msl rare disease

AstraZeneca

<div>JOB TITLE
 Medical Science Liaison &ndash; Rare Diseases (Hematology, Nephrology and Transplant)
 Location: Riyadh 
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 accelerating the expansion of our geographical footprint in rare diseases following the acquisition of Alexion in 2021. Rare disease is a high-growth therapy area with rapid innovation and significant unmet medical need. Over 7,000 rare diseases are known today &ndash; yet less than 1% of them have an approved treatment.
As we build our position as a Rare Disease leader, we seek a Rare Disease Medical Science Liaison to join our Medical Affairs team in Central/Eastern Regions, KSA.
As a Medical Science Liaison &ndash; Rare Disease you'll play a pivotal role in channelling our scientific capabilities to bring an important new therapy in a rare disease setting into clinical practice, making a positive impact on patients' lives.
The Medical Science Liaison &ndash; Rare Disease is a professional with scientific, clinical and therapeutic area expertise responsible for providing medical and scientific support to healthcare professionals aligned to the use of medicines in our combined rare disease portfolio. You will report into the Medical Manager Rare Disease.
In this role you will be expected to identify and cultivate relationships with HCPs working in the field including physicians, nurse practitioners, registered nurses and pharmacists as well as other key strategic partners, such as patient advocacy groups. You will conduct educational programs on disease state and the appropriate use of our medicines, consistent with Medical Affairs plans and objectives. You will also respond to customer inquiries to ensure focused clinical and scientific information that supports the appropriate use of these medicines.
Additionally you will deliver clinical and scientific information to support appropriate use of the medicine in the relevant therapy area in a patient focused manner; maintain expertise in disease state management, keep abreast of emerging therapies and the therapeutic landscape; gather customer insights regarding the use of the medicine in the wider therapeutic landscape to help inform medical and commercial strategies while adhering to internal standards, processes and complying with regulatory and compliance requirements.
What you&rsquo;ll do
Build, enhance, maintain the engagement with scientific leaders (KEEs)<ul><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 and medical treatment</li><li>
Share emerging data with HCPs, discussing all aspects of the data in a scientific, objective, and balanced way.
</li><li>Responsible for identifying and developing scientifically based relationships with KEEs in Gulf markets.</li><li>
Work with HCPs as partners in scientific activities that help advance disease understanding and are consistent with Medical Affairs strategy &amp; objectives, such as:<ul><li>
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.</li><li>
 Identify potential speakers and train speakers as appropriate for local events</li><li>
Provide recommendations for advisory board/Round Table discussion participants and serve as faculty/facilitators for advisory board meetings.</li><li>
Present scientific data to HCPs in both group (Medically led meetings) and one on one setting.</li><li>
Facilitate continuing medical education events for HCPs.</li></ul></li></ul>
Develop or initiate scientific programs to explore unmet medical needs in priority disease area(s) through obtaining and sharing valuable insights<ul><li>
Provide 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 with payer customers or hospital decision makers where the discussion of scientific topics is clearly separated from discussion of promotional and/or other business topics.</li><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 based on training direction and approved resources provided.</li><li>
Support the Medical Manager and Marketing Team in development of non-promotional and promotional materials/programs.</li></ul>
Act as scientific expert in priority disease area for internal stakeholders<ul><li>
Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds.</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, competitor information</li><li>
Provide scientific support at AZ sponsored educational events</li><li>
Gather, monitor, and share competitor knowledge that may affect company strategies</li><li>
Planning and executing regional medical activities during the product launch processes.</li></ul>
Medical Background Training<ul><li>
Serve as a medical resource for the sales representatives and accurately answer any medical question they may have to help them utilize their approved materials and to help them understand therapeutic area.</li><li>
Participate/develop/conduct therapeutic area and product trainings and periodic scientific updates to the internal customers</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 based in KSA will be considered.
Essential for the role<ul><li>
Bachelor&rsquo;s degree in medicine, Pharmacy, Pharmacology.</li><li>
Experience in rare disease therapeutic area</li><li>
2+ years of experience in the Pharmaceutical industry or equivalent</li><li>
Demonstrated expertise in synthesizing scientific information and communicating it effectively at peer level with HCPs.</li><li>
Excellent ability to learn and capacity for scientific concepts and knowledge.</li><li>
Previous experience in field medical role</li><li>
Experience in Hematology, oncology, Nephrology, rare diseases and/or critical care specialties are highly regarded.</li><li>
Direct patient care experience or equivalent experience in the pharmaceutical industry</li><li>
Strong presentation skills - effectively communicating medical data/concepts</li><li>
Excellent computer skills (Excel, Word, Power Point, etc.)</li><li>
Excellent project management ability</li><li>
Excellent oral and written communication and interpersonal skills</li><li>
Strong leadership capabilities with the ability to work independently</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>

