Medical Science Liaison Jobs

Role & Responsibilities• Plan, prepare, and engage with Thought Leaders (Doctors) to exchange scientific, educational, and research-related information• Proactively and reactively disseminate, clarify, and educate on scientific data, study protocols, abstracts, and professional literature in line with local regulations• Respond to medical and scientific queries from Medical Societies related to assigned products• Organize, support, and participate in advisory board meetings• Attend congresses and conventions to network with healthcare professionals and gather competitive intelligence• Plan and coordinate scientific training and education sessions within the assigned therapeutic area or product• Identify, profile, segment, and engage Thought Leaders in alignment with the Medical Affairs plan• Contribute insights on Thought Leader interests and expertise to support internal medical strategy• Prepare and submit timely reports and track activities against agreed objectives• Provide additional external scientific support, training, and education as requiredQualification• Qualification in Natural Sciences OR Medical background (MD, MBBS, BAMS, BDS, MDS)Experience• Experience in Medical Affairs, Medical Science Liaison, or scientific engagement roles preferredSkills• Basic knowledge of the Diabetology therapy area and related molecules• Understanding of clinical trials, including study design and scientific rationale• Strong presentation, written, and verbal communication skills• Ability to work independently and collaboratively in a team environment• Strong internal and external stakeholder relationship-building skillsAbout the CompanyBayer is a global life science organization driven by the mission of achieving Health for all and Hunger for none. With a strong focus on innovation, scientific excellence, and sustainability, Bayer fosters a diverse and inclusive work environment while delivering meaningful impact across healthcare and agriculture worldwide.

Role & Responsibilities• Align Medical Affairs strategies with Haleon’s business objectives across the India Consumer Healthcare portfolio• Engage in non-promotional, scientific discussions with healthcare professionals across relevant specialties• Build, develop, and maintain strong relationships with Key Opinion Leaders and medical experts• Represent the organization at CMEs, advisory boards, training-of-trainers programs, and medical conferences• Generate actionable medical insights through routine HCP interactions, surveys, and field intelligence• Support clinical trial activities, investigator engagement, and medical research initiatives• Deliver scientific training, product knowledge, and medical insights to internal stakeholders• Collaborate with medical associations and contribute to guideline development initiatives• Ensure all scientific engagements comply with internal SOPs, ethical standards, and regulatory requirementsQualification• MBBS or BDS OR Postgraduate degree in Pharmacy, Life Sciences, or related medical discipline (Pharm.D, M.Pharm, MSc Life Sciences)Experience• Minimum 1+ year of experience in Medical Affairs, Medical Science Liaison, Clinical, or Scientific rolesSkills• Strong interpersonal, analytical, and communication skills• Effective scientific presentation and storytelling abilities• Proficiency in MS Excel and PowerPoint• Ability to manage multiple priorities in a fast-paced, field-based environment• Strong stakeholder engagement and relationship management capabilitiesAbout the CompanyHaleon is a global, science-led consumer healthcare company known for trusted brands such as Sensodyne, Voltaren, Centrum, Panadol, and Advil. With a strong commitment to integrity, transparency, and patient focus, Haleon combines scientific excellence with a consumer-first mindset to deliver better everyday health through innovation, collaboration, and a people-centric culture.

Role & Responsibilities• Plan, prepare, and engage with Thought Leaders (Doctors) to exchange scientific, educational, and research-related information• Proactively and reactively disseminate, clarify, and educate on scientific data, study protocols, abstracts, and professional literature in line with local regulations• Respond to medical and scientific queries from Medical Societies related to assigned products• Organize, support, and participate in advisory board meetings• Attend and actively participate in congresses and conventions to network with healthcare professionals and gather competitive intelligence• Plan and coordinate scientific education and training sessions within the assigned therapeutic area• Identify, profile, segment, and engage Thought Leaders in alignment with the Medical Affairs plan• Contribute insights on Thought Leader interests and expertise to support internal strategy development• Prepare and submit timely activity reports and track performance against agreed objectives• Provide additional external scientific support, training, and education as requiredQualification• Qualification in natural sciences or medical background (MD, MBBS, BAMS, BDS, MDS)Experience• Prior experience in Medical Affairs or scientific engagement roles preferred• Exposure to therapy area engagement and healthcare professional interactionsSkills• Basic knowledge of the Diabetology therapy area and related molecules• Understanding of clinical trials, including design and scientific rationale• Strong presentation, written, and verbal communication skills• Ability to work independently and collaboratively in cross-functional teams• Strong relationship-building skills with internal and external stakeholdersAbout the CompanyBayer is a global life science company driven by a mission to achieve Health for all and Hunger for none. With a strong focus on innovation, scientific excellence, and sustainability, Bayer works across healthcare and agriculture to address some of the world’s most pressing challenges while fostering a diverse, inclusive, and respectful work environment.

