Associate Director, Quantitative Clinical

Il y a 2 mois


Brussels, Belgique Amador Bioscience Temps plein

Amador Bioscience is a next-generation provider of translational research and clinical development solutions. As a global contract research organization (CRO) with established sites in the United States, Europe, and China, Amador confidently meets international clinical trial quality and compliance standards.

**Position Summary**

The Incumbent is an experienced quantitative clinical pharmacology leader to enhance and further our clinical pharmacology services globally through high-quality work, strategic client interactions, publications, and supervision of junior-level scientists. They will lead global pharmacometrics projects, provide technical guidance, and implement Model Informed Drug Development (MIDD) strategy for novel biotherapeutics across multiple therapeutic areas.

**Key Responsibilities**
- Lead a group of scientists to conduct translational and clinical PKPD modeling and simulations; contribute to MIDD strategy of clients for global biopharmaceutical development.
- Author, review, or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies if requested.
- Evaluate and implement new quantitative tools, software platforms, or technologies to facilitate clinical data analysis or clinical development decision-making.
- In collaboration with other function heads, develop technical training programs; supervise and provide training/guidance to junior-level scientists.
- Develop and maintain relevant SOPs and internal working practices to ensure compliance with regulatory requirements and industry standards.
- Establish and maintain professional relationships with global biopharmaceutical clients and Amador collaborators; contribute to Amador BD strategy and support BD activities.
- Lead Amador publication strategy, author or contribute to scientific publications, and present at external scientific or medical conferences.

**Qualifications and Education Requirements**
- Master/ Doctorate degree in pharmacometrics, clinical pharmacology, pharmaceutical sciences, medicine, statistics, chemical engineering, or related field.
- Approximately 7+ years of experience in Pharmacometrics Modeling )
- Experience:

- Proven experience in quantitative clinical pharmacology and implementation of modeling & simulations in biopharmaceutical development
- Experience with population PKPD modeling software (NONMEM, R, SAS, STAN, MATLAB, etc.)
- Excellent communication skills and organization skills are essential
- Special Skills/Abilities:

- Excellent problem-solving, written and oral communication skills.
- Prior leadership experience is desired but not required.

**Job Types**: Full-time, Permanent contract

**Benefits**:

- Company computer
- Eco vouchers
- Hospitalization insurance
- Retirement plan

Schedule:

- Monday to Friday

Ability to commute/relocate:

- 3500 Hasselt België: Reliably commute or planning to relocate before starting work (required)

Work Location: Hybrid remote in 3500 Hasselt België



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