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Senior Biostatistician

3-5 years
Preferred by Comapny
11 Nov. 25, 2024
Job Description
Job Type: Full Time Education: A Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline. 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

Job Description: Experienced Biostatistician

As a seasoned Biostatistician, you will take a leadership role in research design and analytical strategies, offering expertise to guide projects from inception to completion. You will contribute to protocol development, statistical analysis plans, and the preparation of high-quality reports, abstracts, and manuscripts. This role emphasizes quality control, collaboration, and mentorship, ensuring that statistical deliverables meet the highest standards. Acting as a functional lead within study teams, you will be accountable for directing Biostatistical activities and providing client-facing solutions that influence study outcomes.


Key Responsibilities

  1. Strategic Leadership:

    • Lead research design and analytical strategies, providing expert advice throughout the project lifecycle.
    • Serve as the functional lead for Biostatistical activities on assigned studies, ensuring quality deliverables.
  2. Statistical Analysis:

    • Develop and execute complex analysis strategies using efficient programming techniques in SAS and R.
    • Perform detailed statistical analyses and contribute to statistical reports, including integrated clinical reports.
  3. Documentation and Reporting:

    • Author or co-author statistical sections of reports, abstracts, and manuscripts.
    • Provide input into statistical analysis plans and ensure they align with study objectives and regulatory standards.
  4. Quality Assurance:

    • Oversee quality control for analysis datasets and deliverables, ensuring compliance with statistical and clinical trial standards.
  5. Collaboration and Client Engagement:

    • Act as a client-facing representative, offering statistical insights and serving as a proactive advisor during study discussions and proposals.
    • Work collaboratively with cross-functional teams to achieve study goals.
  6. Mentorship and Development:

    • Coach and mentor junior biostatisticians, fostering a culture of continuous learning and development.
    • Share knowledge to uplift team capabilities and ensure consistency in statistical approaches.

Qualifications and Skills

Experience:

  • Minimum 5 years of industry experience in statistical analysis related to clinical trials or observational studies.
  • Thorough understanding of statistical aspects in clinical trials or epidemiological studies.

Technical Skills:

  • Proficiency in SAS or R programming.
  • Experience in developing and executing statistical strategies for complex datasets.

Education:

  • Master’s or Ph.D. in BiostatisticsStatisticsMathematics, or a related discipline.

Soft Skills:

  • Strong leadership and team management skills.
  • Excellent oral and written communication skills in English.
  • Confidence, self-reliance, and a quick learner who thrives in a matrix team environment.
  • A strong work ethic and commitment to advancing life-changing treatments for patients.

Additional Requirements:

  • Willingness to travel occasionally as needed for client meetings or team collaboration.

Join Parexel and become a key player in shaping clinical research outcomes. This role offers the opportunity to leverage your expertise, contribute meaningfully to innovative treatments, and mentor the next generation of statistical professionals.