MSL Rare Disease

<div>
 
 JOB TITLE
 
 
 
 
 Medical Science Liaison &ndash; Rare Diseases (Hematology, Nephrology and Transplant)
 
 
 
 
 Location: Riyadh
 
 
 
 
 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 accelerating the expansion of our geographical footprint in rare diseases following the acquisition of Alexion in 2021. Rare disease is a high-growth therapy area with rapid innovation and significant unmet medical need. Over 7,000 rare diseases are known today &ndash; yet less than 1% of them have an approved treatment.
 
 
 As we build our position as a Rare Disease leader, we seek a Rare Disease Medical Science Liaison to join our Medical Affairs team in Central/Eastern Regions, KSA.
 
 
 As a Medical Science Liaison &ndash; Rare Disease you'll play a pivotal role in channelling our scientific capabilities to bring an important new therapy in a rare disease setting into clinical practice, making a positive impact on patients' lives.
 
 
 The Medical Science Liaison &ndash; Rare Disease is a professional with scientific, clinical and therapeutic area expertise responsible for providing medical and scientific support to healthcare professionals aligned to the use of medicines in our combined rare disease portfolio. You will report into the Medical Manager Rare Disease.
 
 
 In this role you will be expected to identify and cultivate relationships with HCPs working in the field including physicians, nurse practitioners, registered nurses and pharmacists as well as other key strategic partners, such as patient advocacy groups. You will conduct educational programs on disease state and the appropriate use of our medicines, consistent with Medical Affairs plans and objectives. You will also respond to customer inquiries to ensure focused clinical and scientific information that supports the appropriate use of these medicines.
 
 
 Additionally you will deliver clinical and scientific information to support appropriate use of the medicine in the relevant therapy area in a patient focused manner; maintain expertise in disease state management, keep abreast of emerging therapies and the therapeutic landscape; gather customer insights regarding the use of the medicine in the wider therapeutic landscape to help inform medical and commercial strategies while adhering to internal standards, processes and complying with regulatory and compliance requirements.
 
 
 
 What You&rsquo;ll Do
 
 
 
 
 Build, enhance, maintain the engagement with scientific leaders (KEEs)
 
 
 
 <ul>
 <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 and medical treatment
 </li>
 <li>
 Share emerging data with HCPs, discussing all aspects of the data in a scientific, objective, and balanced way.
 </li>
 <li>
 Responsible for identifying and developing scientifically based relationships with KEEs in Gulf markets.
 </li>
 <li>
 Work with HCPs as partners in scientific activities that help advance disease understanding and are consistent with Medical Affairs strategy &amp; objectives, such as:
 </li>
 <ul>
 <li>
 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.
 </li>
 <li>
 Identify potential speakers and train speakers as appropriate for local events
 </li>
 <li>
 Provide recommendations for advisory board/Round Table discussion participants and serve as faculty/facilitators for advisory board meetings.
 </li>
 <li>
 Present scientific data to HCPs in both group (Medically led meetings) and one on one setting.
 </li>
 <li>
 Facilitate continuing medical education events for HCPs.
 
 </li>
 </ul>
 </ul>
 
 Develop or initiate scientific programs to explore unmet medical needs in priority disease area(s) through obtaining and sharing valuable insights
 
 
 
 <ul>
 <li>
 Provide 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 with payer customers or hospital decision makers where the discussion of scientific topics is clearly separated from discussion of promotional and/or other business topics.
 </li>
 <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 based on training direction and approved resources provided.
 </li>
 <li>
 Support the Medical Manager and Marketing Team in development of non-promotional and promotional materials/programs.
 
