We are looking for a Biostatistician to join our team!

The Biostatistician is a core member of the Biostatistics & Statistical Programming group who is able to provide sound statistical support for the reporting of both academic and regulatory directed initiatives.

 In this position you will:

  • Support project teams in study design and statistical analysis as well as communicate and interact with project team members and clients
  • Provide statistical input on clinical electronic data capture (EDC) design and edit checks
  • Provide statistical input for the design, writing and review of study protocols, including the design of studies and sample size/power estimations and the development and review of statistical analysis plans (SAPs)
  • Utilize SAS for programming for validation, analysis, and reporting of clinical data (proficiency in other statistical or programming languages e.g. R, Python is welcome)
  • Analyze data for, and prepare and review interim study reports, manuscripts, abstracts, and grants
  • Ensure compliance with GCP, FDA, and ICH guidelines and CPC standards
  • Effectively communicate statistical issues to project team members

Here’s what you will need to bring to the table:

  • Master’s or Ph.D. degree in biostatistics or related field
  • Minimum of 2 years of experience in the analysis of data for clinical trials
  • Ability to work successfully with minimal supervision
  • Demonstrated teamwork skills as you will work closely with others in the development or validation of statistical programming
  • Demonstrable programming experience with SAS 9.0 or higher in a Windows environment
  • Experience with MS Office Suite (Word, Excel, PowerPoint, Outlook)
  • Good knowledge of ICH guidelines, experience with Phase I-III clinical trials and FDA/NDA submissions
  • Impeccable attention to detail
  • Excellent analytical, organizational, and communication skills
  • Demonstrated leadership ability
  • Specific areas of technical expertise are a plus, such as the generation of randomization schedules and/or served as a project unblinded statistician for conduct of analysis for external committees such as Data Monitoring Committees, experience with study design methodology such as adaptive design or pragmatic clinical trials or experience analyzing big data.

Note: Viable applicants will be required to demonstrate their computer skills as well as pass a background check.

This is an in-house position and as such requires the employee to spend about 90% of time in the office vs. working remotely.

At this time CPC is not able to provide relocation assistance to out-of-state candidates.

Please include a short cover letter with answers to the following questions:

  • Why would you be a good candidate for this position?
  • How many years of experience in the analysis of data for clinical trials do you have?
  • Any gaps in your employment history? Please explain.
  • What are your salary expectations?
  • Do you have a Master’s or Ph.D. degree in biostatistics or related field?
  • Are you authorized to work in the United States?
  • Do you now or will you in the future require sponsorship for employment visa status (e.g., H-1B visa status)?

About CPC:

CPC is an academically led clinical 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 25 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’s proprietary database contains more than 1000 clinical investigators located throughout the world.

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. http://www.cpccommunityhealth.org/

CPC offers a comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)

An Equal Opportunity Employer

CPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, national origin, gender, gender identity, veteran status, marital status, sexual orientation, age, disability, genetic information or any other status protected by applicable federal, 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.