Instagram
youtube
Facebook

Principal Biostatistician

3+ years
Not Disclosed
10 Nov. 26, 2024
Job Description
Job Type: Full Time Education: MSc./M. Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Senior Biostatistician
Location: Global (Flexible working environment)

Parexel is seeking a Senior Biostatistician to contribute to the design, analysis, and interpretation of clinical trials, playing a key role in ensuring the safety and efficacy of innovative health treatments. As a part of the global Biostatistics team, you will leverage your expertise in statistical methodologies to provide robust evidence supporting clinical development while keeping the patient at the center of every decision.

Key Responsibilities

  • Project Leadership:

    • Lead project teams to deliver high-quality statistical deliverables within timelines and budgets.
    • Act as the primary client contact for statistical and contractual matters.
  • Statistical Analysis:

    • Develop and review Statistical Analysis Plans (SAPs) and ensure the use of advanced statistical methods.
    • Oversee the production and QC of derived datasets, tables, figures, and data listings.
    • Provide data and analysis for Data Monitoring Committees (DMCs) as an independent statistician.
  • Documentation & Reporting:

    • Produce randomization schemes, statistical reports, and statistical sections of clinical study reports.
    • Perform quality control and validation of team deliverables.
  • Collaboration & Communication:

    • Engage with clients to discuss study designs, analysis strategies, and results.
    • Support business development by participating in proposal development, sample size estimation, and bid defense meetings.
  • Mentorship:

    • Support and mentor junior team members to ensure adherence to quality and best practices.

Skills & Competencies

  • Strong analytical and problem-solving skills with attention to detail.
  • Excellent project management and leadership capabilities.
  • Solid understanding of statistical issues in clinical trials.
  • Proficiency in SAS programming and familiarity with other statistical tools is an advantage.
  • Effective communication skills for client interactions, presentations, and reporting.
  • Ability to work independently while fostering collaboration in a matrix environment.
  • Business awareness and proactive contribution to client meetings.

Qualifications & Experience

  • PhD in Statistics or a related discipline with 3+ years of relevant experience OR MS in Statistics with 5+ years of experience.
  • Proven expertise in clinical trial design and analysis methodologies.
  • Familiarity with regulatory guidelines and statistical standards in clinical research.
  • Proficiency in written and spoken English, with additional languages advantageous.

Why Join Parexel?

Parexel fosters a culture of collaboration, innovation, and inclusivity. As part of the Biostatistics group, you will:

  • Work in global cross-functional teams where continuous learning is encouraged.
  • Enjoy a flexible working environment that supports your best performance.
  • Have the opportunity to voice your ideas and impact clinical development.

If you’re passionate about improving patient lives through data-driven insights, Parexel offers the platform for your career growth and contribution to life-changing innovations.

For more information and to apply, visit Parexel Careers.