 
 </li>
 </ul>
 
 Act as scientific expert in priority disease area for internal stakeholders
 
 
 
 <ul>
 <li>
 Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds.
 </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, competitor information
 </li>
 <li>
 Provide scientific support at AZ sponsored educational events
 </li>
 <li>
 Gather, monitor, and share competitor knowledge that may affect company strategies
 </li>
 <li>
 Planning and executing regional medical activities during the product launch processes.
 
 
 </li>
 </ul>
 
 Medical Background Training
 
 
 
 <ul>
 <li>
 Serve as a medical resource for the sales representatives and accurately answer any medical question they may have to help them utilize their approved materials and to help them understand therapeutic area.
 </li>
 <li>
 Participate/develop/conduct therapeutic area and product trainings and periodic scientific updates to the internal customers
 
 
 </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 based in KSA will be considered.
 
 
 
 
 Essential For The Role
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in medicine, Pharmacy, Pharmacology.
 </li>
 <li>
 Experience in rare disease therapeutic area
 </li>
 <li>
 2+ years of experience in the Pharmaceutical industry or equivalent
 </li>
 <li>
 Demonstrated expertise in synthesizing scientific information and communicating it effectively at peer level with HCPs.
 </li>
 <li>
 Excellent ability to learn and capacity for scientific concepts and knowledge.
 </li>
 <li>
 Previous experience in field medical role
 </li>
 <li>
 Experience in Hematology, oncology, Nephrology, rare diseases and/or critical care specialties are highly regarded.
 </li>
 <li>
 Direct patient care experience or equivalent experience in the pharmaceutical industry
 </li>
 <li>
 Strong presentation skills - effectively communicating medical data/concepts
 </li>
 <li>
 Excellent computer skills (Excel, Word, Power Point, etc.)
 </li>
 <li>
 Excellent project management ability
 </li>
 <li>
 Excellent oral and written communication and interpersonal skills
 </li>
 <li>
 Strong leadership capabilities with the ability to work independently
 
 
 </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
 
 
 
 Date Posted
 
 
 
 22-Dec-2025
 
 
 
 Closing Date
 
 
 
 30-Dec-2025
 
 
 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. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
</div>

Ipsen

<div>
 <ul>
 <li>
 MSL is a field-based scientific expert to external and internal stakeholders focused on non-promotional information exchange, supporting data dissemination and gathering medical insights to provide patient-centric solutions. The MSL must maintain up-to-date knowledge of relevant scientific information. The MSL works as the field-based extension of Medical Affairs complying with all Ipsen SOPs, policies, directives and country guidelines Covering both Aesthetic and Therapeutic indications of Dysport.
 </li>
 <li>
 This is a field-based position, with at least 60% of the time spent engaging with external stakeholders (e.g., HCPs, KOLs, institutions) across KSA. Candidates must be comfortable with regular travel and face-to-face scientific exchange.
 
 
 </li>
 </ul>
 
 About The Role
 
 
 
 
 Establish and Foster professional collaborations with the Healthcare community :
 
 
 
 <ul>
 <li>
 Establish and maintain peer to peer relationships with key clinical and leading medical experts, professional associations and institutions in their therapeutic area
 </li>
 <li>
 Identify and update Thought Leaders (TL) information in their therapeutic area using appropriate documentation practices within the Customer Relationship Management (CRM) system and in accordance with the MSL directive and TL tiering process
 </li>
 <li>
 Conduct fair balanced, evidence based scientific exchanges with TL and others in the healthcare community to explore mutual clinical and scientific interests, discover insights, other key information and potential research collaborations
 </li>
 <li>
 Identify opportunities for collaboration with TL when aligned with Ipsen strategy
 </li>
 <li>
 Develop and enhance scientific and educational collaborations with Healthcare Professionals (HCPs) within the Healthcare community and act as a medical contact for TL and external medical experts
 </li>
 <li>
 Attend scientific/educational meetings (congresses, symposia, etc.) as required
 </li>
 <li>
 Respond to and appropriately document unsolicited requests for medical information
 </li>
 <li>
 Engage in scientific discussions and provide medical insights through field interactions (&ge;70% field time)
 </li>
 <li>
 Responsible for managing, and responding to all medical information inquiries in a timely, accurate, and compliant manner, ensuring that all scientific responses are evidence based and aligned with Ipsen Medical Information standard
 
