Urwah Admin

Sanofi

<div><div><div><div><p><b>Job title: </b>Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI)</p><ul><li><b>
Location:</b> <i>Riyadh, Kingdom of Saudi Arabia</i></li></ul><p></p><p><b>
About the job</b></p><p>
As a <b>Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI)</b> within our Specialty Care team, you'll serve as the vital bridge between cutting-edge science and clinical practice. You'll build trusted relationships with key scientific experts, support clinical research initiatives, and bring real-world medical insights back to our brand teams to help shape breakthrough treatments for patients with immune challenges. Ready to get started?</p><p>
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.</p><p></p><p><b>
About Sanofi</b></p><p>
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.</p><p></p><p><b>
Main responsibilities</b></p><ul><li>
Build and maintain balanced scientific relationships with key external experts to deepen understanding of customer research needs and opportunities in Immunology (Respiratory &amp; GI).</li><li>
Develop a clear understanding of the healthcare ecosystem through stakeholder mapping and identifying key milestones in patient journeys.</li><li>
Provide healthcare professionals and decision-makers with accurate, balanced, and timely scientific information about our Immunology portfolio.</li><li>
Collaborate closely with Medical Affairs and clinical teams to coordinate Phase IV clinical projects, facilitate investigator-sponsored study submissions, support publications, and assist in site selection.</li><li>
Act as a product expert supporting commercial teams during training sessions, particularly in handling medical objections.</li><li>
Serve as the primary source of real-world medical insights and scientific expert feedback from the field to brand teams.</li><li>
Represent Sanofi at key medical and scientific conferences by staffing medical information booths, gathering competitive intelligence, and observing sponsored speakers.</li><li>
Receive, document, and report adverse events according to company procedures and ensure risk management plan implementation and monitoring.</li></ul><p><b>
About you</b></p><ul><li><b>
Education:</b> University degree in life sciences required; MD, PhD, or PharmD strongly preferred</li><li><b>
Experience:</b> At least 2 years of experience in specialty care and/or Immunology/Gastroenterology is a plus</li><li><b>
Technical skills:</b> Strong knowledge of clinical research methodology and Good Clinical Practice (GCP)</li><li><b>
Communication skills:</b> Ability to communicate effectively at various management levels, including with scientific external experts</li><li><b>
Soft skills:</b> Self-motivated team player with business acumen, resource planning abilities, and the capacity to inspire and motivate others</li><li><b>
Languages:</b> Full professional proficiency in English and Arabic</li></ul><p><b>
Why choose us?</b></p><ul><li>
Work at the intersection of cutting-edge immunoscience and patient care, helping deliver breakthrough treatments to those with the highest unmet medical needs.</li><li>
Build meaningful relationships with leading scientific experts and key opinion leaders while contributing to clinical research that shapes the future of Immunology care.</li><li>
Develop your career in a purpose-driven environment with opportunities to grow across therapeutic areas, functions, and geographies.</li><li>
Collaborate with diverse, multidisciplinary teams across Medical Affairs, Clinical Research, and Commercial functions to drive patient impact.</li><li>
Thrive in a workplace that values scientific excellence, ethical leadership, and your personal well-being with comprehensive benefits and flexible working options.</li></ul><p><b>
Pursue</b> <i>Progress</i>. <b>Discover</b> <i>Extraordinary.</i></p><p>
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue <i>Progress</i> and Discover <i>Extraordinary</i> &ndash; together.</p><p>
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law</p></div></div></div>
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Medical Science Liaison

