Job Summary:
- Provide statistical support for Phase I–IV clinical trials.
- Participate in protocol development, study design.
- Collaborate with cross-functional teams.
Key Responsibilities:
- Prepare Statistical Analysis Plans (SAPs).
- Perform statistical analyses and interpret study results.
- Support regulatory submissions.
Required Qualifications:
- Master’s or PhD in Statistics, Biostatistics, or related field.
- Experience with SAS and/or R programming.
- Excellent communication and problem-solving skills.
About ClinChoice:
- Global full-service CRO.
- Specializing in clinical development for pharmaceutical companies.
- Over 4,000 professionals in more than 20 countries.
ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries with a mission to contribute to a healthier and safer world.