About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Chiesi GRD in Parma, Italy, seeks an experienced SAS programmer to lead programming activities for clinical and safety data systems, supporting regulatory submissions and data warehouse initiatives. You will guide project-specific work plans, ensure data integrity, and collaborate
Etablissement : FIDEMECA Type de contrat : CDI Temps de travail : Temps plein Lieu: Sainte-Florence FIDEMECA, qui sommes-nous ? Passionné par le contrôle et la précision ? Jouez un rôle clé dans le contrôle et
Chiesi Farmaceutici S.p.A. in Parma, Italy, is seeking a Lead Statistical Programmer to drive SAS programming across clinical and safety data systems and prepare data packages for regulatory submission. You will lead project deliverables, ensure data quality and
Responsibilities Accountable for driving achievement of project milestones from study start‑up through to delivery of the database and monitoring of time spent on tasks. Provide Database Programming input into protocol data collection assessments. Create the annotated
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries,
IQVIA Laboratories is looking for a Lead Programmer (Centralized Monitoring Analyst) in Rome, Italy. The role requires at least 3 years of relevant experience in pharmaceutical research and a minimum of 2-3 years of SAS programming experience. You
Responsibilities Functions as a Lead Statistical Programmer, participates in SAS related programming activities for all clinical and safety data systems at Chiesi as well as activities in preparing data and metadata packages for regulatory submission. The Principal Statistical
Job Overview As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies. This involves planning and coordinating
IQVIA is seeking a Principal Statistical Programmer in Milano to lead complex statistical programming across studies. You will plan and develop integrated programming solutions, coordinate resources, and act as a technical lead for multiple projects, ensuring quality
Experteer Italy is seeking an accomplished Senior Statistical Programmer to lead programming efforts across complex studies and coordinate with SP teams and clients. You will translate requirements into specifications and guide development, testing, and documentation in a
Overview Experteer Overview: In this role you provide expert statistical programming to design and deliver integrated solutions for complex studies. You will lead programming efforts across studies, coordinate with SP teams and clients, and ensure high-quality
Experteer Overview In this role you lead the Database Programming team to design and deliver robust clinical databases and data checks across studies. You bridge scientific insight with data systems, ensuring timely, high-quality data delivery to
Experteer Overview In this role you will lead the Database Programming team and drive the clinical database development to collect data from paper or electronic CRFs. You will program computerized checks and SAS validations to ensure clean,
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor