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Role & Responsibilities• Implement national Medical Affairs strategy at regional level through structured local medical plans• Act as the scientific face of Novo Nordisk to healthcare professionals• Build, develop, and maintain strong scientific relationships with KOLs, diabetes specialists, and relevant stakeholders• Gather clinical insights by engaging with HCPs and attending scientific meetings• Communicate treatment trends, unmet needs, and actionable insights to internal cross-functional teams• Collaborate with marketing and sales teams to support brand strategy and product positioning• Provide medical and scientific input to anticipate market changes and recommend corrective actions• Design and deliver medical education and scientific training for physicians, allied HCPs, and internal teams• Provide scientific support to brand teams on clinical data interpretation and therapeutic positioning• Ensure all activities comply with local regulations, Novo Nordisk policies, and ethical standardsQualification• MD or MBBS from a recognised institutionExperience• Minimum 2 years of relevant experience in Medical Affairs (desirable)• Prior experience as Medical Science Liaison or Regional Medical Advisor preferredSkills• Strong therapeutic knowledge in diabetes, obesity, and metabolic disorders• Excellent scientific communication and stakeholder engagement skills• Ability to interpret clinical data and treatment paradigms• Strong analytical, planning, and execution capabilities• High ethical standards with strong compliance orientationAbout The Company• Novo Nordisk is a global healthcare company focused on diabetes, obesity, and metabolic diseases, Committed to improving patient outcomes through innovation and scientific excellence.

Role & Responsibilities• Act as a therapeutic area scientific expert in Immunology• Engage in peer-to-peer scientific discussions with leading specialists including physicians, pharmacists, hospital managers, and scientific society leaders• Continuously update knowledge on treatment guidelines, clinical studies, and patient treatment trends within Immunology• Identify emerging scientific concepts with potential future clinical impact• Develop and maintain strong relationships with Key Opinion Leaders and rising scientific experts• Execute external stakeholder engagement plans in collaboration with Commercial, Medical Affairs, HEMAR, GCO, Medical Information, and Pharmacovigilance teams• Communicate non-promotional scientific information related to products, pipeline, and R&D programs• Respond to unsolicited scientific queries using approved Medical Affairs resources• Organize and participate in medical education programs, speaker training, and advisory boards• Provide scientific training and ongoing medical support to sales representatives• Support Medical Affairs clinical activities including registries, real-world evidence studies, and non-interventional research• Assist with investigator-initiated studies, site identification, study setup, and follow-up• Gather field insights on treatment patterns and scientific trends and contribute to Medical Affairs strategy and business decision-makingQualification• MD / Physician / Pharmacist / Dentist• PharmD or Master’s degree in Pharmacy preferredExperience• Minimum 4+ years’ experience in a multinational pharmaceutical company• 1–2 years of Medical Science Liaison experience preferred• Experience in Immunology is an advantageSkills• Strong scientific knowledge in immunology and related therapeutic areas• Excellent peer-to-peer communication and presentation skills• Ability to build trusted relationships with external stakeholders• Strong analytical and strategic thinking skills• Proficiency in medical education, real-world evidence concepts, and clinical research support• High standards of ethics, compliance, and scientific integrityAbout The Company• Johnson & Johnson Innovative Medicine focuses on science-based advancements inspired by patient needs, Immunology division leads development of transformational therapies for immune-mediated diseases.