 
 </li>
 </ul>
 
 Develop and/or implement unbiased and non-promotional scientific exchange and educational meetings &amp; activities to lead both indications Aesthetic &amp; Therapeutics
 
 
 
 <ul>
 <li>
 Provide scientific/educational presentations to HCPs:
 </li>
 <ul>
 <li>
 Reactively: on Ipsen products (on&hyphen;label and off&hyphen;label indications), on compounds in development
 </li>
 <li>
 Proactively: on disease area management (excluding single&hyphen;product presentation)
 </li>
 </ul>
 <li>
 Organise or support legitimate scientific exchange meetings
 </li>
 <li>
 Contribute to/implement medical education programs in the field
 </li>
 <li>
 Support scientific components of injector trainings, masterclasses.
 </li>
 <li>
 Partner with KOL injectors to deliver scientific content on toxin mechanism, anatomy, and treatment outcomes.
 </li>
 <li>
 Contribute to the design of scientific agendas for workshops and expert meetings.
 </li>
 <li>
 Identify gaps in injector skill levels to inform educational strategy.
 
 </li>
 </ul>
 
 Identify and share actionable medical insights and strategic information to better inform Ipsen&rsquo;s decision making
 
 
 
 <ul>
 <li>
 Collect, analyse, and report actionable insights from HCPs related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment
 </li>
 <li>
 If appropriate, organise or support Advisory Boards
 </li>
 <li>
 Attend and report significant medical information from medical congresses
 </li>
 <li>
 Engage and collaborate on specific initiatives with patient organisations in accordance with the Global Guidance on Interactions with Patient Organisations
 </li>
 <li>
 Contribute to the dissemination of the information within Ipsen as appropriate
 </li>
 <li>
 Ability to engage scientifically in both traditional and digital learning settings (webinars, hybrid educational modules).
 </li>
 <li>
 Report spontaneous potential adverse events and product&hyphen;related quality complaints in accordance to global and local SOPs
 
 
 </li>
 </ul>
 
 Support To Clinical Development &amp; ISS Data Generation
 
 
 
 <ul>
 <li>
 Coordinate and facilitate unsolicited Investigator&hyphen;Sponsored Studies (ISSs) once submitted through the ISS portal and internally approved, until completion, presentation, and publication (as approved and coordinated with Global Publications), in alignment with Medical Affairs&rsquo; objectives
 </li>
 <li>
 Support R&amp;D projects and Company Sponsored Studies (CSS) operations
 </li>
 <li>
 Support the implementation and follow&hyphen;up of post-marketing clinical activities such as registry/database projects, epidemiological surveys, post&hyphen;authorisation studies (phase IV) at the site level
 </li>
 <li>
 Identify opportunities to collect and/or analyse Real&hyphen;World&hyphen;Evidence (RWE)
 
 
 </li>
 </ul>
 
 Ensure Internal Cross-functional Collaborations As a Scientific Partner
 
 
 
 <ul>
 <li>
 Working with office-based Medical Affairs, contribute to the development of the Local Annual Medical Plan (LAMP)
 </li>
 <li>
 Develop standard response letters, if required (in coordination with Medical Information)
 </li>
 <li>
 Provide scientific expertise and training to staff as appropriate
 </li>
 <li>
 Contribute to the review and approval of promotional or non&hyphen;promotional materials from a Medical perspective in accordance with the local SOPs, if needed
 </li>
 <li>
 Attend and contribute to regional account planning/training sessions from a Medical perspective
 </li>
 <li>
 Ensure speakers briefing for promotional meetings, if needed
 </li>
 </ul>
</div>

