Chargé de communication scientifique - H/F
AmgenFrance - parisUpdate time: July 13,2021
Job Description

Career Category

Medical Affairs

Job Description

Non-Promotional & Promotional Materials

Provides input / guidance to commercial in the development of promotional materials with scientific content and reviews / approves promotional material as per SOP
Ensures local reviewing and approval of EHQ/global derived non-promotional items (such as slide decks), after local adaptation if needed
Ensures timely developing and delivering scientific contents, for internal and external usage based on plans and country needs
Reviews / approves non-promotional materials as per SOP
Partners with Medical Advisor in the development of non-promotional educational materials
Supports RML organization with tools and training for field based activities and RML plans

Support to educational activities

Supports/owns the development and delivery of affiliate satellite symposia and educational events
Participate in planning and implementation of satellite symposia and similar scientific/educational events, ensure high scientific standards and alignment with key messages
Provides congress support, including internal congress books, Medical CI collection, Medical booth materials, Post-congress information, such as web-ex and external congress reports
Supports planning and delivery of digital channel Medical activities in assigned area
Supports Advisory boards by delivering required materials

General & others

Supports the development and refinement of best practices and functional processes, systems and standards
Supports vendor management for MedCom related activities
Maintain and expand knowledge and expertise in relevant medical-scientific areas
Collects and provided metrics on the quality and quantity of delivered MedCom activities
Contributes to local MedCom planning, and execution
Manages allocated budget
Delivers or supports delivery of medical-scientific training for internal staff or vendors

Qualifications

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

Experience 

Minimum 2 years of professional experience (preferred  4 years), preferably in biotech/pharm. industry
Experience in multiple areas, including medical affairs or medical marketing and with international exposure
Experience in the development and delivery of symposia / educational programs and medical-scientific tools, such as slide decks
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

Knowledge

Broad scientific knowledge and specific knowledge relevant to assigned therapeutic area
Knowledge of regulatory / safety / legal requirements and implications of Medical Communication
Project management
Fluency in written and spoken English

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