Job Overview With appropriate support and guidance: prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures, interpret analyses and write statistical sections of study reports. Develop and maintain programs to meet
Menarini Stemline is seeking a Data Management Specialist to join their Global Clinical Science department. This role involves developing and maintaining eCRF and data collection tools in alignment with clinical trial protocols and regulatory standards.Responsibilities include managing
Menarini Stemline is seeking a Data Management Specialist to join their Global Clinical Science department. This role involves developing and maintaining data collection tools in compliance with clinical trial protocols and regulatory standards.The ideal candidate will manage
Menarini Stemline in Borghetto Santo Spirito seeks a Data Management Specialist to develop and maintain the eCRF and data collection tools per clinical trial protocols. Responsibilities include managing system access and data validation for Phase I-III
Menarini Stemline in Udine is seeking a Data Management Specialist to join the Global Clinical Science department. In this role, you will develop and maintain data collection tools in accordance with clinical trial protocols and regulatory
Menarini Stemline in Bardi, Italy, is seeking a Data Management Specialist to develop and maintain eCRF and data collection tools. This role involves managing clinical trial data activities, ensuring compliance with CDISC standards, and acting as the main
A data management organization is seeking a Clinical Data Specialist in Novara, Italy. This permanent position involves managing and validating complex clinical datasets, ensuring data quality, and adhering to CDISC standards. Candidates should hold a relevant degree, have
Menarini Stemline in Bari, Italy, is seeking a Data Management Specialist to join their Global Clinical Science department. In this role, youll be responsible for developing and maintaining data collection tools in line with clinical trial
Menarini Stemline is seeking a Data Management Specialist in Milano to join their Global Clinical Science department. In this role, you will develop and maintain eCRF and data collection tools, ensuring compliance with clinical trial protocols
A global pharmaceutical company in Milan is seeking a Statistical Programmer to support the programming of outputs for clinical studies. This role requires a scientific degree and 3-5 years of experience in a CRO or pharmaceutical
Data Management Specialist Overview The Data Management Specialist will join Global Clinical Science department of Menarini Stemline, the R&D organisation of the Menarini Group. As a Data Management Specialist, you will develop and maintain the eCRF
The Data Management Specialist will join Global Clinical Science department of Menarini Stemline, the R&D organisation of the Menarini Group. As a Data Management Specialist, you will develop and maintain the eCRF and other data collection
This role is for upcoming future opportunities that may arise at Fortrea.As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III)
Fortrea is looking for a Senior Statistical Programmer in Italy to contribute to the successful delivery of clinical trials. This role involves developing and validating SAS programs and leading projects for innovative drug development. The position
Premier Research is looking for a Statistical Scientist Director to join our Biostatistics team. You will help biotech, medtech, and specialty pharma companies transform life‑changing ideas and breakthrough science into new medicines, devices, and diagnostics. What
Data Management Specialist The Data Management Specialist will join Global Clinical Science department of Menarini Stemline, the R&D organisation of the Menarini Group. As a Data Management Specialist, you will develop and maintain the eCRF and
Select how often (in days) to receive an alert: Senior Director, Clinical Biometrics & Analytics Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT
A leading global CRO is seeking a Principal Statistical Programmer based in Italy. In this role, you will oversee all programming activities for complex clinical trials, bringing over 5 years of experience in statistical programming. You
As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex projects for a renowned, innovative and global top pharmaceutical company. You will be involved in
Overview Clinical Data Specialist position based in Italy (Novara) in a permanent role. Role involves supporting the management, validation, and structuring of clinical and scientific data within research projects, working with complex datasets, ensuring data quality,