Urwah Admin

IQVIA

<div>
 <em>
  <strong>
   This Role is based in Jeddah.
   <br/>
   <br/>
  </strong>
 </em>
 <em>
  <strong>
   Contract Duration - 1 year.
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  </strong>
 </em>
 <strong>
  Position Overview
  <br/>
  <br/>
 </strong>
 We are looking for a highly organized and proactive
 <strong>
  Event, Logistics, and Governance Coordinator
 </strong>
 to handle the planning, execution, and management of events, logistics, and governance processes.
 <br/>
 <br/>
 The ideal candidate will ensure compliance, maintain data accuracy, and provide system support for tools like
 <strong>
  IHub (Compliance System)
 </strong>
 and
 <strong>
  LEAN/Ariba (Purchasing System)
 </strong>
 .
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 <br/>
 This role also involves generating reports, analyzing data, ensuring smooth operations across multiple functions, and stepping in to support team operations in the absence of other team members when necessary.
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 <strong>
  Key Responsibilities
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  <br/>
 </strong>
 <ul>
  <li>
   Event and Logistics Management
  </li>
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   Plan and support the execution of internal and external events, meetings, and activities, including budgeting, documentation, and adherence to procurement policies.
  </li>
  <li>
   Organize events with budgets, ensuring all logistics such as venue selection, catering, transportation, and accommodation are handled efficiently.
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   Coordinate with vendors to secure cost-effective rates and ensure timely delivery of services.
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   Manage event registration and attendance, including logistics for international congresses and local standalone activities.
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   Collaborate with marketing and medical teams to align event activities with strategic objectives.
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   Governance and Compliance
  </li>
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   Utilize the IHub system to manage timely data entry as per policy requirements.
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   Perform quarterly quality checks in IHub to ensure data accuracy and compliance.
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   Attend training sessions and support team members with system-related inquiries as a super-user.
  </li>
  <li>
   Manage Purchase Requests (PRs) and Service Entry Sheets (SES) for assigned activities.
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   Ensure the timely creation, follow-up, and closure of PRs and SES for both planned and ad-hoc activities.
  </li>
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   Oversee monthly and annual accrual processes, ensuring timely closures.
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   Ensure payments are processed on time and in compliance with procurement policies and guidelines.
  </li>
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   Reporting and Data Analysis
  </li>
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   Generate detailed reports on event budgets, vendor performance, and payment statuses.
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   Analyze data to identify trends, evaluate event performance, and recommend process improvements.
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   Provide actionable insights to stakeholders based on event and governance data.
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   Monitor key performance indicators (KPIs) to ensure objectives are being met.
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   Documentation and Continuous Improvement
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   Maintain accurate records and files for all events, governance processes, and compliance activities.
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   Conduct periodic reviews of open interactions in IHub and ensure closure every two months.
  </li>
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   Collect and analyze feedback from team members and event attendees to enhance future activities.
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   Identify and implement process improvements to streamline event and governance workflows.
  </li>
  <li>
   Step in to manage tasks and responsibilities in the absence of other team members, ensuring seamless operations.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Event Management: Ability to coordinate complex events with high attention to detail.
  </li>
  <li>
   System Expertise: Proficiency in using tools like IHub, LEAN, and Ariba for data entry, governance, and procurement processes.
  </li>
  <li>
   Data Management: Strong skills in ensuring data accuracy and maintaining high-quality deliverables.
  </li>
  <li>
   Reporting and Analytics: Experience in generating reports and analyzing data to improve performance.
  </li>
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   Time Management: Ability to handle multiple tasks, meet deadlines, and follow up on processes efficiently.
  </li>
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   Communication and Collaboration: Strong verbal and written communication skills to work effectively with cross-functional teams.
  </li>
  <li>
   Adaptability: Willingness to take on additional responsibilities and manage tasks in the absence of other team members.
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   <br/>
  </li>
 </ul>
 <strong>
  Required Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience in event coordination, governance processes, or a related role.
  </li>
  <li>
   Familiarity with PR creation, SES management, and accrual processes.
  </li>
  <li>
   Experience with medical or marketing event coordination is a plus.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Indicators of Success
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Smooth execution of events and logistics with positive feedback from stakeholders.
  </li>
  <li>
   Timely and accurate creation and closure of PRs, SES, and accruals.
  </li>
  <li>
   High-quality data entry and compliance with governance processes.
  </li>
  <li>
   Effective vendor management and cost optimization.
  </li>
  <li>
   Consistent performance in maintaining operations during team member absences.
   <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
</div>


Event, Logistics, and Governance Coordinator - (Jeddah)

