Senior/Principal Biostatistician

Posted 5 Days Ago
Be an Early Applicant
Remote
7+ Years Experience
Healthtech • Pharmaceutical
The Role
The Senior/Principal Biostatistician will provide statistical support for all phases of clinical development, lead projects, mentor junior team members, and interact with sponsors. Responsibilities include developing SAS programs, authoring statistical analysis plans, and validating analysis datasets. The role requires a Master's degree or PhD in Statistics or related field with 7-10 years of experience in Biostatistics for a Clinical Research Organisation.
Summary Generated by Built In

Precision for Medicine are recruiting an experienced Senior Biostatistician/Principal Biostatistician to work remotely in UK, Spain, Poland, Hungary, Serbia, Romania or Slovakia.

Position Summary:

To provide statistical support for all phases of clinical development. Specific responsibilities include reviewing statistical sections of protocols, writing statistical analysis plans, and developing SAS programs for tables, listings, figures and analysis datasets in accordance with Precision and/or sponsor procedures or study specific guidelines.

For this level, the role will include project work as a Lead Biostatistician, and additionally mentoring and supporting more junior team members.

Essential functions of the job include but are not limited to:

  • Generate randomization schedules
  • Assist with statistical methods review of the clinical study protocol.
  • Provide and/or verify sample size calculations
  • Provide input into development of case report forms (CRFs)
  • Author statistical analysis plans, including development of table, figure and listing shells
  • Validate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS
  • Assist with quality control for statistical based SAS programs and other study documents (e.g., presentations and reports)
  • Provide statistical support for supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
  • Assist with statistical consulting tasks
  • Review output across programs to ensure consistency
  • Provide statistical analysis and reports to Data Monitoring Committees (DMCs) as the unblinded statistician
  • Review statistical sections of clinical study reports
  • Work directly with sponsors, project managers, and external vendors on statistics-related project components
  • Interact directly with study team
  • Interact directly with sponsors
  • Assist with completion of statistical activities for study within timelines
  • Provide units for development of monthly project invoices
  • Train and mentor new biostatisticians
  • Assist with bid defense meetings
  • Additional responsibilities for Senior and Principal levels, as senior team members

 Qualifications:

Minimum Required:

  • Master's degree / PhD or equivalent in Statistics, Biostatistics, or related field with strong relevant experience
  • At least 7 to 10 years experience working as a Biostatistician for a Clinical Research Organisation

Other Required:

  • Demonstrates extensive knowledge with industry standards, such as the ICH guidelines, 21 CFR Part 11, and FDA guidelines
  • Experience with SAS
  • Familiarity with complex statistical methods that apply to Phase I-IV clinical trials

Preferred:

  • Experience with Oncology desirable
  • Knowledge and experience of CDISC data structures

Skills:

  • Understanding of advanced clinical trial design concepts, such as non-inferiority, adaptive methods, type-I error protection, dynamic randomization, and sample size estimation in complex settings
  • Understanding of advanced statistical methodologies applicable to clinical trials, such as survival analysis, stratified or covariate analyses, sequential methods, and strategies for handling missing data
  • Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines
  • Excellent communication and interpersonal skills to effectively interface with others
  • Excellent problem solving skills
  • Excellent presentation skills

Competencies:

  • Sound judgment/decision making
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Service oriented, accountable and flexible
  • Fluent in written and spoken English
  • Follow applicable regulations, including FDA, ICH, and Precision Policies and Procedures
  • At all times to promote the image of Precision, acting as an ambassador to the Company
  • Ensure that all internal systems are routinely updated as appropriate (e.g., timesheets, expense reports, financial reports, etc.)

#LI-NC1 #LI-Remote

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Top Skills

SAS
The Company
HQ: Bethseda, MD
396 Employees
On-site Workplace
Year Founded: 2012

What We Do

We founded Precision Medicine Group in 2012 because we believed there was a transformational opportunity to improve the process of bringing new drugs to market. It involves utilizing technology, data, and human expertise. It is a big challenge that requires diverse talents. Our model involves both nurturing and investing organically and acquiring capabilities that we do not have but critically need. Our core executive team is anchored to this model, building life science services that address fundamental changes in healthcare that are necessary for health and outcomes improvement.

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