<div><p><b>Work Schedule: </b>Mon-Fri; 9am-5pm ET (20-40 hours per week)</p><p><b>
Location: </b>100% Remote</p><div><b>
Contract Length:</b> 12-months<br>
<br>
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Part Time Medical Writer II for a 12-month contract.<br>
<br>
Job Summary:<br>
We are seeking a detail-oriented and innovative professional to join our team in creating accurate, engaging, and compliant digital content for diverse promotional channels within the healthcare sector. This position focuses on developing high-quality marketing materials that resonate with target audiences while maintaining strict adherence to regulatory standards. The successful candidate will collaborate closely with marketing teams and leverage cutting-edge AI-driven tools to streamline content development processes. This role offers the opportunity to work at the intersection of healthcare communications, digital marketing, and emerging technologies, making a meaningful impact on how healthcare information reaches and engages audiences across multiple platforms.<br>
<br>
Responsibilities:<br>
<ul><li>Collaborate with marketing teams to develop and refine digital copy for websites, email campaigns, social media, and other promotional channels</li><li>Adapt content from existing commercial and medical assets, ensuring clarity and alignment with brand messaging</li><li>Utilize large language models and AI tools to generate initial drafts and enhance efficiency in content creation</li><li>Review and fine-tune AI-generated content to correct inaccuracies, improve tone, and ensure compliance with regulatory standards</li><li>Verify references and source materials to maintain accuracy, credibility, and adherence to healthcare regulations</li><li>Navigate the Medical, Legal, Regulatory compliance and review process effectively</li><li>Stay informed on industry trends, compliance requirements, and emerging AI technologies to optimize content strategies</li><li>Manage multiple projects simultaneously and meet deadlines in a fast-paced environment</li></ul><br>
Skills:<br>
<ul><li>Strong understanding of healthcare terminology, compliance standards, and promotional guidelines</li><li>Excellent writing, editing, and proofreading skills with exceptional attention to detail and accuracy</li><li>Familiarity with AI tools and content generation platforms</li><li>Knowledge of digital marketing strategies and SEO best practices</li><li>Understanding of FDA, EMA, or other regulatory guidelines for healthcare communications</li><li>Proficiency in content management systems and marketing automation tools</li><li>Strong collaborative and communication abilities</li></ul><br>
Experience:<br>
<ul><li>5+ years of experience in healthcare marketing, medical writing, or related roles</li></ul><br>
Qualifications:<br>
<ul><li>Bachelor's degree in Marketing, Communications, Journalism, or a related field</li></ul><br>
This is an exciting opportunity to work with a leading organization in the pharmaceutical industry while enjoying the flexibility of a fully remote position. You will be at the forefront of integrating innovative AI technologies into healthcare communications, helping to shape the future of digital marketing in this critical sector. The role offers the perfect balance of creative content development and technical innovation, allowing you to expand your expertise while contributing to meaningful healthcare initiatives that impact patients and healthcare professionals worldwide.</div></div>

Part - Time Medical Writer II (Clinical) (contract)

