Job Duties:
- Contribute to design of early/late-stage protocols across multiple therapeutic areas
- Help draft protocols or amendments
- Attendance and statistical contributions at study team meetings are expected.
Qualification and Required Skills:
- MS or PhD in Statistics or Biostatistics
- Hands-on Phase I/II/III clinical trial experience and proficient in SAS programming
- Excellent oral and written communication skills.
About ClinChoice:
- Global full-service CRO specializing in clinical development
- Over 28 years of proven high-quality delivery and results across all our services
- Our employees are the most valuable company asset
ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, they focus on quality, professional development, and a supportive culture.