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
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.
Skills Required
- Degree in Statistics, Biostatistics, or a similar field
- At least 2 years of work experience in a CRO, pharmaceutical, biotechnology, or research environment
- Knowledge of clinical trials, GCP, and statistical methods
- Working experience with SAS
- Strong communication skills and a proactive mindset
- Fluency in English and Taiwanese/Taigi
What We Do
OPIS was founded in 1998 by medical doctors from the Pharma Industry and is a Global clinical CRO with 25 years of experience in a wide range of therapeutic areas. OPIS provides full-service, 360° clinical trial support from study concept creation and protocol development to full project execution, study data handling and up to study closure, analysis, and reporting. We manage Phase I-IV, interventional, non-interventional and medical devices studies on an international level. In addition, OPIS also manages pre- and post-marketing clinical investigations for medical and diagnostic devices, nutraceutical, and food supplement studies. Our qualified, fully trained, and dedicated staff has managed 1470 studies to date. OPIS’s strength lies in its people and its specialized teams who assist clients from A-Z with medical writing, scientific and statistical consultancy for trial design and skilled teams of operational staff that ensure high quality project execution, with global coverage. Our mission is to increase the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system... etc. OPIS is committed to continuous growth and expansion, while currently we have affiliates in 17 countries around the world. For more information, visit www.opisresearch.com
