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Overview

Company
CPC Clinical Research
Location
all cities, TX 44
Employment type
On-site
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  • Commissions Specialist (44)
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  • Senior Product Designer, Creators (44)
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C
CPC Clinical ResearchVerified Employer

Business Services & Consulting • all cities, TX 44

Senior Biostatistician (44)

all cities, TX 44On-sitePosted 5 hours ago
Business Services & Consulting

About the Role

Job Title

Leadership & Project Oversight

Study Design & Statistical Strategy

Data Management & Systems Collaboration

Statistical Programming & Analysis

Reporting & Scientific Communication

Regulatory Compliance & Quality Assurance

Collaboration &Stakeholder Engagement

Specialized & Strategic Contributions

Qualifications

Required

  • PhD or Master's degree in Biostatistics, Statistics, or related field with at least 5 years of experience in clinical trial data analysis
  • Demonstrated programming proficiency in SAS (version 9.0 or higher)
  • Experience supporting Phase I–III clinical trials
  • Strong knowledge of ICH guidelines and regulatory requirements; familiarity with FDA submission processes
  • Familiarity with CDISC standards (e.g., SDTM, ADaM) for regulatory submissions
  • Proven leadership experience managing projects and mentoring team members
  • Proficiency with Microsoft Office tools (Word, Excel, PowerPoint)
  • Experience working on integrated summaries of safety and efficacy (ISS/ISE) or similar large-scale reporting efforts
  • Strong analytical, organizational, and problem-solving skills with high attention to detail
  • Excellent communication and interpersonal skills, with the ability to convey complex statistical concepts clearly
  • Ability to manage multiple trials and priorities simultaneously with minimal disruption to productivity

Preferred

  • Experience with FDA/NDA submissions and regulatory interactions
  • Experience working in a client-facing or CRO environment
  • Therapeutic area expertise
  • Proficiency in R, Python, or other advanced analytical tools
  • Track record of contributions to publications, abstracts, or conference presentations

About CPC

CPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 30 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more.

CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.

CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy.

CPC offers:

  • Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
  • Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)
  • 11 paid holidays
  • 15 - 25 vacation days based on years of service
  • Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours)
  • Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)
  • Flexible and remote work schedules

An Equal Opportunity Employer

CPC is dedicated to the principles of equal employment opportunity (EEO).CPC prohibits unlawful discrimination against applicants or employees on the basis of age 40 and over, race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, sexual orientation, gender identity, gender expression, color, religion, creed, national origin, ancestry, disability, military status, genetic information, marital status, or any other status protected by applicable state or local law.

It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.

Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at careers@cpcmed.org.

Job Title

Leadership & Project Oversight

Study Design & Statistical Strategy

Data Management & Systems Collaboration

Statistical Programming & Analysis

Reporting & Scientific Communication

Regulatory Compliance & Quality Assurance

Collaboration &Stakeholder Engagement

Specialized & Strategic Contributions

Qualifications

Required

  • PhD or Master's degree in Biostatistics, Statistics, or related field with at least 5 years of experience in clinical trial data analysis
  • Demonstrated programming proficiency in SAS (version 9.0 or higher)
  • Experience supporting Phase I–III clinical trials
  • Strong knowledge of ICH guidelines and regulatory requirements; familiarity with FDA submission processes
  • Familiarity with CDISC standards (e.g., SDTM, ADaM) for regulatory submissions
  • Proven leadership experience managing projects and mentoring team members
  • Proficiency with Microsoft Office tools (Word, Excel, PowerPoint)
  • Experience working on integrated summaries of safety and efficacy (ISS/ISE) or similar large-scale reporting efforts
  • Strong analytical, organizational, and problem-solving skills with high attention to detail
  • Excellent communication and interpersonal skills, with the ability to convey complex statistical concepts clearly
  • Ability to manage multiple trials and priorities simultaneously with minimal disruption to productivity

Preferred

  • Experience with FDA/NDA submissions and regulatory interactions
  • Experience working in a client-facing or CRO environment
  • Therapeutic area expertise
  • Proficiency in R, Python, or other advanced analytical tools
  • Track record of contributions to publications, abstracts, or conference presentations

About CPC

CPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 30 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more.

CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.

CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy.

CPC offers:

  • Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
  • Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)
  • 11 paid holidays
  • 15 - 25 vacation days based on years of service
  • Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours)
  • Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)
  • Flexible and remote work schedules

An Equal Opportunity Employer

CPC is dedicated to the principles of equal employment opportunity (EEO).CPC prohibits unlawful discrimination against applicants or employees on the basis of age 40 and over, race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, sexual orientation, gender identity, gender expression, color, religion, creed, national origin, ancestry, disability, military status, genetic information, marital status, or any other status protected by applicable state or local law.

It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.

Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at careers@cpcmed.org.

What You'll Do

PhD or Master's degree in Biostatistics, Statistics, or related field with at least 5 years of experience in clinical trial data analysis
Demonstrated programming proficiency in SAS (version 9.0 or higher)
Experience supporting Phase I–III clinical trials
Strong knowledge of ICH guidelines and regulatory requirements; familiarity with FDA submission processes
Familiarity with CDISC standards (e.g., SDTM, ADaM) for regulatory submissions
Proven leadership experience managing projects and mentoring team members

Skills & Technologies

Business Services & Consulting

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