Salary Range:€30,200.00 - €56,000.00 Job Description Summary#LI-Hybrid Location: Ivera, Italy This role is based in Ivera, Italy. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all
Nestled in the picturesque surroundings of Collecchio, near the vibrant city of Parma, dsm-firmenich is proud to announce the opening of a cutting-edge production plant in early 2027. The new state-of-the-art facility will feature the latest
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr
Please submit your application in English What Youll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical
Overview As a Manager in IQVIA’s FIC team, you will oversee due diligence, valuation, asset screening, and growth strategy projects for biopharma and life sciences investments. You work closely with clients on high‑profile transactions, applying IQVIA
Novartis Farmacéutica in Ivrea, Italy is seeking an Associate Expert Science and Technology to execute microbiological activities in support of method validation and quality control. The role involves ensuring compliance with cGMP standards, performing microbiological analyses, and
#LI-Hybrid Location: Ivera, Italy. This role is based in Ivera, Italy. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. The Associate Expert Science and Technology
At Bryden Wood, we are expanding our team in Milan to work on large scale projects for the biggest names in the Data Centre and Pharmaceutical sectors. We are looking for an Associate Architect with site experience,
Position Summary We are looking for a candidate that will join our team as a QC Laboratory Technician. The QC Laboratory Technician is responsible for assisting in administration of the quality functions at a site to assure adherence
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all
Join to apply for the Advanced Packaging Engineer - Staff role at TDK InvenSense 3 days ago Be among the first 25 applicants Join to apply for the Advanced Packaging Engineer - Staff role at TDK
Chiesi è un gruppo biofarmaceutico internazionale focalizzato sulla ricerca, con 90 anni di esperienza e presente in oltre 30 Paesi, con sede centrale a Parma, Italia. Più di 8.000 collaboratori in tutto il gruppo sono uniti
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
Join to apply for the Advanced Packaging Engineer - Staff role at TDK Inven Sense 3 days ago Be among the first 25 applicants Join to apply for the Advanced Packaging Engineer - Staff role at