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clinical liaison

Pfizer

<div>Job Description:
<ul><li>Medical Science Liaison (MSL) is a field &ndash;based medical function where 90% of his/ her time allocated is spent in the field in the respective territory.</li><li>The Medical Scientific Liaison (MSL) provides scientific expertise, build knowledge and activity-based relationships with Key Opinion Leaders to advance medical practice and research.</li><li>MSL role will act as a critical interface with identified scientific leaders and will build regional, national or international relationships to contribute to understanding of diseases, research and scientific trends, clinical practice, treatment patterns in the relevant therapeutic areas.</li></ul>
Main Responsibilities and Duties:<ul><li>To provide medical and scientific information to healthcare professionals in response to their specific requests for Pfizer to present clinical data about marketed products and reactively important scientific information on new products, or those in development</li><li>To develop and maintain medical and scientific partnerships with healthcare professionals.</li><li>To provide geographical focus and customer knowledge and insights, as members of Medical and Scientific Affairs team, to the development of the in-country medical plans and to feed into above-country and global medical plans.</li><li>To develop and maintain ongoing cross-functional working relationships with Pfizer colleagues in alignment with Pfizer SOPs</li></ul>
Requirements<ul><li>Advanced degree (PharmD, PhD, MD) in a relevant field with 1-2 years of experience in pharmaceutical or biotechnology industry.</li><li>Strong scientific and clinical knowledge in vaccinology and/or public health is a plus.</li><li>Excellent communication and presentation skills.</li><li>Ability to interpret and present complex scientific data.</li><li>Experience in developing and maintaining professional relationships with healthcare professionals.</li><li>Ability to work independently and as part of a team.</li><li>Willingness to travel as required (50% of time).</li><li>Knowledge of regulatory and compliance requirements.</li><li>Strong analytical and problem-solving skills.</li><li>Excellent interpersonal and networking skills.</li></ul>
The MSL reports to the in-country Primary &amp; Specialty Care Lead 
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical</div>

