Medical Information Mgr - Amgen - Athens (Greece)

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Medical Information Mgr - Amgen - Athens (Greece)

Δημοσίευση από medlsc Την / Το Κυρ Ιαν 15, 2012 7:29 am

Medical Information Mgr - Amgen - Athens (Greece)

Job Description

The position is based on a temporary contract with a duration of 1 year. However, the contract could be renewed up to 2 years, on a yearly basis. Reporting currently to the Medical Director, the candidate's main purpose is to provide Medical Information for one or multiple products in an affiliate.

The main responsibilities are:


- Compliance with regulations, SOPs, and processes
- Management of external and internal Medical Information enquiries
- Implementation of applicable global / regional MedInfo content
- Adaptation, creation and maintenance of local Medical Information content
- Management of MedInfo Systems
- Literature support

The main responsibilities also include the following activities:


- Intake, processing, and responding to external and internal Medical information enquiries in compliance with regulations and company SOPs/guidelines
- Timely entry of enquiry data into Medical Information eSystem
- Timely triaging of AE/PC to the appropriate departments
- Adaptation of applicable regional/global Medical Information content to local regulatory requirements
- Version control, reviewing, and updating of Medical Information content
- Literature searches and summaries
- Based on global literature radars and alerts, communicates relevant literature to the local organization
- Analyzes Medical Information content needs
- Articulates content needs via work in regional / global Medical Information teams
- Provides training for Medical Information vendors on assigned products
- Supervises of outsourced MedInfo activities
- Content provision to Medical Information vendors
- Provides country metrics and interpretation
- Contributes to the development of Medical information tools, and best practices
- Provides training on enquiry management for other functions, e. g. sales
- Maintains and applies knowledge on regulations and codes affecting Medical Information
- Assesses requirements for Medical Information materials, such as reprints, including budget requirements.
- Plans Medical Information activities for assigned product(s)
- Maintains and expands product and TA knowledge
- Contributes to region-wide / global Medical Information projects and initiatives
- Planning and delivery of science-based product MedCom activities as a component of medical / brand teams based on local / regional strategies and team priorities
- Local publication planning
- Compliance with regulations, processes and SOPs
- Partnering and close cooperation with Medical Team and Brand Team members across functions, including Medical Information, other Scientific Affairs, Medical, and commercial functions
- Ensuring close cooperation with Internaltional headquarters MedCom and Scientific Publications
- Planning and management of product MedCom budget
- Review/Approval of non-promotional and promotional materials as per SOPs
- Contributing to MedCom best practice development

Other output activities are:

- Timely and high quality fulfillment of Medical Information enquiries
- Medical Information plans for assigned product(s)
- Maintains standard Medical Information content, based on and aligned with regional / global content
- Develops specific local Medical Information content in alignment with Int‘l Medical Information standards
- Reports on metrics and trends of Medical Information activities for assigned product(s)

Basic Qualifications


- The person will bring at least a MSc in pharmacy or life sciences or Medical degree.
- 2 years experience in bio(pharmaceutical) industry, including regulatory, safety, clinical, or Medical Information in (bio)pharmaceutical.

Preferred Qualifications

It is preferred to hold a PhD qualification in lifesciences and and/or have a proven track record of 4 years experience in Medical Information within bio(pharmaceutical)industry.

Knowledge in one or more of the areas below is preferred:

- Regulations and codes affecting Medical Information
- Delivery of customer-focused and compliant Medical Information content
- Scientific knowledge and specific knowledge at least in one relevant therapeutic area
- Analysis of medical-scientific literature
- Literature database searching
- Usage of IS systems required to perform the job

Company Description


Amgen discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, Amgen was one of the first companies to realize the new science's promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses.

Amgen pioneered the development of novel products based on advances in recombinant DNA and molecular biology, and launched the biotechnology industry's first blockbuster medicines. Today, as a Fortune 500 company serving millions of patients, Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness.

Additional Information

Posted:December 22, 2011
Type:Full-time
Experience:Not Applicable
Functions:Science
Industries:Biotechnology, Pharmaceuticals
Employer Job ID:13075BR
Job ID:2320158

Apply on Company Website

Πηγή: http://www.linkedin.com

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