Medical Information Associate| MEA

HOW MIGHT YOU DEFY IMAGINATION

• If you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching manufacturing and delivering ever-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of. Join us.

MedInfo Associate MEA

Responsibilities:

• Responds to Medical enquiries received from different channels in compliance with regulations and company SOPs/guidelines including performing literature searches and timely triage of associated AE/PC.
• Ensures that every medical information enquiry is adequately tracked and fully documented in Amgen Medical Information database.
• Assists in audit/inspection and ensuring preparedness.
• Facilitates expanded access requests as appropriate.
• Supports the delivery of exceptional patient and HCP support by efficiently managing medical enquiries ensuring quality standards are maintained and content is accurate up to date evidence-based and informative.
• Maintains and applies knowledge on regulations and codes affecting Medical Information.
• Maintains and expands product and TA knowledge.
• Adapts and maintains local/regional content per local/regional requirements.
• Reports on trends/insights for assigned product(s).
• Supports Amgen partners operations processes systems and training.
• Leads/contributes to local/regional Medical Information projects and initiatives as assigned.
• Collaborates with cross-functional partners on shared goals and activities.

Qualifications

Minimum Requirements

• Bachelors degree in Pharmacy or Life Sciences/healthcare-related field.
• Minimum 2 years of experience in MedInfo or any other relevant healthcare setting within the pharmaceutical industry.
• Advanced English language skills verbal and written.

Preferred Requirements

• French Fluency is highly desirable.
• Proficiency in scientific literature searching critical review of clinical studies and interpretation of published data.
• Excellent verbal and written communication skills.
• Strong attention to details.
• Research and analytical skills.
• Ability to handle multiple tasks and competing priorities.
• Demonstrated time management skills.
• Ability to work in a team environment and/or independently as needed.
• Solid skills in conducting comprehensive literature searches and in critically appraising scientific literature.
• Sound working knowledge of ethical legal and regulatory guideline and requirements applicable to medical affairs activities.
• Experience in the biopharmaceutical industry and/or strong knowledge of the pharmaceutical drug development process.
• Proficient in Outlook PowerPoint Excel Word software programs Salesforce Databases.

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

Apply now for a career that defies imagination

In our quest to serve patients above all else Amgen is the first to imagine and the last to doubt. Join us.



Amgen is an Equal Opportunity employer and will consider you without regard to your race color religion gender sexual orientation gender identity national origin protected veteran status or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request an accommodation.