Urwah Admin

IQVIA

<div><div><div>Doha, Qatar | Full time | Hybrid | R1479501</div></div><p></p><div><h2 class="jobSectionHeader"><b><br>
Role Purpose:</b></h2><div><h2 class="jobSectionHeader"><b>
The role is part of a dedicated team of finance and patient activity experts supporting Consultant and Senior Consultants in designing, configuring and supporting of Patient Level Information Costing System(PLICS) and health pathway analytical software solutions using the company's own web-based applications along with third party proprietary Business Intelligence tools.
</b></h2><h2 class="jobSectionHeader"><b>An ability to work to tight deadlines within a cross-functional team to achieve project delivery success is required, together with strong written and verbal communication skills. Candidates should be able to show an understanding of the Healthcare business relevance in the analyses as well as their correct and effective execution.</b></h2><h2 class="jobSectionHeader"><b>
Principle Accountabilities:</b></h2><div><ul><li><h2 class="jobSectionHeader"><b>
Support the Senior Consultant in the design, development and delivery of PLICS and Pathways Analytics consulting projects or as components of larger, complex projects.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Participates in the active development of Software products.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Support the Consultant/Senior Consultant in reviewing and analyzes client requirements or problems and assists in the development of approaches and system configurations to provide cost effective solutions that ensure profitability and high client satisfaction.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Support the Consultant/Senior Consultant in conducting Financial and Costing Consultancy in the Healthcare sector</b></h2></li><li><h2 class="jobSectionHeader"><b>
Thorough knowledge on the patient activity data flow process within a hospital.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Be able to performs qualitative and/or quantitative analyses to assist in the identification of client issues and the development of client specific solutions.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Support the Senior Consultant in recommending improvements and alternative solutions to resolve problems.</b></h2></li><li><h2 class="jobSectionHeader"><b>
May identify new business opportunities of follow-on work and new leads at assigned client.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Provides follow-up with client after project deliverable has been completed to ensure client satisfaction.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Needs to have a good understanding of Financial and Management Accounting experience.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Needs to have a good understanding of International Financial Reporting Standards (IFRS).</b></h2></li><li><h2 class="jobSectionHeader"><b>
Understanding of how Costing fits into the Payer Provider portfolio.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Needs to have or develop good understanding of SQL.</b></h2></li></ul></div></div><h2 class="jobSectionHeader"><b>
Education, Experience, &amp; Specialized Knowledge Required:</b></h2><div><h2 class="jobSectionHeader"><b>
Essential: </b><b>Bachelor&rsquo;s degree in Finance or Accountancy with 1&ndash;3 years of finance experience. </b><b>Preferred: </b><b>Costing experience is preferred and professional qualifications like CMA,ACA, ACCA and CIMA will be given preference.</b></h2></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>
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>

Senior Consultant - ( Patient Level Information Costing System)

<div><div><div>San Antonio, United States of America | Full time | Home-based | R1524464</div></div><p></p><div><div><b><br>
Job Summary
</b></div><div>The Research Compliance Coordinator must be knowledgeable of standard research and oncology care practices. The Research Compliance Coordinator advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.</div><div><b>
Essential Duties and Responsibilities</b></div><div>
Essential and other important responsibilities and duties may include but are not limited to the</div><div>
following:</div><div><b>
Protocol Compliance</b></div><ul><li>Reviews and comprehends the research protocol</li><li>Adheres to applicable federal, state, and institutional regulations, policies, and procedures</li></ul><div>
related to clinical research</div><ul><li>Complies with NEXT Oncology SOPs</li><li>Develops and maintains source documents, templates, or forms in a timely fashion.</li><li>Ensure all protocol requirements have been captured on site specific forms, documents,</li></ul><div>
or templates.</div><ul><li>Assesses protocol for discrepancies or questions to ensure accurate source documents</li></ul><div>
and forms are created</div><ul><li>Assess and update forms for protocol amendments or protocol clarification letters</li><li>Assess and update forms when issues are identified during the course of patient</li></ul><div>
treatments</div><ul><li>Participates in quality control activities to ensure data integrity, including timely</li></ul><div>
responses to database or sponsor queries</div><ul><li>Provide monthly reports to team to ensure compliance with protocol specified task</li></ul><div><b>
Knowledge, Skills and Abilities</b></div><ul><li>Bilingual in English/Spanish, preferred</li><li>Knowledge of appropriate software including Microsoft Word, Excel, and Outlook,</li></ul><div>
Microsoft PowerPoint and Adobe Acrobat</div><ul><li>Attention to detail, organizational and accuracy skills</li></ul><div><b>
Required Education and Experience</b></div><ul><li>Current State Registered Nursing License for RNs</li><li>Bachelor&rsquo;s degree required for non-RNs</li><li>Oncology clinical trial experience preferred</li></ul><div><b>
Why Join Us?</b></div><div>
At NEXT Oncology (an Avacare Business), you&rsquo;ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.</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>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</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>
The potential base pay range for this role, when annualized, is $47,400.00 - $118,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Research Compliance Coordinator