<div>
 <strong>
  About Sanofi
  <br/>
  <br/>
 </strong>
 We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people&rsquo;s lives.
 <br/>
 <br/>
 <strong>
  About The Job
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Define, implement and maintain the Partner Market PV business model under the direction of the Multi-Country Safety Head ((M)-CSH). ensure an effective oversight and management of the Partner Market Service Providers (PMSP) across the MCO/region including regular meetings with the PMSPs, monitoring compliance with the PV Agreements (PVAs) and maintenance of the PVA.
  </li>
  <li>
   Ensure the implementation of PV in assigned territories, acting as the interface between PSPV, the (M)CSH and the PMSPs.
  </li>
  <li>
   Transversal coordination: ensures PV training, processes and tools are in place with the PMSPs, ensures that they are compliant with PV standards and are harmonized across countries. The Partner Market PV Manager shall identify areas of risk and escalate and work with stakeholders to resolve. Promote and deploy initiatives aimed at harmonizing and promoting best practices across PMSPs within assigned territory (if applicable). In addition, when appropriate, he/she may need to work collaboratively with the Global PSPV SMEs in developing process-related solutions oriented at the PMSPs as well as interacting closely with other PSPV functions to contribute to the appropriate management of the Sanofi PV system.
  </li>
  <li>
   Is the contact point between PMSPs and the Global PV teams, and performs other activities which require a coordination role as new process implementation, communication to partners, implementation of additional Risk Minimization Measures and its tracking, contribution to the PSMF, supports Inspection and Audit activities etc.
  </li>
  <li>
   Work collaboratively with other Sanofi functions contributing to the success of the PMSPs collaboration.
  </li>
  <li>
   Serves as back-up for Partner Market PV Managers in other territories/Regions as required
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Accountabilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Manage great customer experience: Acts as the contact point/interface between PSPV/internal and external stakeholders (i.e Partner Market Service Providers)
  </li>
  <li>
   Oversees the Partner Market Service Providers ensuring the maintenance and compliance with the PVAs. Ensures all Partner Market Service Providers meet KPIs set by PSPV, and oversee compliance of partners with applicable regulations.
  </li>
  <li>
   Routine management and support of the PV aspects of the Partner Market Services Providers, including support for audit and inspection.
  </li>
  <li>
   Participates in the Due diligence activities to select the service provider for PV activities when applicable.
  </li>
  <li>
   Follows up overall project implementation plan for new Partner Markets implementation, which involves the transition of PV activities to partners in countries in scope and ensure no noncompliance.
  </li>
  <li>
   Keeps the Multi-Country Safety Head informed on the status of the allocated Partnerships escalating issues as needed.
  </li>
  <li>
   Ensures the Multi-Country Safety Head has the comprehensive oversight and management of all the partnerships for the delegated PV activities including monitoring and enforcement of Partners compliance with the PV Agreements.
  </li>
  <li>
   In collaboration with other Partner Market PV Managers: Coordinates the implementation of the PV activities consistently across PMSPs in the assigned territories when applicable. Ensures back-up functions are in place across MCO/Regions as applicable.
  </li>
  <li>
   Is in charge of the monitoring of the budget of PMSP activities, in collaboration with the (M)-CSH.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education
  <br/>
  <br/>
 </strong>
 <em>
  About you
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   MD, Pharmacist, PhD or master&rsquo;s degree in Human Health Sciences
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience &amp; Knowledge
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum 4 years&rsquo; experience in managing Pharmacovigilance activities in close collaboration with key departments (Medical Affairs, Regulatory, Clinical, Quality Assurance, etc.) or equivalent experience.
  </li>
  <li>
   Experience working in multinational environment, across diverse cultures
  </li>
  <li>
   Experience with PV agreements and or PV partnerships and partner/vendor relations
  </li>
  <li>
   Experience in transversal projects
  </li>
  <li>
   Knowledge of other languages, Fluency in French is advantageous.
  </li>
  <li>
   Country PV experience is an asset.
  </li>
  <li>
   Experience with Clinical Safety related activities can be a plus
  </li>
  <li>
   Knowledge of other languages. Fluency in French is advantageous
  </li>
  <li>
   Project management experience.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Excellent organizational and planning capabilities
  </li>
  <li>
   Strong negotiation skills
  </li>
  <li>
   Strong interpersonal skills
  </li>
  <li>
   Strong leadership competencies
  </li>
  <li>
   Team player
  </li>
  <li>
   Fluency in English (both oral and written, including technical terminology) and communication skills (oral/written)
  </li>
  <li>
   Inter-cultural skills/ability to work across cultures.
  </li>
  <li>
   Demonstrate problem solving skills, sense of urgency, especially with respect to enforcing safety rules and global procedures as described in QDs, Operational Manuals and Guidance documents. Capacity to work under pressure
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Take The Lead Values
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Aim Higher - Focus on what matters, set high standards and move with urgency, learning from setbacks as we go to achieve higher performance.
  </li>
  <li>
   Act for patients - Never compromise on integrity, eliminate barriers, and partner with others to go faster and further for patients.
  </li>
  <li>
   Be Bold - Take thoughtful risks, seize opportunities and think beyond what&rsquo;s possible to accelerate our science and drive compelling growth.
  </li>
  <li>
   Lead Together - Build trust and collaborate openly on our shared goals, celebrate collective wins and foster a sense of belonging.
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  Why choose us?
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
  </li>
  <li>
   Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
  </li>
  <li>
   Help improve the lives of millions of people globally by making drug development quicker and more effective.
  </li>
  <li>
   Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
  </li>
  <li>
   Accelerate your professional development with structured career paths designed for both scientific and leadership advancement. Grow in ways you never imagined through bold moves that stretch your potential, cross moves into other business areas, and short-term gigs that build your scientific expertise.
  </li>
  <li>
   Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
  </li>
  <li>
   Achieve genuine work-life balance in a supportive R&amp;D environment.
  </li>
  <li>
   Enjoy outstanding benefits, including flexible working options, comprehensive healthcare, and well-being programs designed to help you thrive.
   <br/>
   <br/>
  </li>
 </ul>
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</div>


