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As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
Job Responsibility:
Provide expert input on the design of clinical development programs
Identify evidence gaps, possible data sources, and design and implement robust evidence-generation plans
Ensure Access/HTA evidentiary activities are strategically aligned
Plan and conduct statistical analyses of clinical trials and other relevant data sources
Interpret and communicate the findings of analyses
Lead or contribute to cross-functional teams
Keep up to date with the changing Access/HTA landscape
Preparing network meta-analysis protocols
Reviewing data extracted from systematic literature reviews
Conducting feasibility assessments
Generating network diagrams
Critically assessing study heterogeneity
Conducting network meta-analysis
Assisting with interpretation and dissemination of findings
Support thought leadership and innovation objectives in advanced analytics
Requirements:
Master's or Doctoral-level degree in applied statistics, health economics, or related quantitative fields
Minimum of 3 years of hands-on experience in the pharmaceutical industry, consultancy, Access/HTA/reimbursement agency, or academic institution
In-depth knowledge of Access and HTA, clinical research and development methods, and international payer evidence requirements
Skilled in research design and statistical methods, such as Generalized Linear Models, Survival Analysis, Network Meta-Analysis, and Bayesian statistics
Proficient in R and GitLab
Strong strategic, collaboration, and communication skills
excellent organization, planning, and prioritization abilities
ability to meet tight deadlines
strong written and verbal communication skills in English
Nice to have:
Pharma affiliate experience is a plus
Experience with SAS, Python, WinBUGS, JAGS, or other relevant statistical software is a plus
What we offer:
Flexibility of working remotely
Supportive and dynamic team
Collaboration, innovation, and continuous learning
Exposure to various product types and therapeutic areas
Development of skills through challenging assignments and mentorship