<div>
 The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular clinical innovation, is looking for exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development.
 <br/>
 <br/>
 The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA.
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 <br/>
 The key remit of the role is drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials.
 <br/>
 <br/>
 The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly Phases 1-3. The Medical Strategy Lead will also be responsible for early engagement business development activities, providing scientific knowledge and expertise to guide sponsors in Cardiovascular development.
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 <br/>
 As a subject matter expert, the Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.
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 <br/>
 <strong>
  Responsibilities
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  <br/>
 </strong>
 <ul>
  <li>
   Accountable and responsible for creating innovative, evidence-based, and patient-centered delivery strategies and solutions for Cardiovascular pre-approval clinical trials or studies, addressing the specific needs and challenges of each customer.
  </li>
  <li>
   In partnership with Indication-Specific Medical Strategy, Operations, Sales, and other functions, responsible for award of strategic and tactical new business to achieve annual Gross New Business targets. Responsible for the inclusion of Cardiovascular elements into proposals.
  </li>
  <li>
   Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
  </li>
  <li>
   Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required.
  </li>
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   Participates in strategic business development activities including presentations to prospective clients and professional meetings.
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   Maintains awareness of industry pipeline and scientific and business landscape; supports due diligence research of the Cardiovascular landscape.
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  </li>
 </ul>
 <strong>
  Requirements
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  <br/>
 </strong>
 <em>
  Scientific and Research Qualifications and Experience
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 </em>
 <ul>
  <li>
   Cardiologist. A degree from an accredited and internationally recognized school is required
  </li>
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   2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience
  </li>
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   Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular
  </li>
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   Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
  </li>
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   In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  </li>
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   Demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall offering
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   Strong clinical research skills and commitment to evidence-based and patient-centered clinical development
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  </li>
 </ul>
 <em>
  Professional Skills
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 </em>
 <ul>
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   Excellent communication, presentation and interpersonal skills, including good command of English language (both written and spoken)
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   Strong leadership skills, ability to work with minimal supervision, and lead a virtual team in a matrix organization
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   Innovative and strategic thinker
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   Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in both sales and operational environments
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   Flexible and able to work in situations where specifications may or may not be well defined and willing to support work in other therapeutic areas when required
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   Confident and capable in the use of technology, applications and other media e.g. databases and internet to research assess new opportunities, maintain currency of therapeutic and operational knowledge and competitive landscape.
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   Proven ability to make decisions with limited information, bringing clarity to disparate information to inform actions and drive results
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  </li>
 </ul>
 <em>
  Interpersonal Skills
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 </em>
 <ul>
  <li>
   Ability to establish and maintain effective working relationships with co-workers, managers and clients. Maintains a positive outlook at work; handles criticism well and learns from it
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   Ability to establish and maintain effective working relationships with a wide network of individuals e.g. co-workers, managers and customers
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   Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues
   <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
</div>