Medical Science Liaison

AstraZeneca

<div>Medical Scientific Liaison &ndash; V&amp;I 
ABOUT ASTRAZENECA
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world&rsquo;s most serious diseases. But we&rsquo;re more than one of the world&rsquo;s leading pharmaceutical companies.
Join a high-performing team, empowered to cut through the noise and drive real change. Our agility and pace, coupled with scientific focus, powers us to spot opportunities in the market that keep us moving forward and into new spaces.
SITE DESCRIPTION
AstraZeneca is experiencing a significant transformation in the Kingdom of Saudi Arabia, driven by a commitment to advancing healthcare, innovation, and sustainable growth. Building on our global legacy, AZ KSA is rapidly evolving its operations to better serve patients, collaborate with healthcare stakeholders, and contribute to the ambitious goals outlined in the Saudi Vision 2030. We are investing in talent, digital solutions, and new ways of working; all designed to enhance our impact on patient outcomes and reinforce our leadership in therapeutic areas. This dynamic environment calls for visionary, agile professionals who thrive in change and are motivated to help shape the future of healthcare in KSA.<div></div><div>
ROLE SUMMARY<div>
Medical Science Liaison (MSL) possesses extensive scientific expertise in respective therapeutic area and engages in scientific discussions and presentations with KEEs about the disease area, and clinical data in a non-promotional context.
This role is accountable for generating actionable insights from KEEs and communicating these to the brand team to shape the Medical and Brand strategy.
This role is responsible for a highly strategic product and disease area that involves working extensively with external stakeholders to forge strong relations and foster scientific and strategic partnerships within major hospitals and institutions/ authorities in their assigned territory and non-traditional stakeholders (E.g. policy and decision makers, payer groups, government, researchers, and others to help bridge the gaps and provide health system solutions.
This is a field-based Medical Affairs role requiring travel across assigned territories in Saudi Arabia to engage with healthcare professionals, external experts, institutions, and vaccination-related stakeholders.</div><div></div>
What you&rsquo;ll do<div>
Build, enhance, maintain advocacy of Key External Experts (KEEs)
<ul><li>Identify, prioritize, and expand KEEs to include non-traditional stakeholders (E.g. policy and decision makers, payer groups, government, researchers, and others) based on scientific/clinical expertise and practice change influence within a specific hospital and institution/ authorities, and engage in robust scientific discussions and medical advancements in a balanced, objective, and accurate way.</li><li>
Identify, and prioritize accounts based on patient care pathway and map the multidisciplinary team and maturity.</li><li>
Provide AZ with an understanding of the local medical community, clinical practice trends, HCP insight and real or perceived gaps in current scientific knowledge, patient journey, and disease management.</li><li>
Foster scientific partnerships with KEEs to help advance disease understanding and to achieve evidence-based changes in medical practice that are consistent with Medical Affairs strategy &amp; objectives, such as:
Interact in the field with the medical community in the context of various medical projects such as clinical trials, Non-Interventional Studies, Investigator Sponsored Studies (ISSs), scientific exchange.
 Identify potential speakers and train speakers as appropriate for local events.
Provide recommendations for advisory board / round table discussion participants and serve as faculty/facilitators for advisory board meetings.
Present scientific data to HCPs in both group (Medically led meetings) and one on one setting.
Facilitate continuing medical education events for HCPs.
Support evidence generation in the region aligned with the medical strategy of disease area and product.</li></ul>
Build and implement scientific programs to address unmet medical needs in priority disease area(s)