Roles & Responsibilities• Establish and maintain peer-level scientific relationships with oncology Key Opinion Leaders across academic and private institutions• Deliver compliant, impactful, and timely scientific interactions aligned with the medical strategy• Act as therapeutic expert across multiple oncology indications including renal, lung, breast, prostate, and ovarian cancers• Support regional medical education programs and scientific initiatives• Provide clinical and scientific expertise to cross-functional teams including Medical, Commercial, Market Access, Regulatory, and Pharmacovigilance• Collect and analyze actionable field insights to refine and optimize medical strategy• Ensure accurate reporting of adverse events and product complaints in line with SOPs and regulatory requirements• Support launch activities for new oncology assets and innovator molecules• Participate in national and international oncology congresses and scientific meetings• Contribute to territory reviews, scientific planning, and medical strategy alignment sessions• Maintain accurate documentation and ensure compliance with company policies and industry standards• Travel extensively (60–70%) across assigned territories as requiredQualification• BDS / MBBS / PharmD / MSc / PhD in Life Sciences or Clinical ResearchExperience• Minimum 12 to 16 years of experience in Medical Affairs or as a Medical Science Liaison• Prior experience in oncology or specialty care is mandatory• Exposure to oncology product launches or targeted therapies preferredSkills• Strong scientific acumen with deep knowledge of oncology and Indian healthcare ecosystem• Excellent communication, interpersonal, and presentation skills• Ability to interpret and present complex clinical and scientific data• Strategic thinking with agility to execute field initiatives• Proficiency in Microsoft Office, CRM tools, and digital engagement platforms• Strong stakeholder management and cross-functional collaboration skillsAbout the CompanyAmneal Pharmaceuticals, Inc. is a global pharmaceutical organization focused on developing, manufacturing, and delivering high-quality generic and specialty medicines. With a strong presence across key therapeutic areas, including oncology and specialty care, Amneal is committed to improving patient access to affordable, effective treatments while upholding rigorous standards of science, compliance, and patient safety.

Roles & Responsibilities• Engage healthcare professionals through high-quality scientific discussions aligned with medical strategy• Identify data gaps and opportunities for real-world evidence and precision medicine initiatives• Gather and communicate field insights to support product strategy and evidence generation plans• Support clinical trial execution, site education, and investigator engagement activities• Collaborate cross-functionally with medical, commercial, and access teams to improve patient outcomes• Deliver tailored scientific content via digital platforms and in-person engagements• Maintain accurate documentation of field medical activities in compliance with internal and regulatory requirementsQualification• Life sciences or medical qualification (MBBS / MD / PharmD or equivalent preferred)Experience• Minimum 3 years of experience in a medical or scientific function within a therapeutic area• Experience working within healthcare systems and clinical research environments preferredSkills• Strong understanding of healthcare systems, research processes, and industry guidelines• Ability to identify and apply real-world evidence insights• Experience using digital tools for stakeholder engagement and medical insights• Excellent scientific communication and presentation skills• Strong interpersonal skills and cross-functional collaboration abilityAbout the CompanyNovartis is a global healthcare leader focused on reimagining medicine to improve and extend people’s lives. With a strong emphasis on scientific innovation, research excellence, and patient-centric solutions, Novartis delivers high-quality therapies across multiple therapeutic areas while fostering a culture of learning, collaboration, and professional growth.

