Urwah Admin

Sanofi

Sanofi est une entreprise biopharmaceutique qui innove en R&D et s'appuie sur l'IA pour améliorer la vie des gens grâce à des médicaments et vaccins innovants.

<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><h3 class="jobSectionHeader"><b><i>
About the Job:</i></b></h3><h3 class="jobSectionHeader"><b>
Our Team:</b></h3><h3 class="jobSectionHeader"><b>
The Africa medical Team at Sanofi is a high-performing team of medical leaders who are a trusted source of scientific and medical information and share insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthen our team and mirror the healthcare communities we engage.</b></h3><h3 class="jobSectionHeader"><b>
KEY RESPONSIBILITIES</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Utilize strong business acumen, acting as a key strategic business partner to the organization</b></h3></li><li><h3 class="jobSectionHeader"><b>
Initiate and drive projects to raise standards of care and change clinical practice</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ability to work independently with a solutions-oriented and balanced approach to ambiguity</b></h3></li><li><h3 class="jobSectionHeader"><b>
Lead and drive rapid integrated evidence planning and execution through deep understanding of internal and external stakeholder evidence needs and robust data gaps analysis</b></h3></li><li><h3 class="jobSectionHeader"><b>
Deep therapy area expertise and product knowledge including competitor data</b></h3></li><li><h3 class="jobSectionHeader"><b>
Drive strong collaborative relationships with commercial and cross-functional teams, including marketing, value &amp; access, health economics, regulatory and clinical</b></h3></li><li><h3 class="jobSectionHeader"><b>
Cultivate and maintain relationships with external experts</b></h3></li><li><h3 class="jobSectionHeader"><b>
Drive collaborative relationships with above-country colleagues to ensure the MCO / country involvement and strategic input into global and regional plans</b></h3></li><li><h3 class="jobSectionHeader"><b>
Good understanding of the impact and evolution of healthcare systems</b></h3></li><li><h3 class="jobSectionHeader"><b>
Lead creation and implementation of medical plans &amp; implement RMMs strategy across all countries in Africa MCO.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ability to rapidly assimilate new data and integrate into the advancement in the TA.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Create industry leading digital educational and scientific content that is timely, relevant, interactive and innovative.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Champion the patient voice when developing and implementing medical strategies</b></h3></li><li><h3 class="jobSectionHeader"><b>
Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team</b></h3></li><li><h3 class="jobSectionHeader"><b>
Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team</b></h3></li></ul><p></p><h3 class="jobSectionHeader"><b><i>
About You:
</i></b></h3><h3 class="jobSectionHeader"><b>Education</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Bachelor&rsquo;s degree in pharmacy, Medicine. Medical Degree or equivalent medical degree preferred, PhD or PharmD</b></h3></li></ul><h3 class="jobSectionHeader"><b>
Professional Experience</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Good understanding of the continuum of data generation including clinical development, Real World Evidence (RWE) and data gaps analysis</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ability to act independently with a solutions-oriented and balanced approach to the grey areas</b></h3></li><li><h3 class="jobSectionHeader"><b>
Excellent communication skills including driving challenging discussions&middot; Develop a good understanding of HCP communication preferences to adapt communication style and optimize use of relevant channels to suit</b></h3></li><li><h3 class="jobSectionHeader"><b>
Implement true scientific engagement journeys by bridging channel disconnect to drive ongoing engagement and grow collaborative opportunities and meaningful scientific exchange</b></h3></li><li><h3 class="jobSectionHeader"><b>
Be confident in the use of Omnichannel tools and ability to adapt to new channels</b></h3></li><li><h3 class="jobSectionHeader"><b>
Effectively and compliantly share unmet needs of HCPs and their centers with cross-functional teams to inform patient centric strategy</b></h3></li></ul><h3 class="jobSectionHeader"><b>
Take the Lead Values
</b></h3><ul><li><h3 class="jobSectionHeader"><b>Aim Higher:</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>
Act for Patients:</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>
Be Bold:</b><b> Take thoughtful risks, seize opportunities and think beyond what's possible to accelerate our science and drive compelling growth.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Lead Together:</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 where patient insights shape drug development.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Lead a high-impact portfolio with bold ambitions and significant upcoming launches.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Explore bold career paths &ndash; with opportunities to grow through scientific, leadership, and cross-functional</b></h3></li></ul></div>