Partner Market PV Manager – Sub Saharan Africa

<div><h3 class="jobSectionHeader"><b><i>About Sanofi:</i></b></h3><h3 class="jobSectionHeader"><b>
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people&rsquo;s lives.</b></h3><p></p><h3 class="jobSectionHeader"><b><i>
About the job</i></b></h3><ul><li><h3 class="jobSectionHeader"><b>
Define, implement and maintain the Partner Market PV business model under the direction of the Multi-Country Safety Head ((M)-CSH). ensure an effective oversight and management of the Partner Market Service Providers (PMSP) across the MCO/region including regular meetings with the PMSPs, monitoring compliance with the PV Agreements (PVAs) and maintenance of the PVA.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ensure the implementation of PV in assigned territories, acting as the interface between PSPV, the (M)CSH and the PMSPs.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Transversal coordination: ensures PV training, processes and tools are in place with the PMSPs, ensures that they are compliant with PV standards and are harmonized across countries. The Partner Market PV Manager shall identify areas of risk and escalate and work with stakeholders to resolve. Promote and deploy initiatives aimed at harmonizing and promoting best practices across PMSPs within assigned territory (if applicable). In addition, when appropriate, he/she may need to work collaboratively with the Global PSPV SMEs in developing process-related solutions oriented at the PMSPs as well as interacting closely with other PSPV functions to contribute to the appropriate management of the Sanofi PV system.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Is the contact point between PMSPs and the Global PV teams, and performs other activities which require a coordination role as new process implementation, communication to partners, implementation of additional Risk Minimization Measures and its tracking, contribution to the PSMF, supports Inspection and Audit activities etc.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Work collaboratively with other Sanofi functions contributing to the success of the PMSPs collaboration.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Serves as back-up for Partner Market PV Managers in other territories/Regions as required</b></h3></li></ul><p></p><h3 class="jobSectionHeader"><b>
Key Accountabilities:</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Manage great customer experience: Acts as the contact point/interface between PSPV/internal and external stakeholders (i.e Partner Market Service Providers)</b></h3></li><li><h3 class="jobSectionHeader"><b>
Oversees the Partner Market Service Providers ensuring the maintenance and compliance with the PVAs. Ensures all Partner Market Service Providers meet KPIs set by PSPV, and oversee compliance of partners with applicable regulations.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Routine management and support of the PV aspects of the Partner Market Services Providers, including support for audit and inspection.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Participates in the Due diligence activities to select the service provider for PV activities when applicable.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Follows up overall project implementation plan for new Partner Markets implementation, which involves the transition of PV activities to partners in countries in scope and ensure no noncompliance.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Keeps the Multi-Country Safety Head informed on the status of the allocated Partnerships escalating issues as needed.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ensures the Multi-Country Safety Head has the comprehensive oversight and management of all the partnerships for the delegated PV activities including monitoring and enforcement of Partners compliance with the PV Agreements.</b></h3></li><li><h3 class="jobSectionHeader"><b>
In collaboration with other Partner Market PV Managers: Coordinates the implementation of the PV activities consistently across PMSPs in the assigned territories when applicable. Ensures back-up functions are in place across MCO/Regions as applicable.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Is in charge of the monitoring of the budget of PMSP activities, in collaboration with the (M)-CSH.</b></h3></li></ul><h3 class="jobSectionHeader"><b><i>
About you
</i></b></h3><h3 class="jobSectionHeader"><b>Education:</b></h3><ul><li><h3 class="jobSectionHeader"><b>