Medical Science Liaison

IPSEN

<div><ul><li>MSL is a field-based scientific expert to external and internal stakeholders focused on non-promotional information exchange, supporting data dissemination and gathering medical insights to provide patient-centric solutions. The MSL must maintain up-to-date knowledge of relevant scientific information. The MSL works as the field-based extension of Medical Affairs complying with all Ipsen SOPs, policies, directives and country guidelines Covering both Aesthetic and Therapeutic indications of Dysport.</li><li>
This is a field-based position, with at least 60% of the time spent engaging with external stakeholders (e.g., HCPs, KOLs, institutions) across KSA. Candidates must be comfortable with regular travel and face-to-face scientific exchange.</li></ul><h2 class="jobSectionHeader">
About the Role:</h2><h3 class="jobSectionHeader">
Establish and Foster professional collaborations with the Healthcare community :</h3><ul><li>
Establish and maintain peer to peer relationships with key clinical and leading medical experts, professional associations and institutions in their therapeutic area</li><li>
Identify and update Thought Leaders (TL) information in their therapeutic area using appropriate documentation practices within the Customer Relationship Management (CRM) system and in accordance with the MSL directive and TL tiering process</li><li>
Conduct fair balanced, evidence based scientific exchanges with TL and others in the healthcare community to explore mutual clinical and scientific interests, discover insights, other key information and potential research collaborations</li><li>
Identify opportunities for collaboration with TL when aligned with Ipsen strategy</li><li>
Develop and enhance scientific and educational collaborations with Healthcare Professionals (HCPs) within the Healthcare community and act as a medical contact for TL and external medical experts</li><li>
Attend scientific/educational meetings (congresses, symposia, etc.) as required</li><li>
Respond to and appropriately document unsolicited requests for medical information</li>
Engage in scientific discussions and provide medical insights through field interactions (<li> 70% field time)</li><li>
Responsible for managing, and responding to all medical information inquiries in a timely, accurate, and compliant manner, ensuring that all scientific responses are evidence based and aligned with Ipsen Medical Information standard</li></ul><h3 class="jobSectionHeader">
Develop and/or implement unbiased and non-promotional scientific exchange and educational meetings &amp; activities to lead both indications Aesthetic &amp; Therapeutics
</h3><ul><li>Provide scientific/educational presentations to HCPs:<ul><li>
Reactively: on Ipsen products (on‐label and off‐label indications), on compounds in development</li><li>
Proactively: on disease area management (excluding single‐product presentation)</li></ul></li><li>
Organise or support legitimate scientific exchange meetings</li><li>
Contribute to/implement medical education programs in the field</li><li>
Support scientific components of injector trainings, masterclasses.</li><li>
 Partner with KOL injectors to deliver scientific content on toxin mechanism, anatomy, and treatment outcomes.</li><li>
 Contribute to the design of scientific agendas for workshops and expert meetings.</li><li>
Identify gaps in injector skill levels to inform educational strategy.</li></ul><h3 class="jobSectionHeader">
Identify and share actionable medical insights and strategic information to better inform Ipsen&rsquo;s decision making
</h3><ul><li>Collect, analyse, and report actionable insights from HCPs related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment</li><li>
If appropriate, organise or support Advisory Boards</li><li>
Attend and report significant medical information from medical congresses</li><li>
Engage and collaborate on specific initiatives with patient organisations in accordance with the Global Guidance on Interactions with Patient Organisations</li><li>
Contribute to the dissemination of the information within Ipsen as appropriate</li><li>
Ability to engage scientifically in both traditional and digital learning settings (webinars, hybrid educational modules).</li><li>
Report spontaneous potential adverse events and product‐related quality complaints in accordance to global and local SOPs</li></ul><h3 class="jobSectionHeader">
Support to clinical development &amp; ISS data generation:
</h3><ul><li>Coordinate and facilitate unsolicited Investigator‐Sponsored Studies (ISSs) once submitted through the ISS portal and internally approved, until completion, presentation, and publication (as approved and coordinated with Global Publications), in alignment with Medical Affairs&rsquo; objectives</li><li>
Support R&amp;D projects and Company Sponsored Studies (CSS) operations</li><li>
Support the implementation and follow‐up of post-marketing clinical activities such as registry/database projects, epidemiological surveys, post‐authorisation studies (phase IV) at the site level</li><li>
Identify opportunities to collect and/or analyse Real‐World‐Evidence (RWE)</li></ul><h3 class="jobSectionHeader">
Ensure internal cross-functional collaborations as a scientific partner:
</h3><ul><li>Working with office-based Medical Affairs, contribute to the development of the Local Annual Medical Plan (LAMP)</li><li>
Develop standard response letters, if required (in coordination with Medical Information)</li><li>
Provide scientific expertise and training to staff as appropriate</li><li>
Contribute to the review and approval of promotional or non‐promotional materials from a Medical perspective in accordance with the local SOPs, if needed</li><li>
Attend and contribute to regional account planning/training sessions from a Medical perspective</li><li>
Ensure speakers briefing for promotional meetings, if needed</li></ul></div>