Roles & Responsibilities• Plan, prepare, and engage with Thought Leaders (Doctors) as a scientific partner through proactive and reactive interactions• Disseminate, clarify, and educate on scientific data, study protocols, meeting abstracts, and professional literature in line with local regulations• Handle unsolicited off-label scientific discussions in compliance with applicable guidelines• Respond to medical and scientific queries from Medical Societies related to Bayer products• Organize, support, and participate in advisory board meetings• Attend congresses and conventions to network with Thought Leaders and gather competitive intelligence• Plan and coordinate scientific education and training sessions within the diabetes care therapeutic area• Identify, profile, and segment Thought Leaders to support engagement strategy and medical affairs planning• Contribute insights on Thought Leader interests and expertise to internal Medical Affairs teamsQualification• Medical background with MD / MBBS / BDS / MDSExperience• Minimum 1+ year of relevant experience• Experience in Medical Affairs or scientific engagement preferredSkills• Basic knowledge of Diabetes and related therapy areas• Understanding of clinical trials, study design, and rationale• Strong presentation and scientific communication skills• Excellent written and verbal communication abilities• Ability to work independently and collaboratively in cross-functional teams• Strong relationship-building skills with internal and external stakeholdersAbout the CompanyBayer is a global life sciences organization with core competencies in healthcare and agriculture. Driven by innovation and a strong commitment to science, Bayer focuses on developing solutions that improve health outcomes and quality of life.

Roles & Responsibilities• Act as an internal medical, technical, and scientific resource leading Medical Affairs objectives for the oncology portfolio in India• Execute Medical Affairs plans by providing scientific education and training initiatives across AbbVie oncology products• Develop and maintain strong professional relationships with healthcare professionals, therapy leaders, academic centers, and researchers• Lead scientific discussions and provide fair, balanced, and non-promotional scientific information to healthcare professionals• Organize and support advisory boards, round table discussions, and scientific meetings• Facilitate information, education, and research activities related to current and future oncology therapies• Support clinical research initiatives in collaboration with AbbVie R&D, Clinical Operations, and Medical Affairs teams• Present clinical and scientific data to physicians, academic institutions, and other healthcare professionals upon request• Serve as an internal medical resource for disease-state and product communications ensuring regulatory compliance• Collaborate closely with commercial leaders, therapeutic leads, and Medical Affairs leadership for planning and prioritization• Provide ongoing medical and scientific training to medical affairs, field sales, and internal teams• Ensure accurate and timely documentation of medical affairs activities• Manage medical affairs activities within assigned annual budget parameters• Ensure full compliance with AbbVie internal policies, ethics, and applicable regulatory requirements• Represent Global Medical Office functions locally, including pharmacovigilance and HEOR activities• Undertake extensive field engagement with approximately 60% travel requirementQualification• MD or MBBSExperience• Minimum 2 to 3 years of post-qualification experience in Medical Affairs• Pharmaceutical industry or clinical research experience preferred• Experience working cross-functionally in a matrix organizationSkills• Strong scientific communication, presentation, and teaching skills• Ability to interpret and communicate clinical and non-clinical technical information effectively• Strong relationship-building and stakeholder engagement skills• Analytical skills for critical evaluation of clinical data• Ability to work collaboratively with multiple internal and external stakeholders• Proficiency in Microsoft Office and medical affairs systems• High ethical standards and compliance-oriented mindsetAbout the CompanyAbbVie is a global biopharmaceutical organization dedicated to discovering and delivering innovative medicines that address serious health challenges across oncology, immunology, neuroscience, and eye care, along with solutions from its Allergan Aesthetics portfolio.

Roles & Responsibilities• Act as the internal medical, technical, and scientific resource leading Medical Affairs objectives for assigned therapeutic areas• Engage physicians, researchers, and healthcare professionals using medical and scientific expertise related to AbbVie products• Identify, develop, and maintain professional relationships with thought leaders, academic centers, and researchers• Present scientific and clinical data on AbbVie products to healthcare professionals and institutions upon request• Support research initiatives in collaboration with AbbVie R&D, Clinical Operations, and Medical Affairs teams• Serve as a medical resource for disease-state and product communications ensuring accuracy, balance, and regulatory compliance• Support advisory boards, round table discussions, and scientific meetings• Provide ongoing medical training to field sales, medical affairs, and other internal teams• Collaborate closely with commercial leaders, therapeutic leads, and Medical Affairs leadership for business planning and prioritization• Ensure accurate and timely documentation of all medical affairs activities• Manage annual medical affairs activities within assigned budget parameters• Ensure full compliance with AbbVie ethics, internal policies, and all applicable regulatory requirements• Represent Global Medical Office functions locally, including PV and HEOR activities• Undertake extensive field work, with approximately 60% travel requirementQualification• MD / MBBS / PharmDExperience• Minimum 2 to 3 years of post-qualification experience in Medical Affairs• Pharmaceutical industry or clinical research experience preferred• Experience working cross-functionally in a matrix organizationSkills• Strong scientific communication, presentation, and teaching skills• Ability to interpret, analyze, and communicate clinical data effectively• Strong relationship-building and stakeholder engagement skills• Ability to work collaboratively with multiple internal and external stakeholders• Proficiency in Microsoft Office and medical affairs-related technologies• High ethical standards and compliance-focused mindsetAbout the CompanyAbbVie is a global biopharmaceutical organization focused on discovering and delivering innovative medicines that address serious health conditions across immunology, oncology, neuroscience, and eye care, along with solutions from its Allergan Aesthetics portfolio.

