The Medical Director (or Associate) Dermatology NA is part of the Medical Affairs HIDO Strategy team. The main responsibility of the role is to lead on the development and implementation of the Medical Affairs strategy and tactics for Epidermolysis Bullosa (and Dermatology) in NA. The role will be the internal and external subject matter expert for NA. Main Responsibiliti

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

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

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

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

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

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

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

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

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

We are currently seeking qualified and highly motivated individuals for the position Head of Patient Services, Americas, Rare Diseases, reporting to the Head of the Americas, Rare Diseases Business Unit. The Head of Patient Services is an important member of the Americas Rare Diseases Leadership Team and will lead the Chiesi's Patient Services Function in effort to delive

We are currently seeking qualified and highly motivated individual for the position of Medical Science Liaison (MSL)for the Midwestregionreporting to theHead of US Medical Science Liaison (MSL),Global Rare DiseaseUnit. The territory is MI, IN, KY, IL, MO, WI, IA, MN, KS, NE, SD, ND (would consider also anyone living in Co or WY) This position is remotely based. Maintain b

The Global RA Manager contributes to the Company's success by managing the Corporate R&D Pipeline (projects in R&D Development) by providing regulatory guidance to the R&D Global Core Team as well as other non R&D functions, as needed. Main Responsibilities 1) Contributes to company success with collaboration from TA head 2) Accountable for global/regional regulatory stra

Subject matter expert of Project management in the organization that has an impact on the coordination of a product or set of products life, at all stages of the product lifecycle. Responsible for coordinating the project team in translating the project strategy into an overall cross functional integrated plan and for providing routine base update of project status. Main

Accountable for coordination of the operational management of assigned projects in order to develop compounds in line with Chiesi goals and medical/scientific standards. Accountable for communication to all stakeholders on the progress of the study Accountable to maintain and respect budget according to study signed contract Main Responsibilities Making appropriate operat