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associate medical safety director sponsor dedicated

IQVIA

<div><div><div>New Cairo, Egypt | Full time | Home-based | R1533906</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><br>
Our ever-growing <b>Lifecycle Safety Medical</b> team is expanding. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios, conducting medical evaluation of post-marketing adverse drug reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations.</div><div>
Associate Medical Safety Director</div><div>
Role responsibilities:</div><ul><li><div>
Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product&rsquo;s safety profile</div></li><li><div>
Leads signal detection and analysis, including, signal detection strategy, frequency, and timing, reviews the Signal Detection Reports and other sources of data as applicable, raises potential signals for team discussion, contributes to safety analysis reports presentations of signal evaluation data as appropriate</div></li><li><div>
Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports</div></li><li><div>
Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies</div></li><li><div>
Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up</div></li><li><div>
Providing safety oversight and contribution for label development, review, and updates</div></li><li><div>
Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document</div></li><li><div>
Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary and serve as an internal consultant to pharmacovigilance case processing teams</div></li><li><div>
Representing safety and clinical data review findings during internal and external stakeholder meetings</div></li><li><div>
Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed</div></li></ul><div>
Do you have the skills, experience and qualification required for the role:</div><ul><li><div>
A medical degree from an accredited and internationally recognized medical school</div></li><li><div>
Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience</div></li><li><div>
Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process</div></li><li><div>
Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature</div></li><li><div>
Experience in Signal detection, Aggregate reports and Risk management.</div></li><li><div>
Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing</div></li><li><div>
Ability to establish and meet priorities, deadlines, and objectives</div></li><li><div>
Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs</div></li><li><div>
Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed</div></li></ul><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div></div></div><div></div>

Associate Medical Safety Director- Sponsor Dedicated

<div>
 Our ever-growing
 <strong>
  Lifecycle Safety Medical
 </strong>
 team is expanding. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios, conducting medical evaluation of post-marketing adverse drug reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations.
 <br/>
 <br/>
 Associate Medical Safety Director
 <br/>
 <br/>
 <strong>
  Role Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product&rsquo;s safety profile
  </li>
  <li>
   Leads signal detection and analysis, including, signal detection strategy, frequency, and timing, reviews the Signal Detection Reports and other sources of data as applicable, raises potential signals for team discussion, contributes to safety analysis reports presentations of signal evaluation data as appropriate
  </li>
  <li>
   Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
  </li>
  <li>
   Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
  </li>
  <li>
   Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up
  </li>
  <li>
   Providing safety oversight and contribution for label development, review, and updates
  </li>
  <li>
   Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
  </li>
  <li>
   Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary and serve as an internal consultant to pharmacovigilance case processing teams
  </li>
  <li>
   Representing safety and clinical data review findings during internal and external stakeholder meetings
  </li>
  <li>
   Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed
   <br/>
   <br/>
  </li>
 </ul>
 Do you have the skills, experience and qualification required for the role:
 <br/>
 <br/>
 <ul>
  <li>
   A medical degree from an accredited and internationally recognized medical school
  </li>
  <li>
   Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience
  </li>
  <li>
   Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process
  </li>
  <li>
   Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature
  </li>
  <li>
   Experience in Signal detection, Aggregate reports and Risk management.
  </li>
  <li>
   Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing
  </li>
  <li>
   Ability to establish and meet priorities, deadlines, and objectives
  </li>
  <li>
   Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs
  </li>
  <li>
   Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed
   <br/>
   <br/>
  </li>
 </ul>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
 <br/>
 <br/>
 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
</div>


