Biostatistician - Data Analyst for Healthcare Innovation

6 days ago

Boston, Lincolnshire, United Kingdom Unreal Gigs Full time
Biostatistician Job Description

At Unreal Gigs, we're seeking a skilled Biostatistician to join our team and contribute to the advancement of healthcare through data-driven insights. As a Biostatistician, you will play a crucial role in analyzing and interpreting health data, driving critical decisions in clinical trials, medical research, and healthcare strategy.

Key Responsibilities:
  1. Design and Analyze Clinical Trials:
  • Collaborate with clinical researchers to design statistically sound clinical trials, determining sample sizes, randomization strategies, and statistical analysis plans.
  • Analyze trial data to assess drug efficacy, safety, and outcomes.
Perform Statistical Analysis for Research Studies:
  • Conduct complex statistical analyses for a range of medical and epidemiological studies.
  • Analyze data from observational studies, longitudinal research, and experimental trials, providing insights into trends, associations, and causal relationships.
Develop Statistical Models and Algorithms:
  • Build and refine statistical models that help understand and predict patient outcomes, disease progression, and treatment efficacy.
  • Work with big data, including patient registries, electronic health records, and genetic data, to develop predictive algorithms.
Collaborate on Regulatory Submissions:
  • Support the preparation of regulatory submissions, ensuring that statistical methodologies meet regulatory standards set by agencies like the FDA or EMA.
  • Provide statistical analysis results and interpretations for clinical study reports (CSRs) and regulatory filings.
Ensure Data Quality and Integrity:
  • Develop and implement data validation strategies to ensure the accuracy and reliability of data used in clinical trials and research studies.
  • Conduct data cleaning and manage missing data, ensuring that analyses are based on high-quality data.
Generate Reports and Visualizations:
  • Create detailed reports, data visualizations, and presentations that communicate the results of statistical analyses clearly to both technical and non-technical stakeholders.
  • Ensure that findings are presented in a way that supports decision-making in clinical research and healthcare.
Advise on Study Protocols and Statistical Best Practices:
  • Provide guidance to clinical research teams on statistical best practices, including study design, data collection methods, and appropriate statistical tests.
  • Ensure that research methodologies align with scientific and ethical standards.
Requirements

Required Skills:

  • Biostatistics and Data Analysis Expertise: Strong expertise in biostatistics, with experience applying statistical techniques to clinical trials, medical research, and epidemiological studies.
  • Clinical Trial Design and Analysis: Experience in designing and analyzing clinical trials, including sample size calculations, randomization techniques, and interim analysis.
  • Data Modeling and Statistical Methods: Expertise in developing statistical models and applying methods such as survival analysis, mixed-effects models, and Bayesian analysis.
  • Regulatory Knowledge: Understanding of regulatory standards, including FDA and EMA guidelines, for statistical methodologies in clinical trials.
  • Communication and Collaboration: Excellent collaboration skills with the ability to work with multidisciplinary teams, including clinicians, researchers, and regulatory professionals.

Educational Requirements:

  • Master's or Ph.D. in Biostatistics, Statistics, Epidemiology, or a related field.
  • Certifications or additional coursework in clinical trial design, statistical programming, or healthcare data analysis are a plus.

Experience Requirements:

  • 3+ years of experience in biostatistics, with hands-on experience in analyzing clinical trial data or conducting medical research.
  • Experience working with statistical software such as SAS, R, SPSS, or Python for data analysis and model development.
  • Experience working in regulated environments and supporting regulatory submissions (e.g., FDA, EMA) is highly desirable.

Benefits

  • Health and Wellness: Comprehensive medical, dental, and vision insurance plans with low co-pays and premiums.
  • Paid Time Off: Competitive vacation, sick leave, and 20 paid holidays per year.
  • Work-Life Balance: Flexible work schedules and telecommuting options.
  • Professional Development: Opportunities for training, certification reimbursement, and career advancement programs.
  • Wellness Programs: Access to wellness programs, including gym memberships, health screenings, and mental health resources.
  • Life and Disability Insurance: Life insurance and short-term/long-term disability coverage.
  • Employee Assistance Program (EAP): Confidential counseling and support services for personal and professional challenges.
  • Tuition Reimbursement: Financial assistance for continuing education and professional development.
  • Community Engagement: Opportunities to participate in community service and volunteer activities.
  • Recognition Programs: Employee recognition programs to celebrate achievements and milestones.

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