<div><div><div>San Antonio, United States of America | Full time | Office-based | R1528582</div></div><p></p><div><h3 class="jobSectionHeader"><b><br>
Job Overview</b></h3><div>
The Medical Laboratory Scientist performs high‑complexity clinical laboratory testing to support patient care and clinical research activities. This role applies professional and technical expertise to generate accurate, timely, and reliable laboratory results in areas such as hematology, chemistry, immunology, and specialized testing. Work is performed in accordance with CLIA regulations, CAP standards, Good Clinical Laboratory Practice (GCLP), and applicable quality and safety requirements.</div><h2 class="jobSectionHeader"><b>
Essential Functions</b></h2><ul><li>
Performs and reports high‑complexity laboratory tests, both automated and manual, with minimal supervision.</li><li>
Demonstrates competency in laboratory principles, methodologies, and instrumentation across assigned testing areas.</li><li>
Maintains adequate inventory of reagents and supplies and prepares reagents as required.</li><li>
Identifies and reports irregularities, instrument issues, or factors that may affect test accuracy.</li><li>
Participates in assay validation, method improvements, and implementation of new technologies.</li><li>
Follows all safety procedures, uses required personal protective equipment, and reports safety concerns.</li><li>
Ensures compliance with CLIA, CAP, GCLP, and internal quality management systems.</li><li>
Adheres to quality control policies, documents QC activities, and maintains a clean, organized work environment.</li><li>
Maintains required training, competency assessments, and continuing education.</li><li>
Supports internal and external audits, inspections, and quality initiatives.</li><li>
Verifies quality control results and releases patient or study results in accordance with regulatory requirements.</li><li>
Assists with training and onboarding of laboratory personnel as needed.</li><li>
Performs duties in alignment with ICH E6 Good Clinical Practice guidelines when supporting clinical trials.</li><li>
Participates in special projects and performs additional tasks assigned by laboratory leadership.</li></ul><h2 class="jobSectionHeader"><b>
Qualifications</b></h2><ul><li>
Bachelor&rsquo;s degree in Medical Laboratory Science, Biology, Chemistry, or a related field.</li><li>
0&ndash;5 years of clinical laboratory experience.</li><li>
Meets CLIA requirements for high‑complexity testing personnel.</li><li>
National certification as MLS/MT (ASCP, AMT, or equivalent) required.</li><li>
Strong understanding of laboratory principles, testing methodologies, and regulatory standards.</li><li>
Proficiency in laboratory safety, infection control, and handling of hazardous chemicals.</li><li>
Ability to perform complex calculations, including averages, standard deviations, and QC metrics.</li><li>
Skilled in troubleshooting laboratory instruments and resolving testing issues.</li><li>
Proficient with Microsoft Excel, Word, and PowerPoint.</li><li>
Strong organizational, interpersonal, and communication skills.</li><li>
Ability to manage multiple tasks with accuracy and attention to detail.</li><li>
Ability to work effectively with colleagues, management, and external partners.</li></ul><h2 class="jobSectionHeader"><b>
Equal Employment Opportunity</b></h2><div>
The company is an Equal Opportunity Employer and does not discriminate based on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected characteristic.</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>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</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>
The potential base pay range for this role, when annualized, is $46,200.00 - $96,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Medical Laboratory Scientist