American University in Cairo

<p><b>Position:</b> Senior Project Manager - ERP Project - Two-year project-based contract</p><p><b>Job Purpose: </b>The Senior Project Manager (SPM) leads the implementation of the University&rsquo;s ERP project. The role is accountable for planning, coordinating, and delivering the ERP project within agreed timelines and scope. Reporting to the ERP steering committee and project sponsor, i.e. president, the SPM ensures project governance, change management, and stakeholder engagement.</p><p>The SPM acts as the central coordinator between functional and technical stakeholders, and external vendors, ensuring strategic alignment and standards compliance, and ensuring the project delivers measurable institutional value and goals.</p><p><b>Core Responsibilities:</b></p><p>Project Management and Execution:</p><ul><li>Lead ERP implementation from initiation to post-go-live</li><li>Track progress and ensure delivery on time, scope, and budget</li><li>Develop and manage project plans, timelines, and risk registers</li><li>Identify risks and lead mitigation and quality control efforts</li><li>Coordinate activities across HR, finance, faculty affairs, IT, including the Senior Director, Tech Solutions ERP, and auxiliary units</li></ul><p>Change Management and Adoption of ERP project:</p><ul><li>Support change management in the ERP project</li><li>Develop communication plans, stakeholder engagement, and training programs</li></ul><p>Governance and Reporting:</p><ul><li>Executive Reporting: Provide structured updates, dashboards, and issue summaries to the ERP steering committee and project sponsor, i.e. president, in alignment with project phase reporting cycle</li><li>Decision Escalation: Identify and escalate critical decisions, scope changes, or risks requiring steering committee action</li><li>Project Governance: Ensure project decisions, risks, and changes are documented, tracked, and managed transparently</li></ul><p>Stakeholder Engagement:</p><ul><li>Liaison: Act as the central point of contact between the AUC project teams and external partners or vendors throughout implementation</li><li>Collaboration Facilitation: Lead workshops, gather business requirements, and ensure feedback loops are closed with clear actions</li><li>Institutional Alignment: Ensure that project outcomes are in service of project priorities, such as administrative efficiency and stakeholder experience</li></ul><p>Vendor and Partner Coordination:</p><ul><li>Implementation Oversight: Manage day-to-day activities of ERP implementation vendors and consultants to ensure timelines, deliverables, and quality standards are met</li><li>Contract Execution: Monitor service levels, escalate delivery risks, and coordinate corrective actions as needed</li><li>Project Integration: Ensure that third-party deliverables are tightly aligned with the ERP project plan</li></ul><p><b>Qualifications:</b></p><p><b>Education and Experience:</b></p><ul><li>Bachelor&rsquo;s degree in information systems, computer science, business administration, or related field</li><li>Master&rsquo;s degree is preferred</li><li>A minimum of 15 years of project management experience, with at least five years in ERP implementations with strong track record of successful ERP implementation</li><li>Experience in cloud-based ERP deployments and middleware integrations</li></ul><p><b>Skills:</b></p><p>Technical Domain Expertise:</p><ul><li>ERP Implementation: Hands-on experience leading ERP rollouts, e.g., Oracle Fusion, SAP S/4HANA in a complex environment</li><li>Project Management: Proficient in managing complex, cross-functional projects using methodologies like PMP, PRINCE2, and change management, Prosci or equivalent</li></ul><p>Higher Education Experience, Preferred:</p><ul><li>Familiarity with university structures, governance, and academic or administrative systems</li><li>Stakeholder Engagement: Strong ability to build consensus, lead workshops, and manage expectations across diverse groups</li><li>Vendor Relationship Management: Skilled in managing third-party vendors, contracts, and deliverables</li></ul><p><i>This position is open until filled.</i></p><p><i>Placement is based on the candidate&rsquo;s experience and skills. Only candidates who make it to the short list will be contacted.</i></p><p>&quot;The American University in Cairo is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Individuals with disabilities are encouraged to apply.&quot;</p><p><i><b>&ldquo;We thank all individuals who have expressed interest in working at The American University in Cairo.&rdquo;</b></i></p><p>Job Type: Contract<br/>Contract length: 24 months</p><p>Work Location: In person</p>

Senior Project Manager - ERP Project - Two-year project-based contract

Hilton

<div><p>Director of Human Resources</p><p>
A Director of Human Resources will manage Human Resources related activities including succession planning, talent management, recruitment, learning and development and training, performance management, compensation and benefits, and employee relations initiatives.</p><br>
<p><br>
<br>
<b>What will I be doing?</b></p><br>
<p>As a Director of Human Resources, you will be responsible for the effective management and performance of all Human Resources related activities. This includes talent management, succession planning, learning and development and training, performance management, compensation and benefits, employee relations, and health and safety initiatives. Specifically, a Director of Human Resources will perform the following tasks to the highest standards:</p>
<ul><li>Plan and forecast the short and long-term talent requirements for the hotel to support its business plans</li>
<li>Maintain a best practice recruitment approach, including the Company's vacancy management system, to attract the best applicants</li>
<li>Build a strong career and succession planning system to retain and develop talent</li>
<li>Implement training and development strategies to continuously improve performance and customer service</li>
<li>Oversee the hotel's human resources database and payroll system</li>
<li>Provide a framework for counseling, coaching, and welfare services</li>
<li>Manage the Opinion Survey and the calendar of Team Member social events</li>
<li>Manage and resolve, promptly and completely, all employee relations issues</li>
<li>Maintain an awareness of competitor human resources activities and best practices</li>
</ul><b>What are we looking for?</b><p><br>
A Director of Human Resources serving Hilton brands is always working on behalf of our Guests and working with other Team Members. To successfully fill this role, you should maintain the attitude, behaviours, skills, and values that follow:</p><ul>
<li>Tertiary qualifications, or other collegiate-level degree, in Human Resources or related field, required</li>
<li>Previous human resources management experience in the hotel, leisure, and/or retail sector</li>
<li>Excellent leadership skills and exceptional communication skills</li>
<li>Strong commercial/business acumen</li>
<li>A passion for leadership and the vision to create a winning team</li></ul><br>
<b>
What will it be like to work for Hilton?</b><br>
<p>Hilton is the leading global hospitality company, spanning the lodging sector from luxurious full-service hotels and resorts to extended-stay suites and mid-priced hotels. For nearly a century, Hilton has offered business and leisure travelers the finest in accommodations, service, amenities and value. Hilton is dedicated to continuing its tradition of providing exceptional guest experiences across its global brands. Our vision &ldquo;to fill the earth with the light and warmth of hospitality&rdquo; unites us as a team to create remarkable hospitality experiences around the world every day. And, our amazing Team Members are at the heart of it all!</p></div>