Egypt Oncology Medical Manager

<div><p><b>Job title</b>: Commercial Lead &ndash; Autoimmune Type 1 Diabetes, Greater Gulf</p><ul><li><p>
Riyadh, Kingdom of Saudi Arabia</p></li></ul><p></p><p><b>
About the job</b></p><p>
As Commercial Lead &ndash; Autoimmune Type 1 Diabetes within our General Medicines team, you'll drive commercial strategy and market growth for an innovative and high-priority portfolio across Saudi Arabia and the broader Gulf region. Ready to get started?</p><p>
Join the team transforming how healthcare is delivered for chronic and specialty conditions worldwide. In General Medicines, you'll help drive meaningful outcomes in diabetes, transplant, and immunology &ndash; with the scale and urgency patients deserve. Based in Riyadh, you'll play a pivotal role in shaping the future of autoimmune Type 1 diabetes care across the Greater Gulf, leading cross-functional initiatives and building the partnerships that make a real difference for patients.</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>Develop and implement commercial strategies for the AT1D portfolio aligned with regional and global priorities; manage full P&amp;L responsibility including annual budgets, forecasts, and resource allocation to maximize return on investment.</li><li>Define and track performance metrics, identify market opportunities, and translate insights from the competitive landscape and emerging therapies into actionable plans that accelerate growth and increase market share.</li><li>Partner with market access teams to build compelling value propositions and health economic narratives, securing optimal pricing and reimbursement outcomes across Gulf markets.</li><li>Build and maintain strategic relationships with key opinion leaders, healthcare professionals, payers, and patient organizations; represent Sanofi at external meetings, conferences, and industry events.</li><li>Lead cross-functional collaboration across Medical Affairs, Regulatory, Market Access, and Marketing to deliver integrated brand strategies and co-lead product launch preparations that differentiate our offerings in the market.</li><li>Provide strategic direction and coaching to the sales organization, developing innovative customer engagement models and championing agile ways of working across the commercial team.</li><li>Ensure all commercial activities are conducted in full compliance with local regulations, industry codes, and company policies, fostering a culture of integrity throughout the organization.</li></ul><p></p><p><b>
About you</b></p><ul><li><b>Experience:</b> Significant experience in progressive commercial leadership roles within the pharmaceutical or healthcare industry, with a strong track record in specialty care markets; background in diabetes is a plus. Demonstrated experience managing P&amp;L, leading cross-functional teams, and operating effectively in matrix organizations.</li><li><b>Soft and technical skills:</b> Strong strategic thinking and business acumen; excellent communication, negotiation, and interpersonal skills; results-oriented with an entrepreneurial and patient-centric mindset; proven ability to engage and influence senior stakeholders across diverse functions and cultures.</li><li><b>Education:</b> Bachelor's degree required; advanced degree in Business, Healthcare, or a related field preferred.</li><li><b>Languages:</b> Fluent in both English and Arabic.</li><li>Proven people management experience, with the ability to inspire, coach, and develop teams.</li><li>In-depth knowledge of Greater Gulf healthcare systems, market dynamics, and regulatory and market access environments.</li><li>Willingness and ability to travel up to 60% across the Greater Gulf region and periodically to regional and global meetings.</li></ul><p></p><p><b>
Why choose us?</b></p><ul><li>Help shape the future of care for chronic and complex conditions like aT1D, Type 2 diabetes, transplant, and cardiovascular disease.</li><li>Drive meaningful impact at global scale: our medicines reach more than 100 million people each year.</li><li>Turn bold ideas into breakthrough launches, with multiple new therapies planned through 2030 and beyond.</li><li>Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.</li><li>Take the lead on one of the most exciting and fast-evolving areas in diabetes care &ndash; autoimmune Type 1 diabetes &ndash; at a pivotal moment in the treatment landscape across the Gulf.</li><li>Build your influence at the heart of a high-growth region, working at the intersection of commercial strategy, market access, and patient advocacy in a dynamic and diverse healthcare environment.</li><li>Be part of a team where entrepreneurial thinking is encouraged and your decisions have a direct, visible impact on patients and business outcomes across Saudi Arabia and neighboring Gulf markets.</li></ul><p><b>
Pursue </b><b><i>Progress</i></b><b>. Discover </b><b><i>Extraordinary</i></b><b>.</b></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>
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Commercial Lead AT1D

