全职 Statistician 工作, 薪水, OPIS S.r.l. 台灣 公司招聘中 - Ricebowl

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:

• Lead statistical input into clinical study design and analysis
• Develop SAPs, sample size calculations, and randomization schemes
• Deliver high-quality statistical outputs (TFLs) using SAS
• 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

What You Bring:

• Degree in Statistics / Biostatistics (or similar)
• 2+ years of working experience in CRO, pharma, biotech, or research
• Solid knowledge of clinical trials, GCP, and statistical methods
• Working experience with SAS
• Strong communication skills and a proactive mindset
• Fluent English and Taiwanese/Taigi

What we offer:

• Competitive salary
• 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 OPIS, you’ll join a collaborative international team where initiative and growth are encouraged. If you’re ready to build your career in business development within the clinical research industry - we'd love to hear from you!

Who we are:
OPIS 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.
OPIS extensive expertise covers all phases of drug-related 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 all over the world, OPIS 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.

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