<ul><li>Collect and share actionable insights that enhance the value and appropriate use of AZ products and disease management to internal stakeholders.</li><li>
Engage in strategic planning meetings and medical-scientific presentations with medication access stakeholders, institutional decision makers and other external stakeholders to drive better clinical decisions and enhance medication accessibility within the assigned hospital or institution. These discussions are scientific in nature and must be clearly separated from promotional and/ or other business discussions.</li><li>
Organize and facilitate scientific events on healthcare institutions and their multi-disciplinary teams related to the therapeutic area to ensure holistic approach to patient care within their hospital and institution.</li><li>
Embed a comprehensive healthcare system and patient experience understanding in prioritized hospitals and institutions to transform care and improve patient outcomes.</li></ul>
Act as scientific expert in priority disease area for internal stakeholders.<ul><li>
Demonstrate expertise and knowledge of AZ products, emerging therapies, competitors, patient and treatment trends, clinical trials, and scientific activities within the disease area and continuously updates this expertise and knowledge.</li><li>
Provide the AZ internal stakeholders with an understanding of the local medical community, clinical practice, trends and real or perceived gaps in current scientific knowledge and medical treatment options/ guidelines through periodic therapeutic area and product trainings.</li><li>
Provide scientific support at AZ sponsored educational events.</li><li>
Plan and execute regional medical activities during the product launch processes.</li></ul>
Medical Information<ul><li>
Respond to unsolicited requests for information about unapproved AZ products or unapproved uses of approved products, presenting such information in an objective, well balanced, substantiated manner that is scientific in tone and content, free of promotional messages, truthful, and is not misleading.</li><li>
Demonstrate appropriate response and documents the provision of accurate, scientific data in response to unsolicited scientific questions posed by healthcare providers with Company Policies, and applicable laws, regulations, and ethical standards.</li></ul>
Only Applications in KSA will be considered.
Essential for the role
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be.
Essential Capabilities:<ul><li>
Experience with the healthcare environment and related dynamics in Saudi Arabia is necessary.</li><li>
Experience in Vaccines / infectious diseases therapy area is a plus.</li><li>
Minimum of 2 years of experience in the pharmaceutical industry in Saudi Arabia, with exposure to scientific activities</li><li>
Experience or exposure to vaccines, infectious diseases, public health initiatives.</li><li>
Experience with the healthcare environment, including opinion leaders, the medical community, and related dynamics in Saudi Arabia, is must.</li><li>
An established track record of driving clinical practice shaping and impactful stakeholder mobilization.</li></ul>
Desirable Capabilities:<ul><li>
Demonstrated business acumen and track record of end -to-end project management.</li><li>
Full understanding of the medical role in driving innovative value strategies and supporting patient access to evidence-based treatment is an advance.</li><li>
Established track record of basic or clinical research.</li><li>
Prior experience in vaccines, infectious diseases, public health, immunization programs, national scientific committees is preferred.</li></ul>
Why AstraZeneca?
At AstraZeneca we&rsquo;re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There&rsquo;s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We&rsquo;re on an exciting journey to pioneer the future of healthcare. 
So, what&rsquo;s next?
<ul><li>Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.</li><li>
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it&rsquo;s yours.</li></ul>
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram</div></div></div>

