Medical Science Liaison

h3Job Function: /h3pMedical Affairs Group /ph3Job Sub Function: /h3pMedical Science Liaison /ph3Job Category: /h3pScientific/Technology /ph3All Job Posting Locations: /h3pBeerse, Antwerp, Belgium, Diegem, Flemish Brabant, Belgium /ph3Job Description: /h3pMedical Science Liaison (MSL), located in Belgium Field-based role (Belgium and Luxembourg) Full time /ppJohnson Johnson Innovative Medicine BeLux is recruiting for a Medical Science Liaison (MSL), located in Belgium. In this exciting role as MSL within our Medical Affairs (MAF) BeLux team you engage with Leading Specialists and other healthcare professionals in high-quality, non-promotional scientific exchange. You provide fair, balanced and objective scientific information and education, discuss our products and the supporting evidence, and help enable the right treatment for the right patient at the right time. You will build scientific relationships, identify medical insights and bring those insights back into our Medical Affairs and Core Value Team strategy. Your work contributes to the Medical Affairs Plan and to our short
- and long-term company goals. All MSL interactions are non-promotional. Your scope may evolve with business needs. You may work across therapeutic areas, products or territories within BeLux. This means quickly getting up to speed on new science, data and stakeholder networks while ensuring continuity in existing relationships. This is a field-based role, within Belgium and Luxembourg, with 70–80% of your time spent in the field. You will work closely with Medical Affairs colleagues and cross-functional partners and report to the Medical Therapeutic Area Lead (MTAL). /ph3Key

Responsibilities:
/h3ulliDrive scientific exchange and generate insights. /liliPrepare and lead interactions with Leading Specialists. /liliProactively and reactively discuss relevant scientific information in line with healthcare compliance guidelines, drive scientific alignment and identify actionable medical insights. /liliBring these insights back into Medical Affairs strategy, tactical plans and integrated account planning. /liliSupport data, information and evidence generation. /liliRespond to unsolicited scientific questions and support clinical research, from PI/site selection and study feasibility to site engagement and issue resolution for RD clinical trials and Medical Affairs studies, as appropriate. /liliContribute to real-world evidence generation, patient-value initiatives, early-access and risk-management programs, as well as customer support requests such as educational grants, and investigator-initiated studies. /liliBring medical education to life from start to finish. /liliIdentify educational needs, define concepts and objectives, engage collaborators and speakers, plan and deliver compliant medical education initiatives, and evaluate their impact. /liliCollaborate and deliver. Work closely with Medical Affairs and cross-functional partners. /liliSet priorities, take ownership of your work and continue developing your expertise. /liliEnsure that all activities comply with applicable legal, HCBI, safety-reporting, company-policy and SOP requirements. /li /ulh3Qualifications

Education:
/h3pScientific degree : Medical doctor, pharmacist or degree in life sciences (with MD/PhD being an additional asset) /ph3Experience and

Skills:
/h3pScientific and clinical knowledge to quickly understand new disease areas, compounds, clinical trial designs and complex medical data. Can translate data into relevant, balanced scientific discussions with healthcare professionals. Adapt quickly to different therapeutic areas, products, stakeholder networks and territories as business needs evolve. Can build effective relationships with internal and external partners and maintain a strong customer focus and business insight. Understands the healthcare environment and identify relevant opportunities for Medical Affairs. Understand clinical research, clinical trial execution and Good Clinical Practice. Work effectively across functions while taking ownership of your own priorities and activities. Act proactively and manage your work independently, with a clear focus on delivery. Work with integrity and follow JJ Credo values, applicable regulations and HCBI guidelines. /ph3Other

Requirements:
/h3pYou are fluent in Dutch, French and English, both spoken and written, to support stakeholders across BeLux. The role involves 70–80% travel within Belgium and Luxembourg and requires a valid driver's licence. /ph3About the Opportunity: /h3pReady to make an impact? If you want to leave your personal mark and be valued for who you are, Johnson Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career and where you feel you can bring your whole self to work. We provide you an environment to fulfil your career aspirations as