Sundus

<div>
 
 
 Position: Material submittal Officer (Wood Factory / Joinery)
 
 
 
 
 Location: Riyadh, KSA
 
 
 
 
 Duration: Yearly Renewable
 
 
 
 
 
 
 
 
 
 Job Description:
 
 
 
 
 Description:
 
 
 
 Responsible for preparing, organizing, and following up on all Material Technical Submittals (MTS) related to wood, joinery, and finishing materials, in line with project specifications and consultant/client requirements. Ensures timely submission, tracking, approval, and compliance of all materials used in factory production and site installation.
 
 
 
 
 
 
 Roles and Responsibilities:
 
 
 <ul>
 <li>
 Review project specifications, drawings, and BOQs to identify wood, joinery, hardware, finishes, and accessories material requirements.
 </li>
 <li>
 Prepare and compile Material Technical Submittals for consultant/client approval.
 </li>
 <li>
 Coordinate with suppliers, manufacturers, and internal factory teams to collect technical data sheets, certificates, samples, and mockups.
 </li>
 <li>
 Maintain and update the Material Submittal Log (MSL) and material tracking records.
 </li>
 <li>
 Follow up on submitted materials and manage responses to consultant/client comments and revisions.
 </li>
 <li>
 Ensure all submittals comply with project standards (fire rating, sustainability, LEED if applicable, veneer/finish specifications, etc.).
 </li>
 <li>
 Coordinate with procurement to confirm approved materials prior to ordering.
 </li>
 <li>
 Liaise with factory production and site teams to ensure materials used match approved submittals.
 </li>
 </ul>
 
 
 
 
 
 Qualifications and Experience:
 
 
 <ul>
 <li>
 Diploma or Bachelor&rsquo;s degree in Engineering, Architecture, or a related field.
 </li>
 <li>
 3&ndash;4 years of experience in material submittals within wood factories, joinery, or interior fit-out projects.
 </li>
 <li>
 Strong understanding of wood materials, finishes, hardware, and joinery systems.
 </li>
 <li>
 Familiar with consultant approval processes and project documentation.
 </li>
 <li>
 Proficient in Microsoft Excel, Word, and PDF editing tools.
 </li>
 </ul>
 