Medical Scientific Liaison - V&I

<div>Site Name: Jeddah Headquarters Business Park, Riyadh Olaya Towers 
Posted Date: Apr 28 2026 
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients&rsquo; needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it&rsquo;s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Haemato-Oncology Medical Scientific Liaison 
You will be a field-based Haemato-Oncology Medical Scientific Liaison supporting medical engagement across Saudi Arabia. You will build trusted, scientific relationships with haematology and oncology experts. You will gather and share medical insights to shape evidence generation and medical strategy. We value clear communicators who work well across teams and who are motivated by making a real difference for patients. This role offers growth through exposure to clinical development, cross-functional projects, and opportunities to influence care in line with GSK&rsquo;s mission to unite science, technology and talent to get ahead of disease together. The Medical Scientific Liaison (MSL) is a non-promotional field-based medical role responsible for conducting medical engagements/activities that ensure the safe and effective use of GSK&rsquo;s medicines while generating medical insights. MSL is expected to drive EEs/HCPs education journeys using the behavior adoption tool, provide support to GSK clinical development &amp; Key Evidence Generation programs.
Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<ul><li>Conduct peer-to-peer scientific interactions with haemato and oncology healthcare professionals, both proactively and reactively.</li><li>Capture, document and share medical insights to inform local evidence generation and medical strategy.</li><li>Support medical education activities, advisory boards, and scientific workshops for external experts and internal colleagues.</li><li>Provide timely, fair and evidence-based responses to unsolicited medical information requests and safety queries.</li><li>Support clinical development activities such as investigator identification and site feasibility when required.</li><li>Use approved systems to record activities and outcomes, and ensure compliance with local laws, policies and pharmacovigilance requirements.</li></ul>
Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:<ul><li>Bachelor&rsquo;s degree in pharmaceutical science.</li><li>Saudi National</li><li>Valid license from the Saudi Commission for Health Specialties or equivalent local licensure.</li><li>At least 2 years&rsquo; experience in pharmaceutical medical, clinical, or field roles.</li><li>Practical knowledge of haemato-oncology clinical practice or experience working with oncology or haematology healthcare professionals.</li><li>Strong written and spoken English. Arabic is an advantage.</li><li>Excellent communication skills and experience presenting clinical data to healthcare audiences.</li></ul>
Preferred Qualification
If you have the following characteristics, it would be a plus<ul><li>Advanced degree ( PhD, or MSc) or postgraduate training in hematology, oncology, or related area.</li><li>Experience supporting clinical trials, investigator identification, or site engagement.</li><li>Familiarity with medical information systems and CRM platforms.</li><li>Experience in evidence generation, publications, or health economics and outcomes research.</li><li>Experience working within a matrix environment and collaborating with commercial, access, and regulatory teams.</li><li>Fluency in Arabic and experience engaging national stakeholders, payers or guideline committees.</li></ul>
Work Model
This role will be based in Saudi Arabia and is field-based with regular travel across the assigned geography. The role is on-site and hybrid working arrangements may be agreed based on business needs and local policy.
How to apply