Roles & Responsibilities• Plan and execute scientific field activities to provide healthcare professionals with up-to-date medical knowledge on rare blood disorders, with a focus on hemophilia• Lead high-quality scientific discussions and disseminate recent clinical evidence and treatment guidelines• Build and maintain strong, science-based relationships with healthcare professionals and key stakeholders• Organize and support scientific meetings, lectures, and educational programs within the therapeutic area• Support healthcare professionals in the diagnosis and management of patients with hemophilia• Collaborate on speaker training programs and gather insights on treatment trends and unmet needs• Align scientific field activities with the company’s medical and strategic objectives• Work cross-functionally with internal teams to ensure consistent and compliant scientific communicationQualification• Advanced degree in a scientific or medical field (MBBS, MD preferred)Experience• 2 to 6 years of relevant experience• Prior experience as a Medical Science Liaison or Scientific Advisor in the pharmaceutical industry preferred• Experience or knowledge of Hematology / Hemophilia strongly preferredSkills• Strong scientific and clinical knowledge in rare blood disorders• Excellent communication and presentation skills• Strategic planning and proactive engagement capabilities• Ability to analyze data and develop effective engagement plans• Strong teamwork and cross-functional collaboration skills• Proficiency in English (written and spoken)About the CompanySanofi S.A. is a global healthcare leader dedicated to pursuing progress and discovering extraordinary solutions to improve patient lives. With a strong focus on innovation, science, and patient-centric care, Sanofi works across diverse therapeutic areas while fostering a culture of diversity, equity, and inclusion, empowering professionals to make a meaningful impact in the world of medicine.

Roles & Responsibilities• Maintain strong knowledge of legislation relevant to the pharmaceutical ecosystem• Generate and communicate high-quality medical and scientific evidence to HCPs• Engage scientific discussions with key stakeholders across the patient journey• Support evidence-based adoption of therapies in Cardiovascular, Renal, and Metabolic areas• Collaborate cross-functionally with medical, commercial, and market access teams• Act as a scientific partner to physicians, ensuring ethical and compliant interactions• Contribute to improving patient outcomes through scientific exchange and insight generationQualification• Bachelor’s degree in Pharmacy or Medical SciencesExperience• Minimum 3 years of experience in a multinational pharmaceutical environment• At least 1 year of experience as a Medical Science Liaison or Medical Advisor• Experience in Cardiovascular / Renal / Metabolic therapy areasSkills• Strong understanding of pharmaceutical legislation and compliance• Deep interest and understanding of medical science• Excellent communication, presentation, and facilitation skills• Strong collaboration and influencing capabilities• Fluency in spoken and written EnglishAbout the OrganizationAstraZeneca Pharma India Ltd. is a global, science-led biopharmaceutical company focused on redefining disease management and improving patient outcomes through innovation, collaboration, and evidence-based medicine, with a strong presence in oncology and chronic disease care.

