Medical Communications Manager in England - Cambridge, United Kingdom

at Amgen

Medical Practice
Minimum Qualification
Required Experience
7 - 10 years
Employment Type
Male or Female
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Job Description

Timely and high quality delivery of assigned MedComm deliverables
Adherence to regulatory and legal regulations, SOPs, policies and guidelines
Adherence to global and International strategies
For delivery of defined functional activities and adherence to functional guidelines 

Develops and delivers assigned MedCom materials and tools, such as slide decks for internal and external usage
Partners with commercial in the development of scientific/medical promotional materials
Partners with Medical in the development of non-promotional educational materials
Supports the development and delivery of region-wide satellite symposia and educational events
Supports Advisory boards by delivering required materials
Contributes to medical/scientific CI collection and reporting and congresses
Attends and contributes to daily debrief sessions at congresses
Develops and delivers internal congress materials
Reviews promotional material as per SOP
Reviews non-promotional materials as per SOP
Participate in planning and implementation of satellite symposia and similar scientific/educational events, ensure high scientific standards and alignment with key messages
Provides ad hoc support for affiliates in the execution of region-wide MedCom programs
Ensures timely dissemination of tools to affiliates
Delivers or supports delivery of trainings 
Build and maintains relations to key opinion leaders
Maintain effective working relationship and alignment with affiliate and US counterparts
Supports MedCom vendor management
Maintain and expand knowledge and expertise in relevant medical-scientific areas
Actively supports the development of best practices, common standards, metrics and systems
Plans own activities and ensures alignment with overall MedCom and brand plan


PhD in a life science, Pharm D, MD or MSc with substantial additional biomedical background 

Proven industry professional experience, preferably in biotech/pharm. 

Industry experience in multiple areas, including medical affairs or medical marketing and with international exposure

Experience with interpretation of clinical trials and pre-clinical data

Experience in generation of science-based materials.

Basic knowledge of clinical trial conduct and top-line regulatory issues desirable 

Medical writer

Broad scientific knowledge and specific knowledge relevant to assigned therapeutic area

Fluency in written and spoken English

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