Director of Human Resources

Merck KGaA

<p></p><div><p>Work Your Magic with us!</p><p></p><p><br>
Ready to explore, break barriers, and discover more? We know you&rsquo;ve got big plans &ndash; so do we! Our colleagues across the globe love innovating with science and technology to enrich people&rsquo;s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.</p><p></p><p><br>
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.</p><p></p><p><b><br>
Your Role:
</b></p><p>Are you passionate about patient safety and looking to make a significant impact in the field of pharmacovigilance? An exciting opportunity has opened up with our company. We are looking to hire a Patient Safety Center Associate and Local Safety Responsible (LSR) for Egypt based locally in the country for the Patient Safety Center Africa.</p><p>
Responsibilities:</p><ul><li>
All Pharmacovigilance (PV) related tasks in Egypt where this role will be nominated as local Safety Responsible (LSR) to Egypt Health Authority.
</li><li>Collaborate with a team handling PV activity across other African countries. This is a unique opportunity to work cross-functionally at both local and global levels, driving initiatives that enhance patient safety.</li><li>
As a Patient Safety Center Associate, you will be an integral part of our regional organization, the Patient Safety Center Africa and will be responsible to ensure that individual case safety reports from the local market are appropriately processed and followed up.
</li><li>This role will be responsible for the establishment and maintenance of the marketing authorization holder &lsquo;s pharmacovigilance system while maintaining promoting and improving compliance with local regulatory requirements.</li><li>
Maintain the local PV documentation of the PV systems and perform PV training as applicable. You will contribute to local audits and inspections and will support the preparation of local Risk Management Plan and submission of local aggregate safety report where applicable.
</li><li>Monitor the local PV regulation and properly follow up on the generated activities.</li><li>
Uploading new information, updating records, necessary registrations and submissions to regulators systems with good understanding of Safety Databases.</li><li>
Implementation of PV agreements and perform the required PV activities related to Patient Data collection systems and Clinical studies.</li><li>
Collaborate closely with the Global Organizations as well as the cross-functional teams (local Management, QA, Medical Affairs, Regulatory Affairs Business Unit)</li></ul><p><b>
Who you are:
</b></p><ul><li>Bachelor Degree of Pharmacy or Medicine.</li><li>
Fluent in written and spoken local language and English.</li><li>
4/5 years in PV or in the pharma industry. Health authority experience is an advantage.</li><li>
Understand business needs, think strategically, and develop risk mitigation strategies.</li><li>
High level of dedication and a strong willingness to perform.</li><li>
You are curious, obsessed with customers and patients and act as the owner to make the right decision while keeping in mind the Company&rsquo;s best interests.</li></ul><p></p><p><b><br>
What we offer:</b> We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!</p><p></p><p><br>
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</p></div>