Role & Responsibilities• Build, develop, and maintain scientific engagement with Key External Experts (KEEs) and HCPs• Share emerging scientific data in an objective, balanced, and non-promotional manner• Provide insights on local clinical practice trends, unmet needs, and gaps in scientific knowledge• Develop scientifically based relationships across Gulf markets aligned with Medical Affairs strategy• Support scientific activities including clinical trials, NIS, ISS, and scientific exchange initiatives• Identify, train, and support speakers for local scientific meetings and advisory boards• Present scientific data in group settings and one-to-one HCP interactions• Facilitate CME activities and medically led meetings• Generate actionable insights to enhance disease management and appropriate product use• Support product launches through planning and execution of regional medical activities• Act as scientific expert for the respiratory/biologics disease area for internal stakeholders• Provide medical training and scientific updates to sales and internal teams• Respond to unsolicited medical information requests in compliance with policies and regulations• Ensure accurate documentation and adherence to ethical, legal, and company standardsQualification• Any graduation with strong medical/scientific background• Medical background training relevant to pharmaceutical Medical AffairsExperience• 1–3 years of experience preferred• Minimum 1 year experience in Medical Affairs within the pharmaceutical industry in Saudi Arabia• Mandatory experience in Respiratory/Biologics therapy area• Strong understanding of the Saudi healthcare environment and medical communitySkills• Expertise in respiratory/biologics scientific communication• Strong stakeholder engagement and KEE management skills• Excellent presentation and scientific storytelling abilities• Ability to synthesise complex scientific data for HCP audiences• Strong project management and planning skills• Excellent written and verbal communication skills• High level of independence, leadership, and professionalism• Proficiency in MS Excel, Word, and PowerPointAbout the Company• AstraZeneca Pharma India Ltd. is a leading global biopharmaceutical organisation, Focuses on innovative therapies across Respiratory, Oncology, Cardiovascular, Renal, and Biologics.

Role & Responsibilities• Represent AbbVie Medical Affairs as a subject matter expert in Oncology within the assigned territory• Build and maintain credible, professional scientific relationships with key opinion leaders (KOLs) and healthcare professionals• Serve as the primary medical point of contact for external experts within the assigned geography• Develop and execute scientific engagement plans and cycle plans aligned with medical strategy• Perform KOL tiering and segmentation and document interactions and insights in Veeva CRM• Maintain a strong medical and scientific presence at key academic and oncology centers• Provide scientific support and education to internal sales, marketing, and brand teams• Support medical projects and Global Medical Affairs (GMA) studies including registries, epidemiological and post-marketing studies• Support prioritized interventional clinical studies in collaboration with Clinical Development Operations• Facilitate investigator-initiated study (IIS) concepts and support requests in coordination with local and global medical teams• Deliver high-quality scientific presentations to physicians and expert groups• Attend scientific congresses and oncology conferences and share strategic insights internally• Support named patient and compassionate use requests in compliance with regulations• Ensure all activities comply with local laws, regulatory requirements, SOPs, and AbbVie R&D standardsQualification• MBBS and MD (preferred)• Candidates with relevant undergraduate degrees and appropriate experience will also be consideredExperience• 1–2 years of experience in Oncology Medical Affairs• Hemato-oncology experience preferred• Experience in clinical research and scientific engagement is desirableSkills• Strong scientific knowledge in oncology and clinical research methodologies• Solid understanding of pharmaceutical Medical Affairs function• Excellent written, verbal, and presentation skills• Strong stakeholder engagement and relationship-building ability• High ethical standards and strong compliance mindset• Ability to quickly learn new therapeutic areas and environmentsAbout The Company• AbbVie is a global biopharmaceutical company focused on delivering innovative medicines, Strong presence in oncology, immunology, neuroscience, and specialty care, Driven by science, ethics, and patient-centric innovation.

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.

Roles & Responsibilities• Perform end-to-end clinical data management activities for assigned studies• Review and evaluate clinical trial imaging and clinical data for accuracy and compliance• Collaborate with project teams to define study-specific edit checks• Run, review, and resolve data queries and discrepancies• Support study setup including database structure, specifications, and TF design• Coordinate receipt, integration, and processing of external and electronic clinical data• Maintain complete, accurate, and audit-ready study documentation• Track open data issues and ensure timely resolution• Ensure CDM activities comply with regulatory guidelines and internal SOPs• Participate in client meetings and cross-functional discussions• Continuously enhance technical and industry knowledge through trainingQualification• Bachelor’s degree in Life Sciences, Computer Science, or a related discipline• Equivalent clinical data management experience will be consideredExperience• Minimum 1 year of experience in Clinical Data Management (Pharma, Biotech, or CRO)Skills• Strong understanding of clinical trial terminology and CDM processes• Working knowledge of relational databases and data validation• SAS knowledge is desirable• Proficiency in MS Word, Excel, and Access• Strong analytical skills with high attention to detail• Excellent documentation, organizational, and communication skills• Ability to work independently and effectively in fast-paced team environmentsAbout the OrganisationClario is a global leader in clinical trial endpoint technology, delivering innovative imaging, cardiac safety, and digital endpoint solutions to support clinical trials worldwide. The company partners with leading pharmaceutical, biotech, and medical device organizations, offering professionals exposure to global studies, advanced technology platforms, and diverse therapeutic areas.

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.