If this role speaks to your skills and goals, we encourage you to apply. Tell us how your experience in haemato-oncology and scientific engagement will help patients and teams succeed. We look forward to hearing from you. #LI-Remote
نقوم بتصنيع وتوريد أدوية ولقاحات موثوقة وعالية الجودة لتلبية احتياجات المرضى وتعزيز أدائنا. سلَّمت شبكتنا المكوّنة من 37 موقعًا لإنتاج الأدوية واللقاحات ما مجموعه 1.7 مليار عبوة أدوية و409 مليون جرعة لقاح في عام 2024، مساهمةً في تحقيق أثر إيجابي على صحة ملايين الأشخاص. سلسلة التوريد لدينا ليست مجرد عنصر أساسي في عملياتنا؛ بل هي حيوية لإيصال ابتكاراتنا إلى المرضى بأسرع شكل ممكن وبكفاءة وفاعلية. تعمل التكنولوجيا على تحويل طريقة تصنيع الأدوية واللقاحات، مما يتيح لنا زيادة سرعة وجودة وحجم التوريد. نحتاج أفضل العقول والقدرات لمساندتنا في رحلتنا نحو تصنيع منتجات أكثر تعقيدًا، مستفيدين من قوة تقنيات التصنيع الذكي بما في ذلك الروبوتات، والحلول الرقمية، والذكاء الاصطناعي لخدمة المرضى.
منسق علمي طبي &mdash; أمراض الدم والأورام (Haemato‑Oncology Medical Scientific Liaison)
ستكون منسقًا علميًا طبيًا ميدانيًا في مجال أمراض الدم والأورام، تدعم التواصل الطبي عبر المملكة العربية السعودية. ستبني علاقات علمية موثوقة مع خبراء أمراض الدم والأورام، وستجمع وتشارك الرؤى الطبية للمساهمة في تشكيل جهود توليد الأدلة والاستراتيجية الطبية. نُقدّر أصحاب التواصل الواضح الذين يعملون بفاعلية عبر الفرق والذين يتحفّزون لإحداث فرق حقيقي للمرضى. يوفر هذا الدور فرصًا للنمو من خلال التعرض لتطوير الدراسات السريرية، المشاريع متعددة التخصصات، وفرص التأثير على الرعاية بما يتماشى مع مهمة GSK في توحيد العلم والتكنولوجيا والمواهب للتقدّم على الأمراض معًا.
المسؤوليات
يوفر هذا الدور لك الفرصة لقيادة أنشطة رئيسية لتطوير مسارك المهني. تشمل بعض المسؤوليات ما يلي:<ul><li>
إجراء تفاعلات علمية بين النظراء مع مختصي أمراض الدم والأورام، بشكل استباقي واستجابي.</li><li>
جمع وتوثيق ومشاركة الرؤى الطبية لإثراء جهود توليد الأدلة المحلية والاستراتيجية الطبية.</li><li>
دعم أنشطة التعليم الطبي، مجالس الاستشارة (advisory boards)، وورش العمل العلمية للخبراء الخارجيين والزملاء الداخليين.</li><li>
تقديم ردود مبنية على الأدلة وفي الوقت المناسب على طلبات المعلومات الطبية غير الموجّهة واستفسارات السلامة.</li><li>
دعم أنشطة التطوير السريري مثل تحديد المحققين ودراسة جدوى المواقع عند الحاجة.</li><li>
استخدام الأنظمة المعتمدة لتسجيل الأنشطة والنتائج، وضمان الامتثال للقوانين المحلية والسياسات ومتطلبات اليقظة الدوائية (Pharmacovigilance).</li></ul>
لماذا أنت؟
المؤهلات الأساسية نبحث عن محترفين يمتلكون المهارات والمؤهلات التالية لمساعدتنا في تحقيق أهدافنا:<ul><li>
الصيدلة.</li><li>
ترخيص ساري من الهيئة السعودية للتخصصات الصحية.</li><li>
خبرة لا تقل عن سنتين في أدوار طبية أو سريرية أو ميدانية في قطاع الأدوية.</li><li>
معرفة عملية بممارسات الرعاية السريرية في أمراض الدم والأورام أو خبرة في العمل مع مختصي الأورام أو أمراض الدم.</li><li>
إجادة قوية للغة الإنجليزية كتابةً ومحادثة؛ تُعتبر اللغة العربية ميزة.</li><li>
مهارات تواصل ممتازة وخبرة في عرض البيانات السريرية أمام جمهور من المتخصصين في الرعاية الصحية.</li></ul>
المؤهلات المفضلة
إن توافرت لديك الخصائص التالية فستكون ميزة:<ul><li>
شهادة متقدمة أو تدريب متخصص في أمراض الدم أو الأورام أو مجال ذي صلة.</li><li>
خبرة في دعم التجارب السريرية، تحديد المحققين أو التواصل مع مواقع البحث.</li><li>
إلمام بأنظمة المعلومات الطبية ومنصات إدارة علاقات العملاء (CRM).</li><li>
خبرة في توليد الأدلة، النشر العلمي، أو أبحاث اقتصاديات الصحة ونتائج الرعاية.</li><li>
خبرة العمل ضمن بيئة مصفوفية والتعاون مع فرق تجارية، فرق الوصول (access) والجهات التنظيمية.</li><li>
إجادة اللغة العربية وخبرة في التواصل مع أصحاب المصلحة الوطنيين أو دافعي التكلفة أو لجان وضع الإرشادات.</li></ul>
نموذج العمل
سيكون هذا الدور ميدانيًا ومقرّه المملكة العربية السعودية، ويتطلب سفرًا منتظمًا ضمن المنطقة المخصصة. الدور يتطلب تواجدًا ميدانيًا، ويمكن الاتفاق على ترتيبات عمل هجينة حسب احتياجات العمل والسياسة المحلية.
كيفية التقديم
إذا كان هذا الدور يتوافق مع مهاراتك وأهدافك، نشجعك على التقديم. أخبرنا كيف ستسهم خبرتك في أمراض الدم والأورام والتواصل العلمي في دعم المرضى والفرق على النجاح. نتطلع لسماعك. #LI-Remote
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Haemato-Oncology Medical Scientific Liaison (MSL)

