Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as Project Manager Clinical Supplies to manage the end-to-end supply chain for clinical trials, ensure timely and efficient distribution of trial materials, maintain optimal inventory levels, and
About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved
Duties: · Create and maintain applications for required projects within the Data Visualization and Application Development team. · Responsible for creating and maintaining macros and programs used to create statistical programming deliverables, including SDTM. · Integrate
COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as Project Manager Clinical Supplies - To manage the end-to-end supply chain for clinical trials, ensure timely and efficient distribution of trial materials, maintain optimal inventory levels,
The Role Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its international
Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe,
The Role: Moderna Services, Inc. seeks a Sr. Manager, Clinical Data Management for its Cambridge, Massachusetts location. Here’s What You’ll Do: Lead data management activities for in-house and outsourced studies. Responsible for vendor oversight activities across
Job Description Principal Trial Manager (PTM) The Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as
At ASTEK Iberia , we are looking for a Clinical Trial Supply Manager (CTSM) to join our global Clinical Supply Chain team in the pharmaceutical sector . ¿Interesado en saber más sobre este trabajo? Desplácese hacia
At ASTEK Iberia , we are looking for a Clinical Trial Supply Manager (CTSM) to join our global Clinical Supply Chain team in the pharmaceutical sector . ¿Es este el siguiente paso en su carrera? Descubra