Role & Responsibilities • Serve as a scientific resource for Canadian experts in Dermatology and related autoimmune disorders • Respond to requests for in-depth scientific information from the medical community, including the latest research and updates on Lilly's pipeline • Gather feedback from Scientific Experts and Thought Leaders to inform Lilly's research and strategic direction • Develop and maintain mutually beneficial, peer-to-peer relationships with the scientific community • Effectively communicate advanced disease state and product information to scientific experts and healthcare professionals • Maintain technical expertise in the therapeutic area and engage in continuous learning through meetings and literature searches • Collaborate with internal teams such as Clinical Research Physicians, Real World Evidence Scientists, and Medical Education to address customer needs • Report clinical insights and customer questions to the medical and brand teams to inform business objectives • Ensure all activities are compliant with applicable guidelines, rules, and regulations Qualification • Advanced degree in health sciences (PhD, MD, PharmD) with 2-3 years of relevant clinical or therapeutic experience in dermatology OR • MSc in healthcare or professional designation (BScN, PT, RD, etc.) with 5+ years of relevant clinical experience in dermatology OR • Previous MSL experience with sound knowledge of the pharmaceutical industry Experience • Significant clinical or research work in autoimmune diseases, particularly Dermatology • Previous Medical Science Liaison experience is highly desirable Skills • Intellectual curiosity and in-depth knowledge of immunology/autoimmune disorders • Ability to critically appraise scientific information and literature • Strong presentation skills, with the ability to simplify complex scientific content • Demonstrated ability to build strong, collaborative relationships with external customers • Strong project management and teamwork skills • Familiarity with the academic community and medical research About The Company • Eli Lilly and Company is one of the top 10 largest pharmaceutical companies in the world, dedicated to improving the quality of life through innovative medicines. Known for its core values of excellence, integrity, and respect, Lilly operates with strong governance principles and ethical product promotion

Role & Responsibilities • Provide compliant communication and education on the company’s marketed and emerging product portfolio to meet educational and professional needs • Develop and maintain professional relationships with healthcare professionals (HCPs) and key decision makers • Conduct scientific exchange with Key Opinion Leaders (KOLs), Centers of Excellence (COEs), patient advocacy groups, and societies • Support the development and execution of customer-centric tactical medical engagement plans • Provide scientific and clinical education on relevant topics such as disease state, product information, and burden of illness • Collaborate with Medical Affairs and Commercial teams to provide scientific expertise and share insights in support of internal and external activities • Participate in clinical trials and evaluate Investigator Initiated Research proposals • Travel up to 70% (field-based position) to engage with healthcare professionals and stakeholders Qualification • Advanced degree in medical/biosciences (MD, DO, PharmD, PhD) • Minimum 3 years of relevant clinical or therapeutic experience • Minimum 1 year of MSL experience with primary emphasis on field-based scientific exchange Skills • Excellent communication skills with the ability to discuss drug information and disease state treatments confidently • Ability to collaborate across teams and build relationships with healthcare professionals and stakeholders • Strong problem-solving and analytical skillsWork Arrangements • Field-based position with up to 70% travel required (3-4 field days per week, occasional weekends) • Base salary: $150K to $180K/yr (based on education and experience level) • Additional benefits include medical, dental, vision, 401K with match, life insurance, PTO, and employee resource groups About The Company • Tris Pharma, Inc. is a leading U.S. biopharmaceutical company focused on developing and commercializing innovative medicines in ADHD, anxiety, pain, and addiction. Known for a robust pipeline of products in neuroscience and other therapeutic categories, with over 150 patents

Role & Responsibilities • Engage with Medical Experts (MEs) to educate them on medical/scientific information • Identify and map MEs/Key Accounts, pinpointing opportunities to involve MEs when a specific medical need arises • Develop and execute ME engagement plans aligned with the country strategy • Respond to unsolicited requests for information from MEs • Support Novartis clinical research programs and optimize trial execution • Provide scientific educational support to potential and actual study sites in collaboration with clinical operations • Serve as a medical resource to field matrix colleagues • Report technical complaints, adverse events, or special case scenarios related to Novartis products within 24 hours of receipt • Be flexible to be on the field (80%) across key areas within Egypt Qualifications • Medical Degree (MD), Ph.D. in Pharmacy, or PharmD is required Experience • 0-3 years of experience in a medical role is preferred Skills • Strong scientific knowledge and ability to educate Medical Experts on medical/scientific information • Ability to collaborate with clinical research teams and study sites • Excellent communication and interpersonal skills • Flexibility to engage in fieldwork (80% travel across Egypt) • Ability to handle adverse event reporting and technical complaints in compliance with company protocols About The Company • Novartis is a global healthcare company focused on reimagining medicine to improve and extend lives. The company is committed to providing high-quality medicines and is recognized for its strong research and development capabilities.