<div>Site Name: Riyadh Olaya Towers 
Posted Date: Apr 23 2026 
<div><div>
GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.
</div></div>Job Purpose:<ul><li>
The Medical Scientific Liaison (MSL) is a non-promotional field-based medical role responsible for conducting medical engagements/activities that ensure the safe and effective use of GSK&rsquo;s medicines while generating medical insights.</li><li>
MSLs are expected to drive EEs/HCPs education journeys using the Sc/AUBB+ tool, provide support to GSK clinical development &amp; Key Evidence Generation programs.</li></ul>
Key Responsibilities:<ul><li>
Provide product and disease area information to external experts. This need is met primarily through direct scientific interactions with external experts and healthcare professionals, including proactive data presentations and reactive responses to medical information queries.</li></ul><ul><li>
MSLs are field-based scientific experts in specific therapeutic areas, clinical practice, and competitor landscape. Through his/her expertise and external interactions he/she will gather insights which will assist in the development and execution of innovative Medical Affairs strategies and plans that clearly support GSK development of medicines of value for patients.</li></ul><ul><li>
The language and activities of the MSL must always reflect the medical nature of the role, be fair, balanced, scientific and evidence based. MSLs may be required to manage scientific engagement budget, train internal stakeholders and contribute in medical affairs and/or R&amp;D activities.</li></ul>
MSLs responsibilities include:
Collect &amp; generate insights:
<ul><li>Conduct proactive/reactive (1:1), (1: many) discussions and meetings, support advisory boards/consultations and scientific workshops.</li><li>
Use GSK tools to capture insights and medical voice of customers while regularly assessing related KPIs and their impact on TA strategic objectives</li><li>
Attend scientific meetings/congresses</li></ul>
Inform decisions:
<ul><li>Provide product and TA information to internal and External customers.</li><li>
Conduct Medical Education programs. (GSK led, collaborative or supported)</li><li>
Map evidence gaps &amp; collaborate in developing evidence generation plans</li><li>
Support patients access to GSK brands</li><li>
Engage &amp; represent medical with EE, payers, government &amp; formularies</li></ul>
Change behavior:<ul><li>
Work collaboratively to scale EE Sc/AUBB+ level in the assigned TA</li><li>
Engage proactively/reactively (according to Asset local registration status) to update TA related guidelines and educate HCPs about them</li><li>
Transform guidelines into execution protocols</li><li>
Address HCP&rsquo;s unsolicited questions regarding GSK products within the Medical Affairs/scientific/Medical Information booth</li></ul>
Evidence Generation and R&amp;D:<ul><li>
Identify local evidence gaps and propose EG initiatives</li><li>
Support EG int/ext approvals while factoring in budget requirements</li><li>
Work collaboratively with respective functions to drive local publications</li><li>
Identify opportunities to bring R&amp;D projects to LOC</li></ul>
Medical Governance:<ul><li>
Ensure on label external communication and document off-label reactive responses to MI queries as per relevant SOPs</li><li>
Ensure compliance with GSK policies, standards, and with local codes of practice, Saudi FDA regulations and laws.</li><li>
Act as a focal point of contact for relevant TA management monitoring, internal audits and/or inspections</li><li>
Timely execution of agreed audits &amp; inspections CAPAs</li><li>
Identify risks &amp; mitigation plans related to assigned TAs/ Med dep</li></ul>
Pharmacovigilance:<ul><li>
Ensure fulfillment of PV training requirements for self &amp; 3rd parties</li><li>
Ensure that PV requirements are reflected across int &amp; ext engagements</li><li>
Support PV audits and/or inspections within respective TAs</li><li>
Communicate up to date safety data to HCPs as part of fair &amp; balanced communication</li><li>
Ensure safety reporting responsibilities are met by self and others</li></ul>
Job Complexity:<ul><li>
The position requires (proficient) grade skills across communication, medical governance, value access and evidence generation capabilities.</li><li>
Comfortable working across boundaries in matrix organization across functions, geographies and cultures.</li><li>
Individual contributor with medium to high job complexity and a high level of autonomy &amp; accountability</li></ul>
Knowledge, Skills &amp; Competencies:<ul><li>
Pharmaceutical science degree (Saudi National)</li><li>
At least 2-year experience . Respiratory Therapy Area experience is preferred.</li><li>
Proven successful track record.</li><li>
Having a valid license from the Saudi Commission for Health Specialties</li><li>
Ability to analyze, present and discuss scientific data in the therapeutic area with external and internal stakeholders</li><li>
High level of discipline, ability to organize the activity and to reasonably use the working time within the established independence limits.</li><li>
Developed skills in business planning, business orientation and working under a dynamically changing condition</li><li>
Fluent in professional English language. Arabic language is an advantage.</li></ul>
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
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Medical Science Liaison - Respiratory

