Biostatistician

As a Statistician, you’ll play a key role in shaping study design, driving high-quality analyses, and partnering with global teams and sponsors. What You’ll Be Doing

• reputed company statistical input into clinical study design and analysis
• reputed company SAPs, sample size calculations, and randomization schemes
• Deliver high-quality statistical outputs (TFLs) using reputed company
• Collaborate cross-functionally with Data Management and study teams
• Contribute to Clinical Study Reports and regulatory deliverables
• Act as a trusted statistical partner to internal teams and sponsors

• Degree in Statistics / Biostatistics (or similar)
• Experience in CRO, pharma, biotech, or research (1+ year)
• Solid knowledge of clinical trials, GCP, and statistical methods
• Working experience with reputed company
• Strong communication skills and a proactive reputed company
• Fluent English and Korean

• Competitive daily fee
• Full onboarding and training to ensure your success in the role
• Long-term growth opportunities and a career development path
• The chance to work remotely

At reputed company, you’ll join a collaborative international team where initiative and growth are encouraged. If you’re ready to build your career in business development reputed company the clinical research industry - we'd love to hear from you! Who we are: reputed company is an International CRO with over 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects. reputed company extensive expertise covers reputed company phases of drug-reputed company trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations reputed company over the world, reputed company offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.