Role & Responsibilities • Develop and maintain interactions with Thought Leaders (TLs) and Healthcare Providers (HCPs) to answer scientific, unsolicited product, and HEOR-related questions • Execute medical interaction plans with Key Accounts (e.g., Army, Railways, CGHS) according to the needs of stakeholders and overall medical strategy • Present information to HCPs, ensuring medical accuracy and compliance with local procedures, ethical guidelines, and directives • Assess the medical landscape by meeting with Thought Leaders to understand their needs, clinical trials, and scientific activities • Collect and provide meaningful medical insights back to medical and commercial teams for strategy development • Report safety information, including adverse events, in accordance with BMS SOPs • Support the Country Medical Plan by executing medical plan activities and contributing to the development of scientifically meaningful medical programs • Provide scientific support and training to internal stakeholders (e.g., Commercial, Regulatory, HEOR, Market Access) • Support Clinical Trial Activities by identifying study sites and supporting patient recruitment • Collaborate in patient advocacy programs and contribute to creating patient education materials Qualifications • MBBS, MD, BDS, MDS (or equivalent degree) Experience • 1-2 years of Field Medical experience in medical affairs (preferred) • Experience in the Cardiovascular therapy area is a plus Skills • Ability to translate scientific and clinical data into valuable information for healthcare professionals • Strong communication and presentation skills • Ability to develop peer-to-peer relationships with TLs and other healthcare professionals • Knowledge of clinical trial design, process, and HEOR core concepts • Ability to quickly learn new subject areas and environments About The Company • Bristol Myers Squibb (BMS) is a global biopharmaceutical company focusing on discovering, developing, and delivering innovative medicines in oncology, immunology, cardiovascular disease, and fibrosis.

Role & Responsibilities • Exchange and disseminate scientific, educational, and research-related information to Thought Leaders (TLs) via innovative engagement tactics • Provide clarification and education on scientific data, study protocols, meeting abstracts, and professional literature • Participate in clinical trial-related activities, including company-sponsored and investigator-initiated research • Interact with Medical Societies and Advisory Boards, answering medical/scientific queries and organizing/supporting advisory board activities • Attend congresses and conventions, network with TLs, establish new contacts, and gather competitive intelligence • Plan and organize scientific training and education events/sessions with TLs within the therapeutic area • Contribute to the identification, profiling, segmentation, and engagement strategy of TLs based on product Medical Affairs plans • Prepare reports and track activities against agreed objectives Qualifications • Medical/dental education (MD, MBBS, BDS, MDS) Experience • Basic knowledge of the concerned therapy area (cardiology and related molecules) • Basic understanding of clinical trials, their design, and rationale • Ability to work independently and in a team environment, building productive relationships internally and externally Skills • Excellent presentation, written, and verbal communication skills • Ability to engage with Thought Leaders and provide scientific support • Strong organizational and reporting skills About The Company • Bayer is a leading global healthcare and pharmaceutical company with a focus on science-based innovation.The company strives to make a positive impact on patient outcomes through dynamic, collaborative work environments and cutting-edge solutions in healthcare.

Role & Responsibilities • Plan and execute field activities to disseminate medical knowledge on Rare Blood Disorders • Provide healthcare professionals with information on relevant clinical studies and treatment guidelines • Organize scientific meetings and lectures with stakeholders • Collaborate with Key Opinion Leaders (KOLs) on diagnostic and management strategies for patients with hemophilia • Gather insights from healthcare professionals and provide actionable feedback to Sanofi • Ensure compliance with ethical standards and regulations in the pharmaceutical market Qualifications • Advanced degree in a technical, scientific, or medical field (MBBS, MD, or equivalent) Experience • 2-4 years of experience in a medical or scientific liaison role, preferably within rare blood disorders Skills • Strong scientific knowledge in Rare Blood Disorders, particularly hemophilia • Proven ability to build relationships with Key Opinion Leaders and healthcare professionals • Experience in organizing and conducting scientific meetings and lectures • Strong communication and presentation skills • Ability to gather and analyze insights to inform business strategy About The Company • Sanofi is a global healthcare and pharmaceutical company specializing in innovative drug development and delivering high-quality medical products.

