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The US Medical Affairs Department is comprised of individuals devoted to partnering with health care professionals to generate evidence, to meet unmet needs and effectively engage scientifically to optimize patient outcomes. The intern will support the Neonatology medical team in its mission to address knowledge gaps important to our patients and the healthcare community
Posted Today
The Sr. Accounts Receivable Analyst is responsible for maintaining loyalty rebates process, calculation and posting of administrative fees, Credit Management, Collection and Dispute Analysis and reconciliation of general ledger accounts. Main Responsibilities Administrative Fees Calculate and prepare monthly/quarterly FFS/DSA fees to be paid to Wholesalers Generate GPO fe
Posted Today
To be selling agent within assigned territory, meet all sales objectives for Chiesi USA, Inc.'s promoted hospital products, and uphold standards and expectations of Chiesi USA. Cities to be based in Santa Barbara, Ontario, Pomona, San Bernardino, Woodland Hills, Glendale, Santa Clarita, and Ventura. Main Responsibilities In this role, you can expect to make Calls on targe
Posted Today
To be selling agent within assigned territory, meet all sales objectives for Chiesi USA, Inc.'s promoted hospital products, and uphold standards and expectations of Chiesi USA. Main Responsibilities In this role, you can expect to make Calls on targeted customers and promotes/sells Chiesi USA products in accordance with approved methods within assigned geographical territ
Posted 2 days ago
To be selling agent within assigned territory, meet all sales objectives for Chiesi USA, Inc.'s promoted hospital products, and uphold standards and expectations of Chiesi USA. Main Responsibilities In this role, you can expect to make Calls on targeted customers and promotes/sells Chiesi USA products in accordance with approved methods within assigned geographical territ
Posted 3 days ago
Support the Pharmacovigilance program with the collection and review of safety data from clinical trials and the set up of related documents in compliance with current regulations. Main Responsibilities Maintain and manage the relation with other Sponsors o oversight and support for all clinical trial pharmacovigilance activities o exchange and migration of safety data o
Posted 3 days ago
Support planning, execution and follow up of timelines and resources for GRA regulatory filings through product development and life cycle management Main Responsibilities Project Coordination Support Operational Excellence team members to execute regulatory project coordination and management, including agile ways of working, within GRA utilizing common templates and pro
Posted 6 days ago
This position will oversee the global eTMF (electronic Trial Master File) operations for GRD R&D including providing support to all study teams members involved in eTMF management. Responsible for creation and revision of all eTMF associated procedures, ensuring they are up to date and compliant with the applicable regulations. This position will assume the leadership rol
Posted 7 days ago
Reporting to the Global Dir Digital Engagement, the Digital Engagement Manager will play a pivotal role in shaping and executing the digital marketing operations for Chiesi Global Rare Disease (GRD). This individual will be at the forefront of digital strategy innovation, focusing on the development, measurement, and implementation of cutting edge digital marketing initia
Posted 7 days ago
The CPL is a permanent member of the cross functional R&D global Core Team (CT) who plays a key role in defining the target disease profile (TDP), target product profile (TPP), and the development and life cycle strategies of a given project. The CPL leads the Clinical Development Plan (CDP) Team (which consists of functional leaders from within GCD e.g. Clin Pharm, Clin
Posted 10 days ago
Job Purpose The Medical Science Liaison has the primary responsibility of building key opinion leader (KOL) partnerships by engaging in the exchange of scientific data and other medical and/or scientific information with external stakeholders (HCPs, researchers, professional organization leadership, and formulary decision makers) in the assigned Therapeutic Areas (TAs). S
Posted 10 days ago
The Global RA Manager (US Regional Regulatory Lead) contributes to the Company's success by managing the US Regional and in some cases global Regulatory strategy by providing regulatory guidance to the R&D Global Core Team as well as other non R&D functions. Main Responsibilities 1) Contributes to company success with collaboration from the Regulatory TA head 2) Accountab
Posted 10 days ago
This position will support Chiesi USA Value and Access team in developing, implementing and analyzing contracting strategies across all customer segments. Provide development opportunities, direction and guidance to Contracts Team. Review and approve contract set up, contract implementation and contract adjudication. Act as the subject matter expert on Contracts Operation
Posted 10 days ago
The Medical Science Liaison has the primary responsibility of building key opinion leader (KOL) partnerships by engaging in the exchange of scientific data and other medical and/or scientific information with external stakeholders (HCPs, researchers, professional organization leadership, and formulary decision makers) in the assigned Therapeutic Areas (TAs). Scientific en
Posted 15 days ago
Lead development and maintenance of global labeling processes ensuring compliance with applicable Health Authorities regulations and guidelines and internal company procedures and business objectives. Main Responsibilities Global Regulatory Product Labeling Lead activities to define and manage Chiesi's global labeling development and management strategy with an intended i
Posted 15 days ago
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