MD, Pharmacist, PhD or master&rsquo;s degree in Human Health Sciences</b></h3></li></ul><h3 class="jobSectionHeader"><b>
Experience &amp; knowledge:</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Minimum 4 years&rsquo; experience in managing Pharmacovigilance activities in close collaboration with key departments (Medical Affairs, Regulatory, Clinical, Quality Assurance, etc.) or equivalent experience.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Experience working in multinational environment, across diverse cultures</b></h3></li><li><h3 class="jobSectionHeader"><b>
Experience with PV agreements and or PV partnerships and partner/vendor relations</b></h3></li><li><h3 class="jobSectionHeader"><b>
Experience in transversal projects</b></h3></li><li><h3 class="jobSectionHeader"><b>
Knowledge of other languages, Fluency in French is advantageous.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Country PV experience is an asset.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Experience with Clinical Safety related activities can be a plus</b></h3></li><li><h3 class="jobSectionHeader"><b>
Knowledge of other languages. Fluency in French is advantageous</b></h3></li><li><h3 class="jobSectionHeader"><b>
Project management experience.</b></h3></li></ul><h3 class="jobSectionHeader"><b>
Competencies:</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Excellent organizational and planning capabilities</b></h3></li><li><h3 class="jobSectionHeader"><b>
Strong negotiation skills</b></h3></li><li><h3 class="jobSectionHeader"><b>
Strong interpersonal skills</b></h3></li><li><h3 class="jobSectionHeader"><b>
Strong leadership competencies</b></h3></li><li><h3 class="jobSectionHeader"><b>
Team player</b></h3></li><li><h3 class="jobSectionHeader"><b>
Fluency in English (both oral and written, including technical terminology) and communication skills (oral/written)</b></h3></li><li><h3 class="jobSectionHeader"><b>
Inter-cultural skills/ability to work across cultures.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Demonstrate problem solving skills, sense of urgency, especially with respect to enforcing safety rules and global procedures as described in QDs, Operational Manuals and Guidance documents. Capacity to work under pressure</b></h3></li></ul><p></p><h3 class="jobSectionHeader"><b><i>
Take The Lead Values:</i></b></h3><ul><li><h3 class="jobSectionHeader"><b><i>
Aim Higher</i></b><b> - Focus on what matters, set high standards and move with urgency, learning from setbacks as we go to achieve higher performance.</b></h3></li><li><h3 class="jobSectionHeader"><b>
 </b><b><i>Act for patients</i></b><b> - Never compromise on integrity, eliminate barriers, and partner with others to go faster and further for patients.</b></h3></li><li><h3 class="jobSectionHeader"><b>
 </b><b><i>Be Bold</i></b><b> - Take thoughtful risks, seize opportunities and think beyond what&rsquo;s possible to accelerate our science and drive compelling growth.</b></h3></li><li><h3 class="jobSectionHeader"><b><i>
Lead Together</i></b><b> - Build trust and collaborate openly on our shared goals, celebrate collective wins and foster a sense of belonging.</b></h3></li></ul><h3 class="jobSectionHeader"><b><i>
Why choose us?</i></b></h3><ul><li><h3 class="jobSectionHeader"><b>
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Help improve the lives of millions of people globally by making drug development quicker and more effective.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Accelerate your professional development with structured career paths designed for both scientific and leadership advancement. Grow in ways you never imagined through bold moves that stretch your potential, cross moves into other business areas, and short-term gigs that build your scientific expertise.
</b></h3></li><li><h3 class="jobSectionHeader"><b>Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Achieve genuine work-life balance in a supportive R&amp;D environment.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Enjoy outstanding benefits, including flexible working options, comprehensive healthcare, and well-being programs designed to help you thrive.</b></h3></li></ul>
null</div>

Join Sanofi and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Sanofi

About Company

Medical Science Liaison

Part - Time Medical Writer II (Clinical) (contract)

Partner Market PV Manager – Sub Saharan Africa

Partner Market PV Manager – Sub Saharan Africa