Hot Medical Affairs Jobs

Medical Information Analyst Italian or French Speaking

Medical Information Analyst Italian or French Speaking Our client, a global pharmaceutical organisation based in Cork require a fluent Italian or fluent French speaker to join their Medical Information team. Fluency in English is also essential. As Medical Information Analyst you will combine your scientific knowledge and communication expertise in order to organize and deliver relevant medical communications to customers. Responsibilities Support Medical Information Services in Europe by professionally responding to medical/pharmaceutical inquiries from Health Care P...

Location: Cork,

Medical Information Product Specialist Fluent German, Spanish, Italian or French

Medical Information Product Specialist Fluent German, Spanish, Italian or French Our client, a global pharmaceutical organisation are currently recruiting for Product Specialist to join their medical information team. As Product Specialist you will be part of the European Medical Information organization and will act as the European Medical Information Subject Matter Expert (SME) with very comprehensive, detailed and specific subject matter knowledge. You will support the frontline Medical Information colleagues and ensures comparable standards for answers to customers within...

Location: Cork,

Publications Scientific Communications Associate

Publications Scientific Communications Associate Our client, a global pharmaceutical organisation are currently recruiting for a Publications Scientific Communications Associate to join their newly created Global Scientific Communications team. As Scientific Communications Associate you will work with cross-functional, multidisciplinary teams to prepare scientific publications including abstracts, posters, manuscripts and presentations and/or regulatory documents such as protocols, clinical study reports, briefing documents, regulatory responses, an...

Location: Cork,

CMC Regulatory Affairs Senior Manager

CMC Regulatory Affairs Senior Manager Our client, a global pharmaceutical organisation based in Cork are currently recruiting for a CMC Regulatory Affairs Senior Manager to join their global regulatory affairs group on a permanent basis. As CMC Regulatory Affairs Senior Manager you will manage the CMC submission management processes by leveraging expertise to optimize internal processes and tools. Responsibilities Manage the CMC submission management processes by leveraging expertise to optimize internal processes and tools processes and tools. Anticipate and resolve pr...

Location: Cork,

Regulatory Scientific Communications Associate

Our client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Associate to join their newly created Global Scientific Communications team. As Regulatory Scientific Communications Associate you will work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences including, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorization applications. Responsibilities Document Preparatio...

Location: Cork,

Scientific Communications Manager

Scientific Communications Manager Our client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Manager to join and manage a newly created Global Scientific Communications team. This is a challenging and rewarding opportunity, as Scientific Communications Manager you would work with thought leaders on external publications. Responsibilities • Function as an expert on publication industry standards and guidelines, such as Good Publication Practices, ICMJE requirements, and PhRMA guidelines • Provide publications ...

Location: Cork,

Regulatory Affairs Specialist

Our client a medical device early stage company wishes to add a Regulatory Affairs Specialist to our team. The successful candidate will work with the Design, Quality and Regulatory teams to support all regulatory functions for both existing and new products. Role/Responsibilities • Contribute to the regulatory strategy plans for new products, including required Regulatory Agency approvals. • Provide regulatory input into labelling, test strategies for new product development, risk analysis, clinical, preclinical and marketing issues. • Planning,...

Location: Cork,