
Haematology Therapies Specialist
12 hours ago
About this Role: As a Key Account Manager, you will be responsible for promoting GSK licensed Haematology product(s) in the assigned territory. You will work closely with the cross-functional team, developing and maintaining strategic account plans to support the appropriate use of our medicines.
Responsibilities:
- Promote and detail the value of GSK Haematology product(s) to target healthcare professionals (HCPs), including hospital physicians, nurses, pharmacists, and local payors where applicable.
- Utilize business acumen to analyse insights, sales data, and market research to set strategic direction and explore tailored initiatives.
- Develop and manage robust account plans to ensure successful launches and/or ongoing promotion of GSK Haematology products.
- Collaborate with cross-functional colleagues to maximise account opportunities or overcome barriers to achieve successful account performance.
- Implement an omnichannel approach across face-to-face, digital, and multimedia touchpoints, ensuring alignment with customer preferences.
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Medical Information Officer
11 hours ago
Oslo, Oslo County, Norway TN Norway Full timeCompany Overview:TN Norway is a leading player in the pharmaceutical industry, dedicated to improving patient outcomes through innovative solutions. Our Patient Safety & Pharmacovigilance (PSPV) aspiration is to be a cutting-edge safety group, enabling us to optimize the benefit-risk of our therapies.
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Medical Device Regulatory Lead
11 hours ago
Oslo, Oslo County, Norway TN Norway Full timeAre you passionate about regulatory affairs? Do you want to work in a dynamic global organization and collaborate with expert professionals?We are seeking a highly skilled Regulatory Affairs Specialist to join our team at TN Norway.About the Role:The successful candidate will be responsible for planning, managing, and tracking regulatory CMC submissions and...
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Regulatory Affairs Expert
11 hours ago
Oslo, Oslo County, Norway TN Norway Full timeWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at TN Norway.Job Description:The successful candidate will be responsible for planning, managing, and tracking regulatory CMC submissions and regulatory documentation. This includes Drug Master Files for raw, ancillary, and starting materials used in the manufacturing of cell and...