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Ergomed
501-1000 employees
About Ergomed
Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology.• 1,400+ highly qualified professionals• Global full-service CRO• 25+ years of experience• Therapeutic specialization in oncology• Strong expertise in rare disease trials• Robust clinical safety system• Choice of leading drug safety databasesOur key services include:• Clinical Research Services• Pharmacovigilance• Medical Information• Regulatory• Medical Writing• Site Management• Study Physician Support• Biostatistics• Patient Study Support
4 days ago
Principal Biostatistician
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Description
- Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications.
- We partner with small to midsize biotech companies to move promising therapies through early phase development.
- The Principal Biostatistician will be part of a collaborative team that works with the sponsor, PM, clinical team, data managers, medical writers, statistical programmers, and potentially many other team members to support the statistical needs of the assigned clinical study(ies).
- Responsibilities include maintaining oversight of all contracted statistical output and activities, acting as the study lead for multiple studies, and providing mentoring and support to junior statisticians.
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Requirements
- Master’s degree (or Higher) in biostatistics, statistics, mathematics or other related disciplines.
- General understanding and application of biostatistics in clinical trials.
- Strong previous related experience working in a Contract Research Organization.
- Communication skills.
- Presentation skills.
- Knowledge of the MS Office Suite.
- Proficiency in one or more statistical programming language (SAS Preferred).
- Collaboration across cross-functional teams.
- Good understanding of ICH and regulatory landscape.
- Knowledge of advanced statistical methods (e.g., survival analysis, logistic regression, and mixed models).
- Fluency in English.
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Benefits
- Work-life balance
- Collaborative team environment
- Opportunity to make an impact in clinical research