Role & Responsibilities • Engage healthcare professionals with impactful scientific discussions aligned to the medical strategy • Identify data gaps and opportunities for real-world evidence and precision medicine • Gather field insights to inform product strategy and evidence generation plans • Support clinical trial execution and site education initiatives • Collaborate with cross-functional teams to improve patient access and outcomes • Deliver tailored scientific content through digital and in-person channels Qualifications • Medical degree (MBBS, MD, or equivalent) • Solid understanding of healthcare systems, research procedures, and industry guidelines Experience • Minimum 3 years of experience in a medical function within a therapeutic area • Proven ability to apply digital solutions for stakeholder engagement and field medical insights Skills • Strong communication and presentation skills • Ability to engage healthcare professionals effectively • Knowledge of real-world evidence generation and precision medicine • Experience in clinical trial support and scientific content delivery About The Company • Novartis is a global healthcare company specializing in innovative drug development, patient-centered solutions, and delivering high-quality medical products.

Role & Responsibilities • Implement local medical plans by executing the national Medical Affairs strategy within your region • Establish and maintain scientific relationships with KOLs, diabetes specialists, and other relevant stakeholders to drive scientific exchange and advocacy for Novo Nordisk’s portfolio • Gather and communicate clinical insights by attending scientific meetings and engaging with HCPs to capture clinical needs, trends, and unmet needs • Collaborate with marketing and sales teams to sharpen product positioning and promotional tactics • Develop and deliver scientific training and educational activities for physicians and allied HCPs • Provide medical advice and support to the brand team and other internal stakeholders on clinical data, label information, and therapeutic positioning • Ensure compliance with local regulations, Novo Nordisk policies, and ethical standards for scientific engagement Qualifications • MD, MBBS from a recognized institution • Solid understanding of diabetes, obesity, and related metabolic disorders Experience • Minimum 2 years’ relevant experience in Medical Affairs (Desirable) • Experience in gathering clinical insights and supporting medical education/training activities Skills • Strong knowledge of diabetes, obesity, and related metabolic disorders • Ability to interpret clinical data and treatment paradigms • Excellent communication and relationship-building skills with KOLs and other stakeholders • Ability to collaborate with cross-functional teams in a medical and commercial context • Strong attention to compliance and ethical standards About The Company • Novo Nordisk is a global healthcare company, with a strong focus on diabetes, obesity, and other serious chronic conditions. With decades of experience, Novo Nordisk is dedicated to providing innovative treatments and improving the lives of patients worldwide.

Role & Responsibilities • Exchange and disseminate scientific, educational, and research-related information with Thought Leaders (TLs) proactively and reactively • Provide clarification and education of scientific data, study protocols, meeting abstracts, and professional literature, both on-label and off-label, in alignment with local regulations • Answer medical/scientific queries from Medical Societies regarding Bayer products • Organize, support, and participate in advisory boards • Attend congresses and conventions, interact with TLs, establish new contacts, and gather competitive intelligence • Plan and organize scientific education and training events with TLs within specific therapeutic areas or products • Contribute to internal understanding of specific TL interests and expertise within the medical community • Submit timely reports and track activities against agreed objectives • Provide external scientific support, training, and education where needed Qualification • Qualification in natural sciences or a medical background (MD, MBBS, BAMS, BDS, MDS) Experience • Basic knowledge of the concerned therapy area and related molecules • Basic understanding of clinical trials, their design, and rationale • Experience working independently and within a team environment • Ability to build productive relationships both internally and externally Skills • Excellent presentation and written and verbal communication skills • Ability to engage and influence thought leaders and stakeholders effectively • Proficiency in managing scientific data and presenting it clearly to diverse audiences About The Company • Bayer – A global leader in life sciences, Bayer is dedicated to driving innovation and improving lives through advanced solutions in healthcare and agriculture. The company values dynamic shared ownership (DSO) and fosters a work environment that prioritizes higher productivity, faster innovation, and better results. Bayer is committed to diversity and inclusivity, promoting fairness and respect at work.

