Biostatistics Opportunities at Parexel
Department: Biostatistics
About the Team
A career in Biostatistics at Parexel offers the opportunity to contribute to clinical research by applying statistical expertise to the design, analysis, and interpretation of clinical trial data. Biostatisticians work closely with cross-functional teams to support the development of safe and effective therapies while ensuring scientific accuracy and regulatory compliance.
Why Join Parexel?
Work on global clinical trials across multiple therapeutic areas.
Collaborate with experts in Clinical Operations, Data Management, Regulatory Affairs, Medical Writing, and Statistical Programming.
Gain exposure to innovative technologies, AI-enabled solutions, and advanced statistical methodologies.
Benefit from flexible work arrangements, including office-based, home-based, or hybrid options.
Access continuous learning, professional development, mentorship, and internal career growth opportunities.
Be part of a collaborative, patient-focused, and inclusive work environment.
Key Responsibilities (Typical Biostatistics Roles)
Design statistical methodologies for clinical studies.
Develop Statistical Analysis Plans (SAPs).
Perform statistical analyses for clinical trial data.
Review and interpret study results to support clinical and regulatory decisions.
Collaborate with Statistical Programmers, Clinical Data Management, Medical Writers, and Regulatory teams.
Ensure compliance with ICH, GCP, and regulatory guidelines.
Support regulatory submissions with statistical outputs and documentation.
Participate in protocol development and study design discussions.
Provide statistical input for publications, manuscripts, and clinical study reports.
Required Qualifications
Bachelor's, Master's, or Ph.D. in Statistics, Biostatistics, Mathematics, or a related quantitative discipline.
Experience in Biostatistics within the pharmaceutical, biotechnology, CRO, or clinical research industry (experience requirements vary by role).
Strong understanding of clinical trial design and statistical methodologies.
Knowledge of ICH-GCP and regulatory guidelines.
Required Skills
Statistical analysis and interpretation.
Clinical trial design and methodology.
Statistical Analysis Plan (SAP) development.
SAS and/or R programming.
Data analysis and visualization.
Strong analytical and problem-solving skills.
Excellent written and verbal communication.
Cross-functional collaboration and stakeholder management.
Career Growth at Parexel
Parexel offers opportunities to grow through:
Mentorship and leadership development.
Cross-functional project exposure.
Global collaboration with international teams.
Continuous learning and professional training.
Flexible work arrangements supporting work-life balance.
Employee Stories & Insights
Parexel showcases employee experiences across various functions, including:
Yogita Thoke – Senior Biostatistician
Jaeyeon – Regulatory & Access Consultant
Hitarth – Regulatory Affairs Consultant
Sathvika Govind – Senior Regulatory Affairs Associate
Rahul Kamath – Health Economics Consultant
Boris Braylyan – Chief Digital & Data Officer
Catia – Senior Director, Clinical Operations
Mika Pollack – Project Director
Diana Hengartner – Senior Medical Director
These stories highlight career growth, leadership development, innovation, flexible work culture, and Parexel's commitment to advancing clinical research while supporting employee development.
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Atlanta | Augusta | Rome |Maine :
Bangor | Brewer |New Jersey :
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