<div>JOB TITLE
 Medical Advisor &ndash; Respiratory 
 
ABOUT ASTRAZENECA
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world&rsquo;s most serious diseases. But we&rsquo;re more than one of the world&rsquo;s leading pharmaceutical companies.
SITE DESCRIPTION
AstraZeneca is experiencing a significant transformation in the Kingdom of Saudi Arabia, driven by a commitment to advancing healthcare, innovation, and sustainable growth. Building on our global legacy, AZ KSA is rapidly evolving its operations to better serve patients, collaborate with healthcare stakeholders, and contribute to the ambitious goals outlined in the Saudi Vision 2030. We are investing in talent, digital solutions, and new ways of working; all designed to enhance our impact on patient outcomes and reinforce our leadership in therapeutic areas. This dynamic environment calls for visionary, agile professionals who thrive in change and are motivated to help shape the future of healthcare in KSA.
ROLE SUMMARY
AstraZeneca is pioneering the next generation of respiratory care, leveraging our deep heritage and a robust portfolio to transform the lives of patients with chronic airway diseases. This high-impact therapy area addresses significant unmet medical needs across asthma and COPD, spanning both inhaled therapies and advanced biologic treatments.
The Medical Advisor &ndash; Respiratory role ensures the delivery of high-quality and impactful scientific engagement, medical education, evidence support, and insight generation in alignment with respiratory TA priorities. The role is also responsible for driving the execution of medical activities and building advocacy with relevant specialties across the Central Region of Saudi Arabia. You will act as a trusted scientific partner to healthcare professionals, multidisciplinary teams, and centres of excellence, ensuring that science, clinical precision, and patient outcomes remain at the core of every initiative.
This role requires strong therapeutic knowledge in respiratory diseases, scientific acumen, and the ability to connect field-based insights to broader medical and business strategies during a critical phase of portfolio growth and new launches.
The role may take responsibility as reviewer for activities and promotional materials and may lead Medical Information and Pharmacovigilance within a particular market.
What you&rsquo;ll do
Field Medical Excellence<ul><li>
Execute the Respiratory Medical Affairs Plan in alignment with TA leadership and cross-functional teams.</li><li>
Deliver high-quality scientific exchange with HCPs and decision-makers to support the appropriate use of asthma and COPD therapies.</li><li>
Drive disease education initiatives, multidisciplinary collaborations, and patient identification strategies across asthma and COPD.</li><li>
Support launch readiness and lifecycle management activities across the respiratory portfolio.</li></ul>
Scientific Engagement and External Collaboration<ul><li>
Build strong peer-to-peer relationships with Key External Experts (KEEs) across pulmonology, allergy/immunology, and related specialties.</li><li>
Lead and contribute to scientific meetings, advisory boards, and symposia as a subject-matter expert in respiratory diseases.</li><li>
Support speaker development, CME activities, and scientific partnerships aligned with the respiratory strategy.</li><li>
Generate and communicate actionable insights to inform local strategy and identify opportunities to improve patient care and access.</li></ul>
Evidence Generation and Data Dissemination<ul><li>
Support local studies, registries, and Investigator-Initiated Studies (IIS) across asthma and COPD.</li><li>
Contribute to the development and review of scientific materials ensuring accuracy and compliance.</li><li>
Disseminate emerging clinical and real-world evidence on respiratory therapies in an ethical and balanced manner.</li></ul>
Cross-Functional Medical Support<ul><li>
Partner with Market Access, HEOR, Commercial, and Regulatory teams to ensure strong scientific alignment.</li><li>
Provide medical input into formulary discussions, value communication, and payer engagement.</li><li>
Deliver scientific training and support to internal stakeholders across the respiratory portfolio.</li></ul>
Compliance and Medical Governance<ul><li>
Ensure all activities align with AstraZeneca&rsquo;s ethical standards, SOPs, and SFDA regulations.</li><li>
Maintain full compliance in documentation, adverse event reporting, and insight capture systems.</li></ul>
Only applications in KSA will be considered.
Essential for the role<ul><li>
Bachelor&rsquo;s degree in medicine or pharmacy is required</li><li>
Post-graduate master&rsquo;s degree is an advantage</li><li>
Respiratory experience is a must.</li><li>
2+ years of experience in Medical Affairs, preferably in respiratory (asthma/COPD).</li><li>
Experience across inhaled therapies and/or biologics is strongly preferred.</li><li>
Understanding of patient pathways, referral systems, and access dynamics in respiratory care within Saudi Arabia.</li><li>
Ability to translate complex scientific data into meaningful clinical value.</li><li>
Strong strategic thinking with solid business and healthcare system understanding.</li></ul>
Desirable for the role<ul><li>
Knowledge of company products and allocated therapeutic areas, expertise at relevant therapy area</li><li>
Acts independently, is willing to take on challenges, and can say no to stakeholders when necessary</li><li>
Sets high standards of work and makes others accountable for achieving outstanding performance</li></ul>
Why AstraZeneca?
At AstraZeneca we&rsquo;re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There&rsquo;s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We&rsquo;re on an exciting journey to pioneer the future of healthcare. 
So, what&rsquo;s next?
<ul><li>Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.</li><li>
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it&rsquo;s yours.</li></ul>
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram</div>

Medical Advisor – Respiratory

Novartis

<div>
 
 Summary
 
 
 
 To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis&rsquo; compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders&rsquo; scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.
 
 
 
 About The Role
 
 
 
 
 Medical Expert Engagement
 
 
 
 <ul>
 <li>
 Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).
 </li>
 <li>
 Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.
 
 
 </li>
 </ul>
 
 Scientific Information &amp; Requests
 
 
 
 <ul>
 <li>
 Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.
 </li>
 <li>
 Involve HCPs in advisory boards, educational activities, and publications when relevant.
 
 
 </li>
 </ul>
 
 Clinical Research Support
 
 
 
 <ul>
 <li>
 Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.
 </li>
 <li>
 Facilitate IIT submissions and material transfer agreements for independent research.
 
