Senior Statistical Advisor

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🔥 0 minutes ago

🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Innovaderm Research Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

💊 Pharmaceuticals

🏥 Healthcare

💼 Consulting

Pharmaceuticals • Healthcare • Consulting

Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.

📋 Description

• Provide statistical input into Phase I–IV clinical trial development • Assist in protocol development • Manage and support customer relationships • Support statistical requirements for regulatory submissions • Support data analysis and interpretation • Support research and development • Conduct activities in conformance with applicable regulatory requirements, industry guidelines, and Innovaderm standard operating procedures • Respect sponsor requirements and timelines

🎯 Requirements

• Provide statistical input into protocols, including trial design, sample size estimation, power calculations, randomization, and statistical methods • Communicate with clients regarding study protocol or statistical analysis issues • Review statistical analysis plans • Review clinical trial data results, validate statistical output, accurately interpret results, and communicate statistical results and concepts clearly to non-statisticians • Provide support to scientific writers working on Clinical Study Reports • Advise on the design of valid, efficient, and cost-effective clinical trials and other research projects • Provide input into statistical standard operating procedures and general standardization efforts • Collaborate effectively with clinical trial implementation teams • Keep abreast of new developments in statistics, drug development, and regulatory guidance through literature review • Required experience, qualifications, and/or adequate training for other assigned responsibilities • Work permit for Canada required

🏖️ Benefits

• Flexible work schedule • Permanent full-time position • Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities) • Ongoing learning and development • Attractive advancement opportunities