Life Sciences Statistician

ABOUT COMPANY

Clever Access is a consulting firm for Pharmaceutical and Biotech companies, specialised in strategic advice for Market Access, Pricing and Health Economics and Outcomes Research.

OPPORTUNITY & MAIN RESPONSIBILITIES

Be part of building the next generation toolbox for life sciences organizations

The employee is expected to manage and execute statistical analysis in the context of life sciences research projects across multiple therapeutic areas and diverse geographic markets.

Responsibilities include (but not limited to) the following:

• Analysis of electronic medical records and health insurance data,
• Meta-analysis (from simple to advanced forms),
• Analysis of clinical trial data (patient-level),
• Development of study design and protocol,
• Development of statistical analysis plans (SAPs),
• Statistical programming (in SAS, R, etc.),
• Development of macros,
• Development of review reports, summaries and other project deliverables,
• Prepare and deliver presentations to clients,
• Participate in methodological research projects and author scientific publications.

WE OFFER

• Salary based on experience and skills.
• Participation in interesting and challenging projects in global structures.
• Multicultural, dynamic environment.
• Good working atmosphere.
• Opportunity to build up expertise through coaching and trainings.
• Work in a well-established and international company.
• Retention program associated to personal development plan.

REQUIREMENTS

This position requires a post-graduate degree (Engineer, MSc or PhD) in statistics / biostatistics / epidemiology.

Must have:

• Working knowledge of SAS and/or R programming, 
• Excellent IT literacy e.g. Word, PowerPoint and Excel,
• Fluency in English,
• Team-oriented mind-set,
• Strong analytic capabilities & critical thinking.

Good to have :

• Experience as a statistician in the Life Sceince industry 
• Experience with clinical experimental design and statistical analysis
• Experience analyzing medical data, including clinical trial data, health insurance claims and/or electronic medical records.
• Experience with real-world evidence generation, HEOR studies and Health Technology Assessment (HTA)

Don't meet every job requirement? That's okay!

Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.

If you are looking to develop expertise in scientific consulting, build tomorrow tools in a young and dynamic environment, please send your CV and a cover letter.

Applications will only be accepted in English!