<div><div><div>Istanbul, Turkey | Full time | Home-based | R1528167</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><h2 class="jobSectionHeader"><b><br>
Use your scientific and foreign language expertise to join the world&rsquo;s leading comprehensive pharmaceutical safety services organization at on a fast-growing team performing medical information call center services. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to ultimately provide oversight on projects and teams.
</b></h2><h2 class="jobSectionHeader"><b>RESPONSIBILITIES</b></h2><ul><li><h2 class="jobSectionHeader"><b>
Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Receive, triage, review and process Lifecycle safety operational data. Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Establish and maintain effective team project service operations communications
</b></h2></li><li><h2 class="jobSectionHeader"><b>Liaise with Project Manager by proactively identifying issues and proposing solutions</b></h2></li><li><h2 class="jobSectionHeader"><b>
Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives</b></h2></li></ul><h2 class="jobSectionHeader"><b>
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES</b></h2><ul><li><h2 class="jobSectionHeader"><b>
Life Sciences Degree</b></h2></li><li><h2 class="jobSectionHeader"><b>
Excellent written and verbal skills in Lithuanian, </b><b>English and other foreign language.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Excellent attention to detail and accuracy maintaining consistently high-quality standards.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Excellent organizational skills and time management skills.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Ability to establish and maintain effective working relationships with coworkers, managers and clients.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.</b></h2></li></ul><h3 class="jobSectionHeader"><b>
This role is not available for UK visa sponsorship</b></h3><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>

Medical Information and Adverse Event Intake Specialist with Lithuanian, English and additional foreign language

<div><div><div>Nashville, United States of America | Full time | Field-based | R1530418</div></div><p></p><div><div><br>
Key Account Representative</div><div><b>
In partnership with our client, we are actively searching for Key Account Representatives to deliver on our commitment to serve patients. The Key Account Representative will be responsible for promoting a product to specialty healthcare providers in an assigned territory.</b></div><div><b>
Qualifications/Experience:</b></div><div>
4-year degree from an accredited college or university required</div><div>
2 years B2B sales experience preferred</div><div>
1 year of pharmaceutical or med device sales experience a plus</div><div>
Device or diagnostic experience a plus</div><div>
Documented sales performance (top 10% or Presidents Club)</div><div>
Proven track record of exceeding sales objectives</div><div>
Following experience a plus:</div><ul><li>
Military</li><li>
Experience during college<ul><li>
Work/internship</li><li>
Competitive sport</li><li>
Leadership</li></ul></li></ul><div>
Have a valid driver&rsquo;s license and be insurable</div><div>
25% travel may be required</div><div>
May need to work evenings and weekends as needed (conferences, programs)</div><div><b>
Requirements:</b></div><ul><li>
Entrepreneurial spirit and drive</li><li>
Demonstrated business acumen</li><li>
Demonstrated analytical skills</li><li>
Demonstrated success in persuasion, influence, and negotiation skills</li><li>
Demonstrated leadership ability</li><li>
Demonstrated ability to apply technical/scientific knowledge</li><li>
Flexibility to learn new products over time</li><li>
Knowledge of and experience with the selling process</li><li>
Initiative and execution-oriented</li><li>
Teamwork</li></ul><div>
#LI-CES</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>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</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>
The potential base pay range for this role is 80,000-85,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Key Account Representative, Nashville, TN