Role & Responsibilities • Develop and maintain professional relationships with internal and external customers to provide medical and scientific support for AbbVie initiatives in oncology • Execute the Medical Affairs plan for India and provide scientific education and training across AbbVie’s oncology portfolio • Lead scientific communication with key therapy leaders and stakeholders, organizing advisory boards, facilitating clinical trials, and serving as a medical resource • Provide fair and balanced scientific information to healthcare professionals (HCPs) on AbbVie products • Facilitate educational and research activities for physicians and healthcare professionals regarding current and future AbbVie therapies • Collaborate with commercial teams to ensure the information and training needs of healthcare professionals are met • Present AbbVie product data to healthcare professionals, academic institutions, and researchers • Support research initiatives requested by AbbVie R&D, Clinical Operations, and Medical Affairs departments • Serve as an internal medical and scientific resource for developing disease-state and product communications • Support Round Table and Advisory Board sessions to ensure scientific and clinical data accuracy • Conduct ongoing training for medical affairs, field sales, and internal teams • Travel approximately 60% of the time for field-based activities Qualification • MD or MBBS (Medical degree) Experience • 2-3 years of post-qualification experience in Medical Affairs • Experience in the pharmaceutical industry or clinical research preferred • Experience working collaboratively in a cross-functional matrix structure • Demonstrated ability to convey technical information to individuals with varying degrees of scientific knowledge • Strong presentation and teaching skills • Ability to build and maintain strong relationships with healthcare professionals and stakeholders Skills • Strong analytical skills to evaluate and communicate key clinical data • Proficiency in Microsoft Office and other relevant technology systems • Ability to engage and influence thought leaders and internal teams About The Company • AbbVie – A global biopharmaceutical company dedicated to improving lives through innovative medicines and solutions. AbbVie operates across key therapeutic areas such as immunology, oncology, neuroscience, and eye care, with a strong commitment to research and patient care. The company values diversity and inclusivity, fostering a collaborative and innovative environment to address the medical challenges of today and tomorrow.

Role & Responsibilities • Lead medical affairs objectives in the assigned country, serving as an internal medical, technical, and scientific resource • Use medical and scientific information to facilitate physician engagement on clinical and scientific issues relevant to AbbVie’s products • Identify and develop professional relationships with thought leaders, academic centers, and researchers in assigned therapeutic areas • Work closely with commercial leaders and medical affairs teams to set priorities and define strategies • Present AbbVie product data to healthcare professionals, academic institutions, and researchers upon request • Support research initiatives, collaborating with AbbVie R&D, Clinical Operations, and Medical Affairs departments • Develop scientifically accurate, balanced, and compliant disease-state and product communications • Support Round Table and Advisory Board sessions to ensure the accuracy of clinical data • Conduct ongoing training for internal teams, including medical affairs and field sales • Travel approximately 60% of the time for field-based activities, serving as the local representative of the Global Medical Office Qualification • MD, MBBS, or Pharm D Experience • 2-3 years of post-qualification experience in the Medical Affairs function • Experience within the pharmaceutical industry or clinical research is preferred • Ability to work cross-functionally in a matrix structure and support multiple stakeholders • Strong presentation and teaching skills to convey technical information effectively • Demonstrated ability to develop and maintain strong relationships with key stakeholders • Experience in evaluating and communicating clinical data effectively Skills • Ability to convey complex scientific and clinical data to individuals with varying scientific knowledge • Strong analytical and problem-solving skills • Proficiency with technology and systems like Microsoft Office About The Company • AbbVie – A global leader in the pharmaceutical industry, AbbVie is committed to delivering innovative medicines that solve serious health issues today and address tomorrow’s challenges. The company is deeply involved in multiple therapeutic areas including immunology, oncology, neuroscience, and eye care, with a commitment to improving lives through advanced treatments and solutions.