<div><p><b>Job title</b><b>:</b><b> </b>Clinical Research Director (CRD)</p><p><b>
Location: </b>Cambridge, MA / Morristown, NJ</p><p></p><p><b><br>
About the job</b></p><p>
Join the engine of Sanofi&rsquo;s mission &mdash; where deep immunoscience meets bold, AI-powered research. In R&amp;D, you&rsquo;ll drive breakthroughs that could turn the impossible into possible for millions.</p><p></p><p><b>
Our Team:</b></p><p>
To support sustainable growth Sanofi Global Development ambition is to be the industry-leading Development organization, using impactful therapeutic innovation that turns hope into reality for people.Therapeutic Areas lead the development of therapies by overseeing the portfolio of development projects and execution of the development programs through the multi-disciplinary Global Project Team (GPT).</p><p></p><p><br>
The <b>Clinical Research Directo</b><b>r</b><b> (CRD) </b>is the <b>medical expert in the Development of R&amp;D programs</b>. The role requires a well-organized, strategically and, operationally focused, resourceful individual with very good emotional intelligence, self-motivation, solid analytical skills, and the ability deliver to multiple tasks.</p><p></p><p><b><br>
Our Project:</b></p><p>
Lunsekimig is a novel bi-specific nanobody targeting both TSLP and IL-13. Lunsekimig is in development across multiple immunology disease areas. We are seeking a highly motivated clinician-scientist to lead clinical trials in the respiratory space.</p><p></p><p><b>
About Sanofi</b></p><p>
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.</p><p></p><p><b>
Main responsibilities:</b></p><p>
The role of the CRD is to:</p><ul><li><p>
Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs</p></li><li><p>
Collaborate with other medical and clinical scientific experts DMDs or DSDs in the project under the leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy and prepare/assist with regulatory bodies interaction</p></li><li><p>
Develop the study level regulatory documentation (Abbreviated Protocol, Protocol, Amended protocol) for their project, lead other development activities pertaining to study start-up (e.g. pressure test, competitive intelligence, patient engagement, cluster feasibility, study risk assessment etc&hellip;)</p></li><li><p>
Provide appropriate medical input &amp; support for all activities related to clinical studies conduct such as answers to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the Centralized monitoring, clinical and medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators</p></li><li><p>
Contribute to the clinical part of Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc&hellip;) and answer to questions from health authorities.</p></li><li><p>
Be the medical reference in the Clinical Study team, ensuring the medical relevance of the clinical data</p></li></ul><p></p><p><b>
Key responsibilities include:</b></p><p><b>
Leading the clinical development plan strategies</b></p><ul><li><p>
Responsible for the clinical development plans and clinical sections of integrated development plans (IDP)</p></li><li><p>
Collaborate with other CRDs/DSDs within the project, ensures leadership, builds consensus, coordinates action plans with stakeholders to resolve project-related issues, anticipates potential issues (sharing lessons learned) across the project or study teams</p></li><li><p>
Raise study or project-level issues to the project head and propose related corrective action plans</p></li><li><p>
Contribute in the definition of the product value proposition (TVP), Target Product Profile (TPP) and market access strategy (in collaboration with respective functions) and the focus of the research strategy, by providing input on existing clinical needs and approaches to clinical development strategies for research projects</p></li><li><p>
Collaborates with external partners, regulators, scientific experts and internal stakeholders
</p></li><li><p>Provide operational expertise to project clinical sub team, as needed</p></li><li><p>
Evaluates relevant medical literature and status from competitive products</p></li></ul><p><b>
Lead, Support and oversee the execution of clinical development and studies
</b></p><ul><li><p>Collaborate and communicate appropriately with all function stakeholders (e.g. clinical operations, project management, Patient Safety and Pharmacovigilance, regulatory, Finance, Scientific External Engagement, Procurement etc&hellip;), responsible for timelines, budgets and contingency/risk management plans to assure successful execution of the clinical trials in compliance with Good Clinical Practice (GCP), applicable laws and regulations as well as applicable standard operating procedures (SOPs)
</p></li><li><p>Develop the abbreviated protocol, the final protocol and protocol amendments
</p></li><li><p>Develop/review the Core Study Informed Consent Form (CSICF)</p></li><li><p>