 
 </li>
 </ul>
 
 Scientific Exchange &amp; Insights
 
 
 
 <ul>
 <li>
 Promote scientific exchange on emerging principles and trends.
 </li>
 <li>
 Collect and report HCP insights to inform medical strategy and IPS planning.
 
 
 </li>
 </ul>
 
 Internal Contributions
 
 
 
 <ul>
 <li>
 Act as a local medical resource for disease area and product training.
 </li>
 <li>
 Contribute to IPS and Medical Affairs strategy design and execution.
 
 
 </li>
 </ul>
 
 Compliance &amp; Integrity
 
 
 
 <ul>
 <li>
 Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).
 </li>
 <li>
 Foster a diverse, inclusive, and harassment-free environment.
 
 
 </li>
 </ul>
 
 Education &amp; Communication
 
 
 
 <ul>
 <li>
 Provide scientific and educational information to HCPs on patient-critical issues.
 </li>
 <li>
 Support internal capability building through training and knowledge sharing.
 
 
 </li>
 </ul>
 
 Minimum Requirements
 
 
 
 <ul>
 <li>
 A degree in PharmD, PhD, MD (Medical Doctor) is essential.
 </li>
 <li>
 At least 1-year experience as Medical Science Liaison, specific experience in Hematology is a plus.
 </li>
 <li>
 Fluent in both Arabic and English languages.
 
 
 </li>
 </ul>
 
 Why Novartis:
 
 Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
 
 
 
 Benefits and Rewards:
 
 Learn about all the ways we&rsquo;ll help you thrive personally and professionally.
 
 
 Read our handbook (PDF 30 MB)
 
 
</div>

Senior Hematology Medical Science Liaison - Riyadh

<div><div><h3 class="jobSectionHeader">Summary
</h3><div>To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis&rsquo; compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders&rsquo; scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate. 
 
#LI-Onsite</div>
</div><div><h3 class="jobSectionHeader">About the Role
</h3><div><h3 class="jobSectionHeader">Medical Expert Engagement</h3><ul><li>
Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).</li><li>
Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.</li></ul><h3 class="jobSectionHeader">
Scientific Information &amp; Requests</h3><ul><li>
Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.</li><li>
Involve HCPs in advisory boards, educational activities, and publications when relevant.</li></ul><h3 class="jobSectionHeader">
Clinical Research Support</h3><ul><li>
Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.</li><li>
Facilitate IIT submissions and material transfer agreements for independent research.</li></ul><h3 class="jobSectionHeader">
Scientific Exchange &amp; Insights</h3><ul><li>
Promote scientific exchange on emerging principles and trends.</li><li>
Collect and report HCP insights to inform medical strategy and IPS planning.</li></ul><h3 class="jobSectionHeader">
Internal Contributions</h3><ul><li>
Act as a local medical resource for disease area and product training.</li><li>
Contribute to IPS and Medical Affairs strategy design and execution.</li></ul><h3 class="jobSectionHeader">
Compliance &amp; Integrity</h3><ul><li>
Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).</li><li>
Foster a diverse, inclusive, and harassment-free environment.</li></ul><h3 class="jobSectionHeader">
Education &amp; Communication</h3><ul><li>
Provide scientific and educational information to HCPs on patient-critical issues.</li><li>
Support internal capability building through training and knowledge sharing.</li></ul>
Minimum Requirements<ul><li>
A degree in PharmD, PhD, MD (Medical Doctor) is essential.</li><li>
At least 1-year experience as Medical Science Liaison, specific experience in Hematology is a plus.</li><li>
Fluent in both Arabic and English languages.</li></ul></div>
</div><div><div>Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Learn about all the ways we&rsquo;ll help you thrive personally and professionally. 
Read our handbook (PDF 30 MB)</div></div></div>
 <div><div>Division
<div>International
</div></div><div>Business Unit
<div>Development
</div></div><div>Location
<div>Saudi Arabia
</div></div><div>Site
<div>Riyadh
</div></div><div>Company / Legal Entity
<div>SA01 (FCRS = SA001) Novartis Saudi Arabia Ltd
</div></div><div>Alternative Location 1
<div>Jeddah, Saudi Arabia
</div></div><div>Functional Area
<div>Research &amp; Development
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No</div></div></div><div></div>

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