Role & Responsibilities • Execute the Medical Affairs strategy for AbbVie’s oncology portfolio in India • Provide scientific education and training initiatives across AbbVie’s oncology portfolio • Engage proactively and reactively with healthcare professionals (HCPs), disseminating scientific, educational, and research-related information • Serve as the primary contact for medical and scientific inquiries related to AbbVie products • Organize and participate in advisory boards, congresses, and conventions, interacting with Thought Leaders (TLs) • Support clinical trials and research initiatives, providing scientific support to AbbVie R&D, Clinical Operations, and Medical Affairs • Maintain professional relationships with key opinion leaders (KOLs), academic institutions, and researchers • Facilitate the development and distribution of scientifically accurate, balanced, and regulatory-compliant product communications and materials • Provide field-based medical support for HCPs and contribute to the development of disease-state communications • Participate in the training of medical affairs, field sales, and internal teams on scientific and product knowledge • Travel approximately 60% of the time for field-based activities Qualification • MD or MBBS (Medical Degree) • Post-qualification experience in Medical Affairs or clinical research, preferably in oncology Experience • 2-3 years of experience in the Medical Affairs function or clinical research • Experience in the pharmaceutical industry or related clinical research settings is preferred • Strong presentation and teaching skills with the ability to effectively communicate clinical and non-clinical data • Ability to build and maintain relationships with internal and external stakeholders • Experience in scientific training, product management, and clinical communication Skills • Strong knowledge of oncology therapeutics and clinical trial processes • Ability to critically evaluate and effectively communicate key clinical data • Experience with MS Office applications and other technological systems • Excellent interpersonal and communication skills • Ability to work independently and within a team, managing multiple stakeholders About The Company • AbbVie – A global biopharmaceutical company focused on discovering and delivering innovative medicines that address serious health challenges, including oncology, immunology, neuroscience, and eye care. AbbVie is dedicated to transforming patients' lives with cutting-edge therapies and solutions in collaboration with healthcare professionals and researchers worldwide.

Role & Responsibilities • Engage proactively and reactively with Thought Leaders (TLs), providing scientific, educational, and research-related information on Bayer products • Disseminate and clarify scientific data, study protocols, meeting abstracts, and professional literature • Participate in clinical trial activities, including company-sponsored and investigator-initiated research • Answer medical/scientific queries from medical societies regarding Bayer products • Organize and support advisory boards and interactions with medical societies • Attend congresses and conventions to network with TLs, gather competitive intelligence, and establish new contacts • Plan and organize scientific training and educational events with TLs in specific therapeutic areas or product lines • Identify, profile, and engage TLs, contributing to the internal understanding of their interests and expertise • Prepare and submit reports, tracking activities against agreed objectives Qualification • MD, MBBS, BDS, MDS, or equivalent in medical or dental education Experience • Basic knowledge of stroke and neurology therapy areas and related molecules • Basic understanding of clinical trials, their design, and rationale • Experience working independently and in team environments, building productive relationships with thought leaders Skills • Excellent presentation, written, and verbal communication skills • Ability to engage with and educate internal and external stakeholders on scientific topics • Strong organizational skills to plan and execute educational activities About The Company • Bayer Zydus Pharma – A leading global healthcare and pharmaceutical company committed to improving lives through innovative therapies. Bayer Zydus Pharma focuses on research-driven solutions in multiple therapeutic areas, including cardiovascular, neurology, and other high-impact medical fields.

Role & Responsibilities • Execute medical affairs strategy in the assigned zone, with a focus on relevant therapeutic areas • Understand current practices, medicines in use, and trends by engaging with key customer contacts, attending scientific symposia, and reviewing therapeutic journals • Provide clear, non-promotional communication to internal and external customers, positioning BI Medical as a preferred partner • Execute key medical projects (e.g., IIS studies) to ensure efficient interaction with customers and key customer networks • Participate in the implementation of the local medico-marketing strategy • Identify and build relationships with key stakeholders (EEs) in the territory to promote BI products effectively • Provide medical and product expertise towards product registrations and new indications, working closely with regulatory authorities • Assist with the defense of marketed products and provide expertise to regulators, NGOs, and the press • Write, revise, and review labeling documents for pipeline and local products as per relevant SOPs • Assist regulatory affairs with EE access when appropriate Qualification • Medical degree (preferably in Pharmacology) or qualification in Life Sciences • MD in Pharmacology is preferred for candidates without doctoral qualifications • For professionals without a doctoral qualification, relevant field-based work experience of 10+ years with strong scientific expertise is also acceptable Experience • 0-3 years of experience in the pharmaceutical or healthcare industry • Scientific expertise in the diabetes therapy area is required Skills • Excellent interpersonal skills and the ability to build strong relationships • Basic IT knowledge, including proficiency with MS Office applications • Ability to communicate scientific information clearly and effectively About The Company • Boehringer Ingelheim Group – A global leader in the pharmaceutical industry, dedicated to improving patient outcomes through innovative therapies and products. The company provides comprehensive solutions in multiple therapeutic areas, including diabetes, oncology, and immunology, with a focus on scientific excellence and customer collaboration.