Senior Director, Medical Strategy Lead- Cardiologist

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Hybrid | R1521941</div></div><p></p><div><div><b><br>
Join Us on Our Journey to Reimagine Healthcare!</b></div><div>
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. With 85,000 employees across more than 100 countries, we create intelligent connections across the healthcare ecosystem through data, transformative technology, and deep industry expertise.</div><div>
We are now looking for a <b>Key Account Manager</b> to join our Sales team and support pharmaceutical clients in their growth strategies by leveraging IQVIA&rsquo;s data assets and services.</div><div><b>
Role Summary</b></div><div>
As a Key Account Manager, you will build and <b>nurture client relationships</b>, <b>drive revenue growth</b>, and identify <b>new business opportunities</b> across your assigned accounts. You will be the primary point of contact for strategic clients, ensuring they maximize the value of IQVIA&rsquo;s solutions.</div><div><b>
Key Responsibilities:</b></div><div><b><i>
Client Engagement &amp; Business Understanding</i></b></div><ul><li>
Build, strengthen, and expand relationships across client organizations, especially with top strategic accounts.</li><li>
Promote IQVIA products and services to achieve revenue targets.</li><li>
Develop a deep understanding of client priorities and translate them into actionable business opportunities.</li><li>
Create and execute strategic account plans.</li><li>
Act as a trusted advisor on marketing, market research, sales management, industry trends, and IQVIA capabilities.</li></ul><div><b><i>
Commercial &amp; Operational Excellence</i></b></div><ul><li>
Manage contract renewals, subscriptions, and commercial performance metrics.</li><li>
Oversee internal and external financial processes (rebates, invoicing, accounts receivable, DSO).</li><li>
Maintain visibility on pipeline, recent wins, and strategic opportunities (keeping CRM systems updated with opportunities, activities, and account plans).</li><li>
Ensure high levels of client satisfaction in partnership with Client Service teams.</li></ul><div><b><i>
Strategic Client Development</i></b></div><ul><li>
Shape client perception by sharing relevant marketing materials and thought leadership.</li><li>
Facilitate peer-to-peer engagement by connecting clients with relevant IQVIA experts.</li><li>
Identify innovation opportunities aligned with client priorities and IQVIA&rsquo;s strategic direction.</li><li>
Contribute to the broader Sales &amp; Account Management community by sharing insights and best practices.</li></ul><div><b><i>
Skills, Experience &amp; Qualifications</i></b></div><ul><li>
Minimum 4 years of experience in Sales and/or Business Development within the pharmaceutical industry.</li><li>
Strong interpersonal skills and ability to build long-term business relationships.</li><li>
Proven negotiation and influencing capabilities.</li><li>
Demonstrated proactivity and ability to identify and convert opportunities.</li><li>
Solid understanding of the pharma business model and life sciences commercial strategy.</li><li>
Experience working successfully in a matrixed organization.</li><li>
Excellent customer service mindset and ability to translate client needs into solutions.</li><li>
Confidence in contractual and procurement processes.</li><li>
Strong judgment and decision-making skills.</li><li>
Minimum Bachelor degree in Engineering, Business Management, or related field.</li><li>
Fluency in English.</li></ul><div>
Please submit your CV in English</div><div><b><i>
Why Join IQVIA?</i></b></div><div>
At IQVIA, you can shape your career and choose the path that best supports your growth. With exposure to diverse geographies, capabilities, and therapeutic areas, you&rsquo;ll find endless opportunities to learn, evolve, and make an impact.</div><div>
We believe that meaningful results come from the right people working in the right environment. Here, you&rsquo;ll help clients drive healthcare forward and ultimately improve human health outcomes.</div><div>
It&rsquo;s an exciting time to join us &mdash; and to reimagine what&rsquo;s possible in healthcare.</div><div>
Moving healthcare forward. Together.</div><div>
IQVIA is committed to fostering a diverse and inclusive workplace. We believe that embracing diversity strengthens our teams, enhances innovation, and enables every employee to reach their full potential.</div><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></div><div></div>

Key Account Manager - Istanbul based

<div><div><div>Thane, India | Full time | Home-based | R1518189</div></div><p></p><div><div><br>
&quot;&bull; Minimum 4 years clinical study database development experience in the pharmaceutical industry
<br>
<ul><li>Minimum of 3 years hands on Rave study build experience, including module connections such as Safety Gateway and TSDV</li><li>Bachelor's degree required
</li><li>Thorough understanding of regulations, GCP, ICH Guidelines as they apply to creation and maintenance of clinical study databases</li><li>Good ability to communicate with study team members, plan/organize work to deliver against timelines&quot;</li></ul></div><div>
&quot;&bull; Build studies for initial deployment and protocol amendments and/or oversee CROs and quality check their work (includes forms, database structures, cleaning edit checks).<br>
<ul><li>Program study database integrations (TSDV, CCV, TMS, Safety Gateway)</li><li>Work with Data Management/Study teams to plan for build timelines, develop database/edit check specifications, migration content, and migration plans; resolve issues and re-plan as needed</li><li>Serve as a primary database build point of contact for assigned studies and provide support during study execution and closure</li><li>For database changes after initial deployment - perform impact analysis, create test migration plan, execute migration test, and deploy changes into production
</li><li>Support troubleshooting of technical issues, working with other internal groups and with Medidata as needed</li><li>Provide technical support for continuous improvement efforts and audit support (study specific)
</li><li>Build database components at the global level as needed</li></ul>
&quot;</div><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></div><div></div>

Database Management Specialist

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Home-based | R1522619</div></div><p></p><div><div><br>
Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and scientific information with healthcare providers and caregivers. <b>This is a fixed-term opportunity for 12-months contract.</b></div><h3 class="jobSectionHeader"><b>
Essential Functions</b></h3><ul><li><div>
Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training</div></li><li><div>
Provides education to healthcare professionals and their staff, reinforcing study protocols as related to a clinical trial</div></li><li><div>
May partner with referral networks to identify potential subjects for a trial</div></li><li><div>
Maintains and analyzes customer records to customize strategies to maximize pre-screening, screening, and enrollment in trials</div></li><li><div>
Completes internal electronic reporting systems; organizes and holds group events to optimize program delivery</div></li><li><div>
Successfully manages objections raised</div></li><li><div>
Maintains up-to-date technical knowledge of specialty and disease areas</div></li></ul><h3 class="jobSectionHeader"><b>
Qualifications</b></h3><ul><li><div>
Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications</div></li><li><div>
Registered Nurse or CRA experience is required</div></li><li><div>
1&ndash;2 years of prior relevant experience</div></li><li><div>
High flexibility to travel (internationally, if needed)</div></li><li><div>
Clinical competence in relevant therapeutic area</div></li><li><div>
Excellent interpersonal and communication skills</div></li><li><div>
Strong written and verbal communication skills, including good command of English</div></li><li><div>
Ability to execute tasks with minimal oversight</div></li><li><div>
Ability to coordinate and complete activities across multiple functions</div></li><li><div>
Solutions-based approach to problem-solving</div></li><li><div>
Positive, can-do attitude</div></li><li><div>
Strong customer service orientation</div></li><li><div>
Collaborative mindset and team player</div></li><li><div>
Demonstrates empathy and awareness of cultural differences</div></li><li><div>
Upholds the values of IQVIA and the CTE group</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></div><div></div>