Develop/review Study committee Charters</p></li><li><p>
Collaborate on key medical and clinical questions with the Global feasibility manager to prepare and interpret feasibility and competitive intelligence results
</p></li><li><p>Review and provide clinical input across different study documents Vendors RFPs, e-CRF, eCOA etc</p></li><li><p>
Provide medical/clinical input to study-related documents such as study plans e.g. Study risk management plan, Monitoring and centralized monitoring plans
</p></li><li><p>Participate in the elaboration of training material and presentations at the investigator meetings/local teams trainings</p></li><li><p>
Answer to medical questions raised by HA, EC/IRBs, sites</p></li><li><p>
Ensure quality of clinical data through continuous data validation, blinded Data review on summary tables or electronic data visualization during clinical trial conduct (AE dedicated review, and Clinical Case review for safety data and statistical surveillance for efficacy data,&hellip;)
</p></li><li><p>Ensure trial master file documents readiness and availability, and mandatory trainings linked to the clinical function</p></li><li><p>
Lead the study specific committees (IDMC, steering com, adjudication &hellip;) with operational support
</p></li><li><p>Co-Develop the SAP in collaboration with biostatistical team</p></li><li><p>
Responsible for key results preparation</p></li><li><p>
Develop/Review the clinical study report
</p></li></ul><p><b>Responsibilities related to regulatory and safety documents and meetings</b></p><ul><li><p>
Review and/or contribute in the clinical section of the Investigator&rsquo;s brochure, CTA, IND, DSUR, DRMP, RMP</p></li><li><p>
Write/review the clinical sections of the BLA/CTD, Briefing packages for regulatory meetings, PSP/PIP</p></li><li><p>
Ensures clinical data meets all necessary regulatory standards</p></li><li><p>
Collaborates with the Patient Safety GSO to detect and document any safety signal</p></li><li><p>
Participates in Advisory Committee preparation</p></li></ul><p><b>
Scientific Data evaluation and authorship</b></p><ul><li><p>
Participate and author manuscripts and abstracts
</p></li><li><p>Establish and maintains appropriate collaborations with knowledge experts or advisory boards</p></li><li><p>
Contribute on an ad hoc basis to specific tasks such as the evaluation of potential in-licensing candidates for the therapeutic area and serves as the clinical advisor to research teams</p></li></ul><p></p><p><b><br>
About you</b></p><p><b>
Experience</b><b>:</b></p><ul><li><p>
At least 3 years previous experience in clinical development in pharmaceutical industry or a CRO or medical experience in clinical development in an Healthcare institution. Background in respiratory, allergy, or immunology preferred.</p></li></ul><p><b>
Soft skills</b><b>:</b></p><ul><li><p>
Very good communication skills (verbal and written) for interactions across functional areas and for interactions with key regulatory agencies</p></li><li><p>
Excellent problem solving capability</p></li><li><p>
Demonstrated capability to challenge decision and status quo with a risk-management approach</p></li><li><p>
Ability to negotiate to ensure operational resources are available for continued clinical conduct</p></li><li><p>
Very good teaching skills, demonstrated ability to assist and train others</p></li><li><p>
Ability to work within a matrix model</p></li><li><p>
International/ intercultural working skills</p></li><li><p>
Open-minded to apply new digital solutions</p></li></ul><p><b>
Technical skills</b><b>:</b></p><ul><li><p>
Understanding of pharmaceutical product development and life cycle management</p></li><li><p>
Very good Scientific and medical/clinical expertise</p></li><li><p>
Very good expertise in clinical development and methodology of clinical studies</p></li></ul><p><b>
Education:</b></p><ul><li><p>
MD (Doctor of Medicine) or equivalent patient care-related medical degree (DO, international equivalents, etc.) required</p></li></ul><p><b>
Languages</b>:</p><ul><li><p>
English fluent (spoken and written)</p></li></ul><p></p><p><b>
Why Choose Us?</b></p><ul><li><p>
Bring the miracles of science to life alongside a supportive, future-focused team.</p></li><li><p>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</p></li><li><p>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</p></li><li><p>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks&rsquo; gender-neutral parental leave.</p></li></ul><p></p><p>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.</p><p>
#GD-SA
<br>
#LI-SA</p><p>
#LI-Onsite</p><p>
#vhd</p><p>
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.</p></div>

Clinical Research Director, I&I

<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>
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Partner Market PV Manager – Sub Saharan Africa

Partner Market PV Manager – Sub Saharan Africa