Role & Responsibilities • Focus on Myopia Management as a new category for Essilor, providing expertise on myopia-related products • Speak knowledgeably about the myopia category to Ophthalmologists, Optometrists, and Opticians • Train and support ECP (Eye Care Professionals) staff on myopia management products • Open doors and promote sales for new myopia products • Conduct regular training sessions for ECPs, Optometrists, Ophthalmologists, and their staff • Troubleshoot and support selling efforts through education and engagement • Drive sales volume and value for myopia management products in the India business unit • Collaborate with business and sales teams to enhance product visibility and adoption Qualification • Bachelor’s degree in Optometry, Medicine, or related field • Postgraduate qualification in Management (preferred) Experience • At least 5 years of experience in Optometry, specifically related to PAL (Progressive Addition Lenses) or EPS (Eye Perception Services) • Experience in marketing, product management, or training related to medical devices or FMCG • Experience in the India market is essential; APAC experience is a plus • Confidence to train others and influence key stakeholders Skills • Strong ability to train and influence others • Goal-driven and result-oriented with clear, fact-based decision-making skills • Ability to work in a collaborative, cross-functional environment • Strong communication skills in English; proficiency in local languages is a plus • Multilingual skills are advantageous About The Company • EssilorLuxottica – A global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. The company offers a wide range of high-quality vision care products, including renowned brands such as Ray-Ban, Oakley, Persol, and Vogue Eyewear, along with a network of retailers like Sunglass Hut and LensCrafters.

Role & Responsibilities • Serve as a key representative of the Medical Affairs function, providing scientific and clinical expertise on Bioscan Research's technologies and innovations • Communicate complex medical and scientific information to healthcare professionals (HCPs) in a clear, accurate, and compliant manner • Establish and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the field of traumatic brain injury • Collaborate with cross-functional teams to support clinical development, regulatory activities, and marketing efforts • Provide training and support to internal teams on the scientific and clinical aspects of the company's products • Monitor and report on trends in the field of traumatic brain injury and related medical advancements Qualification • Advanced degree in a relevant scientific or medical field (MD, PhD, or equivalent) Experience • Prior experience as a Medical Science Liaison or similar role in the pharmaceutical, biotechnology, or medical device industry • Experience in communicating scientific data to healthcare professionals • Knowledge in the area of traumatic brain injury or related fields Skills • Strong scientific and clinical knowledge, particularly in traumatic brain injury and neurotechnology • Excellent communication and interpersonal skills to engage with HCPs and KOLs • Ability to present complex scientific concepts in a clear and compliant manner • Strong problem-solving and critical thinking skills • Ability to work independently and collaboratively in a cross-functional environment About The Company • Bioscan Research – A company dedicated to improving traumatic brain injury patient outcomes through innovative technologies, including the machine learning-powered NIRS device, CEREBO, which aims to advance clinical understanding and treatment strategies for brain injury.

Role & Responsibilities • Build and maintain peer-level scientific relationships with Neuroscience KOLs • Drive high-quality scientific discussions across Parkinson’s disease, Multiple Sclerosis, migraine, and related indications • Support upcoming product launches, CMEs, and advisory board meetings • Conduct compliant scientific exchange with neurologists and HCPs • Generate actionable medical insights from field interactions • Collaborate cross-functionally with Medical Affairs, Marketing, and Commercial teams • Contribute to medical strategy execution and launch readiness Qualification • MBBS / BDS / PharmD / MSc / PhD Experience • 1–2 years’ experience in Medical Affairs or MSL roles • Neuroscience therapeutic experience preferred Skills • Strong scientific communication and presentation skills • Ability to engage neurologists and senior clinicians in scientific dialogue • Good understanding of clinical data and treatment paradigms • Self-driven and capable of working independently in the field • Willingness to travel within assigned territories Why Join • Opportunity to work with an innovation-driven neuroscience portfolio • Early exposure to launch excellence and strategic medical affairs activities • Direct impact on patient care through scientific engagement • Strong platform for long-term growth in Medical Affairs and leadership roles