Medical Information Associate

<ul><li>Location: South Korea</li><li>Hiring Manager: Menai Johnson(<span>CO Medical Operations Lead SK &amp; ANZ)</span></li></ul><p></p><p><b><i>About the job</i></b></p><p></p><p><b>About Sanofi:</b></p><p>We’re an R&amp;D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.</p><p></p><p><i><b>Our Team:</b></i></p><ul><li><p><i>To provide high quality scientific information to internal and external customers.</i></p></li><li><p><i>To ensure high ethics and standards in our promotional materials aligned with medical strategy.</i></p></li><li><p><i>To enhance the quality of medical information initiative related to medical communication within Sanofi-Aventis Korea with an effective project management.</i></p></li></ul><p></p><p><i><b>Main responsibilities:</b></i></p><ul><li><p><i>To enhance the quality of medical information initiative related to medical communication within Sanofi-Aventis Korea with an effective project management.</i></p></li><li><p><i>Medical information</i></p><ul><li><p><i>Management of the preparation, review, approval, and maintenance of local standard response documents (i.e., Q&amp;A, FAQs, SRDs and other materials) for Sanofi products.</i></p></li><li><p><i>Management of Medical Information inquiries escalated by contact center to Sanofi personnel including review and approval of all written responses relating to Sanofi products for both internal and external customers.</i></p></li><li><p><i>First-line Medical Information enquiry handling.</i></p></li><li><p><i>Comply with Sanofi Pharmacovigilance and Quality reporting responsibilities by reporting all Adverse Events (AE) and Product Technical Complaints (PTC) within 24 hours of awareness.</i></p></li><li><p><i>Build collaborative and accountable relationships with key internal stakeholders (i.e., International, Global Medical Information and local Medical, Regulatory, Pharmacovigilance, Quality, Brand Teams)</i></p></li><li><p><i>Generate insights by identifying customers’ needs as the foremost contact point of customer communication. </i></p></li></ul></li></ul><p><i> </i></p><p><b><i>Promotional material review</i></b></p><ul><li><p><i>Review promotional materials from medical points of view ensuring quality and standards in line with local law, code and company quality documents.</i></p></li><li><p><i>Provide appropriate medical input to development of promotional materials and support to develop the claim aligned with marketing strategy.</i></p></li><li><p><i>Collaborate with and support regulatory, especially Ad. Promo Team, to contribute to ensure high ethics and standards in our promotional materials.</i></p></li><li><p><i>Drive strong collaborative relationships with commercial and cross-functional teams, including marketing and regulatory.</i></p></li></ul><p></p><p><b><i>About you </i></b></p><ul><li><i><span><b>Experience</b>:</span></i></li><li><i><span>Knowledge on products and related disease.</span></i></li><li><i><span>Knowledge on regulations and guidelines including pharmaceutical affairs law, guidelines of KPMA and KRPIA etc.</span></i></li><li><i><span>1-3 years experience in the pharmaceutical industry is preferred.</span></i></li><li><i><span><b>Education</b>: Majored in pharmacy or medical science preferred</span></i></li><li><i><span><b>Soft skills</b>:</span></i></li><li><i><span>Good communication skills</span></i></li><li><i><span>Writing and summarizing skills</span></i></li><li><i><span>Good project management skill</span></i></li><li><i><span><b>Technical skills</b>: Proficient computer skills (MS-Word, Power point, Excel)</span></i></li><li><i><span><b>Languages</b>: Well spoken &amp; written English</span></i></li></ul><p></p><p><b><i>Why choose us?</i></b></p><p></p><p><span><span>·<span>       </span></span></span><span>Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.</span></p><p><span><span>·<span>       </span></span></span><span>Work in a place that combines global scale with local expertise, backed by a strong culture of collaboration and shared purpose.</span></p><p><span><span>·<span>       </span></span></span><span>Join a team that’s not just transforming treatment - but asking what’s next, and making it real.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><h1>Pursue <i>progress</i>, discover <i>extraordinary</i></h1><p>Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.</p><p></p><p>At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.</p><p></p><p>Watch our <a href="https://www.youtube.com/watch?v&#61;SkpDBZ-CJKw&amp;t&#61;67s" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" target="_blank">sanofi.com</a>!</p>