands-on exploratory analysis while supporting both medical affairs and traditional clinical trials. You will work closely with programmers to produce essential analyses for clinical studies, leveraging your expertise in SAS and innovative statistical methodologies. If you are passionate about advancing your career in a supportive environment and making a meaningful impact in the life sciences, this opportunity is perfect for you.

Benefits

Medical insurance

Vision insurance

401(k)

Disability insurance

Qualifications

• 5+ years of Biostatistics experience in the life science industry.
• Strong SAS experience with TLF development and expertise.

Responsibilities

• Provide hands-on statistical support to the Biostatistics team.
• Conduct analyses and propose new statistical methodologies.
• Collaborate with cross-functional teams for statistical data analysis.

Skills

SAS

Statistical Analysis

Clinical Trials

Exploratory Analysis

Cross-functional Collaboration

Education

MS degree in Biostatistics

Tools

SAS

Job description

Direct message the job poster from Redbock - an NES Fircroft company

Principal Recruitment Consultant – Helping professionals grow their careers, while identifying top subject matter experts for clients.

SENIOR BIOSTATISTICIAN – (1 OPENING)

12+ MONTHS RENEWABLE

SUMMARY:

A biotechnology leader on the east coast needs a Senior Biostatistician consultant to support their team on a long-term basis. This is an exciting opportunity to be part of a strong FSP team for our client’s multiple programs.

This consultant will be responsible for performing hands-on exploratory analysis. Their efforts will be split 50/50 between analysis of previous clinical trials (Medical Affairs) and traditional clinical trials work. They must be comfortable working hands-on, partnering with the programmers to produce analysis either needed for the clinical studies per the SAP or as per the discussions with the medical affairs.

DUTIES & RESPONSIBILITIES:

1. Independently provide detailed, hands-on statistical support to the Biostatistics team
2. Independently conduct analyses suggested by the data; propose new/novel statistical methodological approaches to improve the efficiency and sensitivity of study results.
3. Review SAS summaries and perform analysis
4. Oversee TFL development (tables, listings, figures)
5. Perform exploratory analysis
6. Understand production and QC of analysis
7. Work collaboratively with cross-functional teams to meet study/product deliverables and timelines for statistical data analysis and reporting.

QUALIFICATIONS & REQUIREMENTS:

1. Minimum of MS degree in Biostatistics and at least 5+ years of Biostatistics experience within the life science industry, preferably on the Sponsor side
2. Experience supporting analysis of previously clinical trials for Medical Affairs
3. Experience supporting traditional clinical trials work for ongoing studies; shells, statistical QC, review of outputs, dry runs, etc.
4. Must have strong SAS experience, TLF development and expertise
5. Experience supporting regulatory submissions and submissions requirements
6. Understanding of the drug development process and clinical trials

LOCATION:

Work will be performed remotely. Eastern time zone must be accommodated.

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Consulting

Industries

Pharmaceutical Manufacturing