Overview
We are a private, newly created, and non-profit Foundation, linked to the Hospital Clinic de Barcelona, whose mission is to strengthen public health and improve the quality of life of citizens. To respond to our founding goals, we have an academic CRO for conducting clinical studies, initiated by the pharmaceutical and health technologies industry or by researchers, both in the field of medicines and medical devices, offering a comprehensive portfolio of services to meet the needs of our customers. We are looking for a talented and motivated Head of Biometry.
Main Responsibilities
- Lead and oversee all biometrics activities (in-house and outsourced), including biostatistics, statistical programming, and clinical data management.
- Develop and implement strategic directions for the department.
- Manage department budget, resources, and timelines.
- Ensure the quality, accuracy, and reliability of clinical data and systems.
- Establish and maintain the standards, policies, and procedures for the department.
- Accountable for all data management and statistics deliverables.
- Keeps abreast of new developments in clinical data collection, processing, storage, and retrieval to provide guidance in the selection, enhancement, and maintenance of data management tools and processes.
- Manage vendors for systems and software used by Data Management and Statistics teams.
- Serve as Project Manager for studies with only Data Management and / or Statistics services contracted.
- Ensures all deliverables are on time and on budget for all data management projects.
- Collaborate with cross-functional teams to support clinical development and regulatory submissions.
- Provide statistical input into clinical development plans, study designs, and data analysis.
Experiences and qualifications required
REQUIRED QUALIFICATION
Education (formal learning) - PhD in Biostatistics, Statistics, Mathematics, Data Science or a related field.Strong knowledge of statistical analysis methodologies, experimental design, and clinical trial expertise.Solid understanding of Good Clinical Practice.Knowledge of clinical studies regulatory framework.Knowledge of applicable data protection regulation.At least 10 years of experience in the biotechnology or pharmaceutical industry.Extensive experience designing and analyzing clinical trials, field studies, or experimental programs.Advanced English level; Desirable at least an advanced Spanish or Catalan level.Competence with software and hardware tools used in Data Management and Statistics processes.Familiarity with system validation execution and documentation.Strong leadership, strategic thinking, and communication skills; strong project management and organizational skills.Working conditions
Offices located in the center of Barcelona. Hybrid work (minimum of two days in the office).
Starting date of the contract : September / October 2025
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