As a Medical Writer Med Info - US, you will play a key part in developing, localizing, and maintaining high-quality US medical information content, responding to US and global Med Info enquiries and reviewing scientific content. You will collaborate closely with cross-functional teams, including US Scientific Affairs Communications, Medical Capability Process Excellence, and other global stakeholders, to ensure the accuracy, compliance, and scientific integrity of all medical information materials.
This is an opportunity to work in a fast-paced, international environment where your expertise in US medical communication standards and FDA regulations will directly impact the quality of information provided to healthcare professionals.
Join our General Services Medical Writing team as a Medical Information Writer, based in Barcelona (Sant Cugat), Spain, with a flexible working option.
**Tasks & responsibilities**
+ Produce new standard scientific response content (SSRC) or adapt global SSRC in accordance with company style guides, templates, and SOPs for US Medical Information content in designated therapeutic areas.
+ Update existing US-specific SSRCs annually or when new data becomes available, following direction from the US Scientific Affairs Med Info team.
+ Adjust content based on feedback during review cycles and contribute to peer (4-eye) reviews for content created by fellow writers.
+ Extract and share US Med Info reports from the enterprise platform for designated therapeutic areas, as defined by US Scientific Affairs.
+ Ensure the highest quality, accuracy, and fair balance of medical content, and contribute to cross-functional projects for continuous process improvement.
+ Respond to US and global medical information inquiries, including escalated inquiries from healthcare professionals, and review slide decks, scientific response documents, and medical affairs guidance documents.
**Requirements**
+ Experienced Medical Writer (3-5 years) with a scientific background and degree (PharmD, MD, PhD, or Masters), and at least 3 years of experience producing US Medical Information content.
+ Excellent medical writing skills and strong knowledge of FDA regulations, PhRMA guidelines, and other relevant US standards.
+ Strong attention to detail and accuracy; ability to manage and prioritize multiple, detailed activities; results-oriented with fast and focused execution.
+ Good communication, coordination, and time management skills.
+ Fluent in oral and written English, with a high level of communication skills.
+ Experience in writing and managing scientific publications (manuscripts, posters, abstracts, etc.) is desirable.
+ Prior experience in therapeutic areas such as Inflammation, Immunology, Pulmonology, Rheumatology, Oncology, Cardiovascular, Metabolism, Respiratory (CMR), Retinopathy, or Central Nervous System is advantageous.
\#IamBoehringerIngelheim because...
We are continuously working to design the best experience for you. Here are some examples of how we will take care of you:
+ Flexible working conditions
+ Life and accident insurance
+ Health insurance at a competitive price
+ Investment in your learning and development
+ Gym membership discounts
If you have read this far, what are you waiting for to apply? We want to know more about you!
All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.