 
</div>

Material Officer

<div>Market Access Head Rare Disease&ndash; KSA 
 
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.
ROLE SUMMARY<ul><li>
Leads and shapes the market access strategy for AZ Rare Disease innovative portfolio in Saudi Arabia, ensuring sustainable reimbursement, patient access, and long-term value realization.</li><li>
Provides leadership across the market access organization, ensuring strategic alignment, execution excellence, and strong people capability.</li><li>
Based in Saudi Arabia.</li><li>
Reports directly to the Market Access Director.</li></ul>
What you&rsquo;ll do
Market Access Strategy &amp; Execution<ul><li>
Set direction and priorities for Market Access strategies, objectives, and tactical plans in alignment with brand and country strategies.</li><li>
Lead the development and execution of early access strategies for existing brands and new launches, ensuring sustainable adoption within the Saudi healthcare system.</li><li>
Enable and guide teams to execute formulary listing processes and brand expansion plans through effective cross-functional collaboration.</li><li>
Drive pricing analysis and recommendations by overseeing competitive landscape assessments, customer insights, and alignment with brand value propositions.</li><li>
Shape stakeholder-informed market access strategies by anticipating stakeholder priorities, identifying partnership opportunities and business risks, and translating insights into actionable recommendations.</li><li>
Anticipate shifts in the external environment, translate insights into strategic guidance, and ensure timely organizational response.</li><li>
Work in close partnership with cross-functional teams to shape and implement market access strategies across the product lifecycle, including pre-launch readiness and launch execution.</li><li>
Partner with cross-functional teams to develop pricing and contracting strategies that optimize product positioning and enable effective pricing and contracting execution.</li><li>
Drive value-based engagement with key stakeholders to address access barriers and support informed access decision-making.</li><li>
Ensure payer-relevant evidence strategies are defined and executed, including clinical, economic, and real-world evidence.</li><li>
Guide the development of robust, localized value propositions supported by evidence, ensuring consistency and scientific rigor across teams.</li><li>
Sponsor and enable innovative projects and partnerships that address customer needs and create sustainable, win-win outcomes.</li></ul>
Stakeholder Strategy &amp; External Engagement<ul><li>
Shape and sustain strategic partnerships with Health Authorities through high-impact health initiatives aligned with national priorities.</li><li>
Set direction for stakeholder engagement strategies, ensuring alignment with the Country President and Market Access Director.</li><li>
Ensure disciplined execution and visibility of stakeholder plans by monitoring progress and communicating status to internal stakeholders.</li><li>
Foster strong, trust-based relationships with key customers and stakeholders, ensuring consistency and quality of engagement across teams.</li></ul>
Pricing Strategy &amp; Reimbursement Leadership<ul><li>
Partner with the Market Access Director and pricing teams to shape pricing and reimbursement strategies that optimize the lifetime value of AstraZeneca&rsquo;s products, in line with corporate guidance.</li><li>
Set pricing direction required to enable brand and market access strategies.</li><li>
Guide assessment of the competitive pricing landscape, ensuring insights are translated into clear, defensible pricing recommendations.</li><li>
Anticipate and assess the business impact of current and evolving market access environments and price regulation changes, supporting proactive decision-making.</li><li>
Enable the development of innovative pricing approaches, including managed entry agreements and alternative contracting models, to support sustainable access.</li><li>
Collaborate closely with the Market Access Director and Commercial leadership to define pricing strategies and optimal prices that maximize access and winning potential.</li></ul>
People Leadership &amp; Performance Management<ul><li>
Build and sustain strong Market Access capability by developing leaders and teams, strengthening critical skills, and enabling progression to advanced and leadership roles.</li><li>
Set clear performance expectations and standards, and ensure consistent performance management and coaching practices across teams.</li><li>
Identify and accelerate high-potential talent, actively building succession pipelines and supporting long-term leadership continuity.</li><li>
Lead meaningful career and development conversations, ensuring clarity on career paths, expectations, and development actions.</li><li>
Work with team members to define challenging and aligned goals across accounts, ensuring alignment with strategic priorities.</li><li>
Promote strong decision-making discipline, guiding teams to assess impact, manage risk, and make effective trade-offs that maximize business and access outcomes.</li></ul>
Collaboration &amp; Influence<ul><li>
Foster strong cross-functional collaboration across Market Access, Commercial, Medical, and Government Affairs, leveraging diverse expertise to achieve shared objectives.</li><li>
Influence outcomes without direct authority by aligning stakeholders, shaping perspectives, and motivating action through credibility, partnership, and effective communication.</li></ul>
Corporate Responsibility &amp; Compliance<ul><li>
Uphold and role-model the highest ethical standards, acting in line with AstraZeneca&rsquo;s Code of Ethics and all applicable corporate policies.</li><li>
Ensure compliance across all activities with local legislation, regulatory requirements, and corporate standards, fostering a culture of integrity and accountability.</li><li>
Ensure timely and accurate reporting, in accordance with established procedures, of health, environment, and wellbeing incidents; adverse events; and any changes in conflict of interest status.</li></ul>
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>
Bachelor&rsquo;s Degree in Pharmacy or equivalent.</li><li>
7+ years of experience with consistent success in pharmaceutical industry.</li><li>
3+ years of experience in a payer environment preferably in market access / health economic related role.</li><li>
Experience in Saudi Market is a must.</li><li>
Demonstrated strong oral, written and group communication skills.</li><li>
Interpersonal skills &ndash; Influencing, negotiation, collaboration and teamwork.</li><li>
Leadership &amp; autonomy to initiate &amp; execute responsibility under minimum guidance.</li><li>
People management experience.</li><li>
Effective analytical thinking, problem solving and decision making.</li><li>
Planning and organization skills.</li></ul>
Desirable Capabilities:<ul><li>
Post graduate university degree in health economics, epidemiology, public health, or health policy.</li><li>
Strong commercial background.</li><li>
Previous experience in different functional areas of the business.</li><li>
Previous experience in different portfolios with relevance to AstraZeneca&rsquo;s portfolio.</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>