<div><div><div>Durham, United States of America | Full time | Home-based | R1530384</div></div><p></p><div><div><div><b><br>
Job Overview</b></div><br>
Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.</div><div><div><div><div><div><div><div><div><div><div><b>
Essential Functions</b><br>
<ul><li>Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory &amp; Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations</li><li>identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information. May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews.</li></ul></div><div><b>
Qualifications</b><br>
<ul><li>Bachelor's Degree Life sciences or related field Req</li><li>7 years&rsquo; relevant experience in a scientific or clinical environment including demonstrable experience in an international role. Equivalent combination of education, training and experience.</li><li>Strong negotiation and communication skills with ability to challenge</li><li>Excellent interpersonal skills and strong team player</li><li>Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects</li><li>Thorough understanding of regulated clinical trial environment and in depth knowledge of drug development process</li><li>Demonstrated proficiency in using systems and technology to achieve work objectives</li><li>Good regulatory and/or technical writing skills</li><li>Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines</li><li>Good leadership skills, with ability to motivate, coach and mentor</li><li>Good organizational and planning skills</li><li>Ability to exercise independent judgment taking calculated risks when making decisions</li><li>Good presentation skills</li><li>Proven ability to establish and maintain effective working relationships with co-workers, managers and sponsors.</li><li>Excellent understanding of study financial management</li><li>Proven ability to work on multiple projects balancing competing priorities</li></ul></div></div></div></div></div></div></div></div></div></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>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</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>
The potential base pay range for this role, when annualized, is $74,600.00 - $216,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

FSP Sponsor Dedicated - Study Start-Up Manager

<div><div><div>Cleveland, United States of America | Full time | Office-based | R1528571</div></div><p></p><div><div><br>
Fathom&rsquo;s <b>Associate Development Program</b> is a paid, high-impact summer experience designed to develop future digital marketing leaders.</div><div>
We&rsquo;re looking for motivated, curious, and team-oriented college students in the Cleveland area who want hands-on experience in paid media, SEO, and marketing automation&mdash;while being mentored by some of the best in the industry.</div><div>
As a Digital Marketing Associate, you&rsquo;ll play an active role in building and optimizing campaigns, uncovering insights that drive client outcomes, and contributing to the culture that makes Fathom a top Workplace in Northeast Ohio.</div><div><b>
What You&rsquo;ll Do (Responsibilities)</b></div><div><b>
Support Client Work &amp; Campaign Excellence</b></div><ul><li>
Participate in internal and external strategy discussions with cross-functional teams.</li><li>
Support the launch, QA, and ongoing optimization of digital campaigns across paid media, SEO, and marketing automation.</li><li>
Conduct channel, content, and competitive audits to uncover opportunities for performance improvement.</li><li>
Analyze campaign performance data and connect insights to client business objectives and KPIs.</li><li>
Assist in the development and implementation of testing strategies (A/B tests, messaging, targeting, landing pages).</li>
Document findings clearly and present recommendations to team members and mentors.<br>
<li>
</li></ul><div><b>Learn, Grow &amp; Contribute</b></div><ul><li>
Engage in structured learning sessions on digital marketing, analytics, healthcare marketing, and client success.</li><li>
Contribute positively to our team culture&mdash;collaboration, curiosity, and commitment to excellence.</li>
Demonstrate strong attention to detail and consistently deliver error-free work.<br>
<li>
</li></ul><div><b>What We&rsquo;re Looking For (Requirements)</b><br>
You might be a great fit if you:</div><ul><li>
Are currently pursuing a degree in Marketing, Business, Communications, Advertising, Analytics, or a related field.</li><li>
Have demonstrated teamwork, reliability, and a positive attitude in past roles or projects.</li><li>
Bring strong written and verbal communication skills&mdash;and enjoy presenting your ideas.</li><li>
Are naturally curious with a desire to learn new tools, channels, and strategies.</li>
Thrive in a fast-paced, collaborative environment and enjoy solving problems.<br>
<li>
</li></ul><div><b>What You&rsquo;ll Gain (Benefits)</b><br>
<b>Professional Development</b></div><ul><li>
Hands-on digital marketing agency experience working with real campaigns and real outcomes.</li><li>
One-on-one mentorship from seasoned experts in Paid Media, SEO, or Marketing Automation</li><li>
Opportunities to attend client meetings and strategy sessions.</li><li>
Guidance and feedback designed to accelerate your career path.</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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</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>
The potential base pay range for this role, when annualized, is $26,500.00 - $66,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Digital Marketing Associate - Intern Summer 2026

Join IQVIA and explore 19   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.