Patient Safety Center Associate Manager

Merck Healthcare

<div>
 Work Your Magic with us!
 <br/>
 <br/>
 Ready to explore, break barriers, and discover more? We know you&rsquo;ve got big plans &ndash; so do we! Our colleagues across the globe love innovating with science and technology to enrich people&rsquo;s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
 <br/>
 <br/>
 United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
 <br/>
 <br/>
 <strong>
  Your Role
  <br/>
  <br/>
 </strong>
 Are you passionate about patient safety and looking to make a significant impact in the field of pharmacovigilance? An exciting opportunity has opened up with our company. We are looking to hire a Patient Safety Center Associate and Local Safety Responsible (LSR) for Egypt based locally in the country for the Patient Safety Center Africa.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   All Pharmacovigilance (PV) related tasks in Egypt where this role will be nominated as local Safety Responsible (LSR) to Egypt Health Authority.
  </li>
  <li>
   Collaborate with a team handling PV activity across other African countries. This is a unique opportunity to work cross-functionally at both local and global levels, driving initiatives that enhance patient safety.
  </li>
  <li>
   As a Patient Safety Center Associate, you will be an integral part of our regional organization, the Patient Safety Center Africa and will be responsible to ensure that individual case safety reports from the local market are appropriately processed and followed up.
  </li>
  <li>
   This role will be responsible for the establishment and maintenance of the marketing authorization holder &lsquo;s pharmacovigilance system while maintaining promoting and improving compliance with local regulatory requirements.
  </li>
  <li>
   Maintain the local PV documentation of the PV systems and perform PV training as applicable. You will contribute to local audits and inspections and will support the preparation of local Risk Management Plan and submission of local aggregate safety report where applicable.
  </li>
  <li>
   Monitor the local PV regulation and properly follow up on the generated activities.
  </li>
  <li>
   Uploading new information, updating records, necessary registrations and submissions to regulators systems with good understanding of Safety Databases.
  </li>
  <li>
   Implementation of PV agreements and perform the required PV activities related to Patient Data collection systems and Clinical studies.
  </li>
  <li>
   Collaborate closely with the Global Organizations as well as the cross-functional teams (local Management, QA, Medical Affairs, Regulatory Affairs Business Unit)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Who You Are
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor Degree of Pharmacy or Medicine.
  </li>
  <li>
   Fluent in written and spoken local language and English.
  </li>
  <li>
   4/5 years in PV or in the pharma industry. Health authority experience is an advantage.
  </li>
  <li>
   Understand business needs, think strategically, and develop risk mitigation strategies.
  </li>
  <li>
   High level of dedication and a strong willingness to perform.
  </li>
  <li>
   You are curious, obsessed with customers and patients and act as the owner to make the right decision while keeping in mind the Company&rsquo;s best interests.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What we offer:
 </strong>
 We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 <br/>
 <br/>
 Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
</div>


Caduceus Lane

<p><b>Job Overview</b><br/>We are seeking a dynamic and proactive Event Management Associate to join our vibrant team in a commercial role dedicated to orchestrating exceptional events. In this role, you will be the driving force behind planning, coordinating, and executing a wide range of events that elevate our brand presence and foster meaningful client relationships. Your energetic approach and meticulous organizational skills will ensure each event is executed flawlessly, delivering memorable experiences that align with our strategic objectives. This paid position offers an exciting opportunity to develop your expertise in event marketing, hospitality, and client engagement within a fast-paced environment.</p><p><b>Duties</b></p><p>The Event Management Associate position is a full-time, on-site role located in Cairo, Egypt.</p><p>Strategic Commercial Associate serves as the primary liaison between key pharmaceutical partners and internal cross-functional teams. dedicated to transforming complex brand visions into high-impact physical and digital experiences at premier medical congresses and scientific exhibitions. complete Event Life Cycle&mdash;from initial conceptualization to onsite execution. A core focus of the position is identifying and integrating emerging healthcare exhibition technologies to provide innovative, market-leading solutions that differentiate clients from their competitors.</p><p>Monitor the competitive profile of our clients&rsquo; therapeutic areas during events to provide &quot;Field Intelligence&quot; reports after the exhibition.</p><p>Implement commercial tactics to meet quantitative and qualitative targets.</p><p>Forecast key metrics, track account progress, and identify new growth opportunities within your portfolio.</p><p>Planning and managing events, coordinating with clients and stakeholders, and ensuring smooth execution of all event-related activities.</p><p>Involves providing excellent customer service, crafting event proposals, maintaining vendor relationships, and executing sales strategies to secure and deliver successful events.</p><p><b>Experience</b></p><ul><li>7+ years of experience in Commercial/Sales Role With multiple Event Leadership Execution.</li></ul><p>Bachelor&rsquo;s degree in Pharmacy or an equivalent medical degree.</p><p>Exceptional public speaker with a proven ability to influence and negotiate at the executive level.</p><p>A &quot;can-do&quot; attitude with the ability to thrive in a fast-paced, matrix environment.</p><p>Fluency in English is a must.</p><p>Analytical, self-motivated, and ready to win</p><p>Excellent Communication and Customer Service skills for client interactions and stakeholder management</p><p>Experience in Sales with a proven ability to cultivate and maintain client relationships</p><p>Strong organizational and time management skills, with attention to detail</p><p>Ability to work in a fast-paced environment and meet deadlines</p><p>Prior experience in event management or related fields is a plus</p><p>Job Type: Full-time</p><p>Pay: E&pound;20,000.00 - E&pound;30,000.00 per year</p>

Event Management Associate -Commercial Role

Explore 936+ Associate medical safety director sponsor dedicated in Egypt this March. Find roles across top companies and apply now to boost your career.

936 associate medical safety director sponsor dedicated jobs In Egypt

Associate Medical Safety Director- Sponsor Dedicated

Associate Medical Safety Director- Sponsor Dedicated

Senior Project Manager - ERP Project - Two-year project-based contract

Director of Human Resources

Patient Safety Center Associate Manager

Patient Safety Center Associate Manager

Event Management Associate -Commercial Role