Market Access Head RDU

<div>
 
 Site Name:
 
 Riyadh Olaya Towers
 
 
 
 Posted Date:
 
 Dec 21 2025
 
 
 
 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.
 
 
 
 
 Position Summary
 
 
 
 We are seeking a dynamic and motivated
 
 Health Technology Assessment Associate
 
 to play a pivotal role in supporting HTA activities in Saudi Arabia. Your work will contribute to ensuring patients have timely access to innovative treatments, while aligning with GSK&rsquo;s mission to get ahead of disease together.
 
 
 
 Key Responsibilities
 
 
 
 As an HTA Associate, your responsibilities will include:
 
 
 
 <ul>
 <li>
 Developing and supporting HTA submissions to local authorities, ensuring compliance with national guidelines and alignment with GSK&rsquo;s strategic objectives.
 </li>
 <li>
 Collaborating with internal teams to identify evidence gaps and develop robust evidence generation plans.
 </li>
 <li>
 Conducting health economic analyses, including cost-effectiveness and budget impact modelling, tailored to the Saudi healthcare system.
 </li>
 <li>
 Managing external vendors and consultants to ensure high-quality deliverables within agreed timelines.
 </li>
 <li>
 Monitoring the HTA and reimbursement landscape to inform GSK&rsquo;s market access strategies.
 </li>
 <li>
 Presenting findings and insights to internal and external stakeholders to support informed decision-making and enhance patient access.
 
 
 
 </li>
 </ul>
 
 Required Qualifications
 
 
 
 To succeed in this role, you should bring:
 
 
 
 <ul>
 <li>
 Saudi National.
 </li>
 <li>
 A bachelor&rsquo;s degree in pharmacy.
 </li>
 <li>
 At least 3 years of experience in health economics, market access, or HTA submissions.
 </li>
 <li>
 Strong analytical skills, with experience in health economic modelling and data interpretation.
 </li>
 <li>
 Knowledge of the Saudi healthcare system and reimbursement processes.
 </li>
 <li>
 Effective communication and collaboration skills, with the ability to work across teams and stakeholders.
 </li>
 <li>
 Proficiency in Microsoft Excel and relevant data analysis tools.
 
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 We value the following additional skills and experiences:
 
 
 
 <ul>
 <li>
 A postgraduate degree in health economics, public health, or a related field.
 </li>
 <li>
 Experience working with international stakeholders or global teams.
 </li>
 <li>
 Familiarity with real-world data sources and observational research methods.
 </li>
 <li>
 Knowledge of local and international HTA guidelines and processes.
 </li>
 <li>
 Strong project management skills, including managing timelines and budgets.
 </li>
 <li>
 Experience publishing research findings in peer-reviewed journals or presenting at conferences.
 
 
 
 </li>
 </ul>
 
 Work Environment
 
 
 
 This is an on-site role based in Riyadh, Saudi Arabia. Travel across the assigned territory may be required.
 
 
 
 How To Apply
 
 
 
 If you&rsquo;re ready to join us in this impactful role, apply today! Together, we&rsquo;ll get ahead of disease and shape the future of healthcare.
 
 
 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
 
 
 
 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>

Health Technology Assessment Associate

Explore 19+ Msl rare disease in Riyadh Saudi Arabia this January. Find roles across top companies and apply now to boost your career.

19 msl rare disease jobs IN Riyadh Saudi Arabia

MSL Rare Disease

MSL Rare Disease

Medical Science Liaison

Medical Science Liaison

Material Officer

Market Access Head RDU

Health Technology Assessment Associate