Chargé de communication scientifique Cardio Rénal - CDI H/F
AmgenFrance - parisUpdate time: December 8,2021
Job Description
Career Category
Medical AffairsJob Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
Medical Communications Manager
What you will do
Purpose
•To deliver components of local Scientific Communication as defined by MedCom plans
•To provide ad-hoc MedCom support to the Affiliate brand team(s)
•To contribute to the development of local brand MedCom plans as component to the Medical / Brand plan
Context &reponsabilities
The Medical Communications Manager reports to the Medical Development Director and is reponsible for:
•Timely and high quality delivery of assigned SciCom deliverables and activities as a component of medical / brand teams based on local / regional strategies and team priorities
•Adherence to regulatory and legal regulations, SOPs, policies and guidelines
•Adherence to global and regional strategies
•Delivery of defined functional activities and adherence to functional guidelines
•Ensuring close cooperation with IHQ MedCom
•Planning and management of product MedCom budget
•Review/Approval of non-promotional and promotional materials as per SOPs
•Contributing to MedCom best practice development
Key Activities
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
•Reports on metrics and trends for assigned product(s)
•Review / approval of materials per SOPs
•Medical and Scientific materials and programs
•Scientific Symposia / workshops, incl’d digital
•Product Medical Communication 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
Decision Making Authority
•Financial payments as determined by grade level
•Within assigned products/areas, review/approval of materials as per SOPs
•Signs off on Medical Communication activities for product(s)
WIN
What we expect of you
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
Competencies
•Ability to work as part of a cross-functional team
•Excellent analytical and oral and written communication skills
•Strong organizational and planning skills
•Flexible and independent working style
•Solution-focused
•Science based
•Presentation skills
•Attention to detail
•Analytical skills and strategic thinking
•Customer-focused
THRIVE
What you can expect of us
As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.
- Vast opportunities to learn and move up and across our global organization
- Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
- Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
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