Clinical Trial Educator

<div>
 Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and scientific information with healthcare providers and caregivers.
 <strong>
  This is a fixed-term opportunity for 12-months contract.
  <br/>
  <br/>
 </strong>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training
  </li>
  <li>
   Provides education to healthcare professionals and their staff, reinforcing study protocols as related to a clinical trial
  </li>
  <li>
   May partner with referral networks to identify potential subjects for a trial
  </li>
  <li>
   Maintains and analyzes customer records to customize strategies to maximize pre-screening, screening, and enrollment in trials
  </li>
  <li>
   Completes internal electronic reporting systems; organizes and holds group events to optimize program delivery
  </li>
  <li>
   Successfully manages objections raised
  </li>
  <li>
   Maintains up-to-date technical knowledge of specialty and disease areas
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications
  </li>
  <li>
   Registered Nurse or CRA experience is required
  </li>
  <li>
   1&ndash;2 years of prior relevant experience
  </li>
  <li>
   High flexibility to travel (internationally, if needed)
  </li>
  <li>
   Clinical competence in relevant therapeutic area
  </li>
  <li>
   Excellent interpersonal and communication skills
  </li>
  <li>
   Strong written and verbal communication skills, including good command of English
  </li>
  <li>
   Ability to execute tasks with minimal oversight
  </li>
  <li>
   Ability to coordinate and complete activities across multiple functions
  </li>
  <li>
   Solutions-based approach to problem-solving
  </li>
  <li>
   Positive, can-do attitude
  </li>
  <li>
   Strong customer service orientation
  </li>
  <li>
   Collaborative mindset and team player
  </li>
  <li>
   Demonstrates empathy and awareness of cultural differences
  </li>
  <li>
   Upholds the values of IQVIA and the CTE group
   <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
</div>


<div><div><div>Riyadh, Saudi Arabia | Full time | Hybrid | R1521758</div></div><p></p><div><div><br>
Job Overview</div><div><br>
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.<br>
<br>
Essential Functions</div><div><ul><li><br>
Provide clinical research support to investigators to prepare for and execute assigned research studies, including:</li><li>Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data</li><li>Attend all relevant study meetings</li><li>Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research</li><li>Recruit and screen patients for clinical trials and maintain subject screening logs</li><li>Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits</li><li>Design and maintain source documentation based on protocol requirements</li><li>Schedule and execute study visits and perform study procedures</li><li>Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness</li><li>Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics</li><li>Monitor subject safety and report adverse reactions to appropriate medical personnel</li><li>Correspond with research subjects and troubleshoot study-related questions or issues</li><li>Participate in &ldquo;huddles&rdquo; to confirm daily study tasks are assigned to team members and are executed to the expected standards</li><li>Assist with study data quality checking and query resolution.</li><li>Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.</li><li>Record, report and interpret study findings appropriately to develop a study-specific database.</li><li>Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.</li><li>Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.</li><li>Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.</li><li>Assist research site with coverage planning related to staffing and scheduling for research projects.</li></ul><br>
Qualifications</div><div><ul><li><br>
Bachelor's Degree</li><li>3 years&rsquo; relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience</li></ul></div><ul><li>Working knowledge of clinical trials</li><li>Working knowledge of the principles of Good Clinical Practices (GCP)</li><li>In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules</li><li>Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing</li><li>Good skill in using MS Windows and Office applications such as Access, Outlook and Word</li><li>Excellent interpersonal skills</li><li>Ability to pay close attention to detail</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients</li><li>Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies</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></div><div></div>

Clinical Site Coordinator

Join IQVIA and explore 16   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.

IQVIA

ABOUT_COMPANY

Event, Logistics, and Governance Coordinator - (Jeddah)

Senior Director, Medical Strategy Lead- Cardiologist

Key Account Manager - Istanbul based

Database Management Specialist

Clinical Trial Educator

Clinical Trial Educator

Clinical Site Coordinator