Medical Information Associate| MEA
About this opportunity
Career Category
Medical Affairs
Job Description
About the job
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 reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
MedInfo Associate | MEA (French Speaker)
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
Bachelor’s 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.
French Speaker
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.
careers.amgen.com
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.
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Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 194 comparable Associate Clinical Development roles across 37 biopharma companies.
Salary context
47 of 194 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 194 comparable roles
+ 23 more countries
Seniority mix
194 of 194 peers have a known seniority level
Therapeutic area mix
16 of 194 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.