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IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. With a workforce of approximately 88,000 employees across more than 100 countries, IQVIA leverages advanced analytics, high-quality health data, and Healthcare-grade AI to accelerate the development and commercialization of innovative medical treatments. The company is dedicated to improving patient outcomes and population health through its extensive portfolio of solutions and expertise in healthcare and life sciences.

<div>San Mateo, United States of America | Full time | Home-based | R1529117</div>
<br><div><div>The <b>Solution Sales Specialist</b> develops new business for IQVIA&rsquo;s strategy and analytics portfolio, including <b>Provider Strategy Solution Software (PSS), Market Strategy Solution Software (MSS), Provider Relationship Management software (PRM), Consumer Share of Wallet (CSoW), </b>and <b>custom data analytics.</b></div><div>
This role brings deep product and market expertise to <b>hospital </b>and <b>health system clients</b>, translating complex data assets into actionable insights that support growth, market strategy, service line optimization, and provider engagement.</div><div><b>
Responsibilities:</b></div><ul><li>
Responsible for identifying, qualifying, and advancing revenue opportunities across new and existing accounts in the <b>hospital</b> and <b>health systems industry</b>, through a consultative, insight driven sales approach.</li><li>
Drives growth and revenue for assigned strategy and analytics solutions by partnering with hospital and health system leaders to address strategic, operational, and performance challenges.</li><li>
Serves as a <b>subject‑matter expert</b> for assigned products, maintaining deep knowledge of data sources, analytics methodologies, and real‑world applications within health system enterprises.</li><li>
Partners with Account Executives and broader account teams to shape <b>account strategy, opportunity prioritization, and solution positioning</b> aligned to client objectives.</li><li>
Collaborates with Account Team to target and validate opportunities for assigned customers / territory.</li><li>
Engage stakeholders at all levels, including strategy, finance, marketing, physician relations, and executive leadership.</li><li>
Develops and delivers compelling, insight‑led proposals and presentations that clearly articulate IQVIA&rsquo;s differentiated value that results in winning sales.</li><li>
Coordinates internal resources (product, analytics, consulting, and delivery teams) to design solutions that address client‑specific needs and maximize impact to customers.</li><li>
Maintains ownership through implementation, ensuring successful delivery, adoption, and customer satisfaction.</li><li>
Seeks &ldquo;starburst&rdquo; opportunities within existing customers to grow revenue opportunities across the IQVIA suite of offerings.</li>
As part of the sales process, gather market and client intelligence and provide strategic feedback to Marketing, Consulting, Service, and Sales to strengthen or product offerings and capture additional business.<br>
<li>
</li></ul><div><b>Requirements &amp; Qualifications:</b><br>
</div><ul><li>To be eligible for this position, you must reside in the same country where the job is located.</li><li>
Bachelor's Degree Required.</li><li><b>
US Remote </b>with <b>West Coast territory </b>and <b>ability to travel approximately 25% required.</b></li><li>
5+ years relevant sales or account management experience with hospital and/or health systems industry experience, required.</li><li>
Strong understanding of <b>hospital </b>and <b>health system market dynamics</b>, including service line strategy, referral patterns, market share, and financial performance.</li><li>
Solid knowledge of one or more IQVIA specialty products and the impact that the product can achieve when implemented within a client&rsquo;s business processes.</li><li>
Familiarity with IQVIA core products, account management, and information solutions/consulting services portfolio. Understands how solutions integrate across the enterprise</li><li>
Excellent presentation and writing skills, act with a sense of urgency, and be able to work both independently and within a team environment.</li><li>
Proven ability to influence senior stakeholders, articulate complex concepts clearly, and deliver executive‑ready presentations and written materials.</li><li>
Must have successful experience identifying and closing new business opportunities and developing positive relationships at all levels of client management and within the IQVIA sales, consulting and marketing teams.</li><li>
Track record of identifying, advancing, and closing new business while building trusted client relationships.</li><li>
Key Characteristics: Revenue Driven, knowledgeable, consultative, problem solver, customer focused, strategic, creative, resourceful, fast &amp; flexible, team player, organized, effective negotiator.</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 $73,000.00 - $182,600.00. 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>

Solution Sales Specialist

<div>Houston, United States of America | Full time | Home-based | R1527808</div>
<br><div><div><b>About Cedar Gate Technologies</b></div><div>
Cedar Gate Technologies, an IQVIA business, enables payers, providers, employers, and service administrators to excel at value-based care with a unified technology and services platform delivering analytics, care, and payment technology on a single data management foundation. At Cedar Gate, you&rsquo;ll be part of a collaborative, innovative environment where great ideas thrive. We invest deeply in our people through ongoing training, comprehensive benefits, and a strong culture of teamwork, offering the chance to grow your skills while contributing to high impact initiatives for some of the world's most dynamic companies.</div><div><b>
Position Summary</b></div><div>
As a Senior Client Services Representative - Healthcare Operations at Cedar Gate Technologies, an IQVIA business, you&rsquo;ll be at the heart of our exciting growth journey in Bundle Solutions! You&rsquo;ll create innovative workflows, document essential processes, and turn bundle definitions into powerful system configurations. This hands-on role is perfect for someone eager to dive into healthcare claims workflow analysis while collaborating with software development, implementation, IT, and claims operations teams. Working together, this team ensures a smooth client onboarding experience for all by meticulous testing plans, leading vibrant discussions with new bundle clients, and fostering creativity and teamwork among stakeholders. With your strong analytical and design skills, you&rsquo;ll tackle various value-based care requirements, and the management team will look to you for visionary insights on workflow direction and project implementation. Each of your projects will present unique challenges and exciting opportunities for growth over several weeks to months. Get ready to make a difference in the healthcare industry.</div><div><b>
Roles &amp; Responsibilities</b></div><ul><li>
Inspire the Value-Based Care Operations team by serving as a business leader and process expert, ensuring the successful design, documentation, and configuration of new bundles and their associated claims workflows.</li><li>
Translate process updates and refine strategies to guarantee a smooth transition to claims administration.</li><li>
Create use cases for all testing phases related to new value-based clients.</li><li>
Execute regression testing and user acceptance testing, working with claims staff</li><li>
Lead new initiatives for operating new value-based arrangements by collaborating with Product and Development teams throughout the software development life cycle.</li><li>
Enhance and create claims-related tools to empower operational staff, ensuring efficient and effective usage in their daily tasks.</li></ul><div><b>
Job Location</b></div><div>
United States &ndash; Remote</div><div><b>
Work Arrangement</b></div><div>
U.S. residents only; work must be performed within the United States.</div><div><b>
Experience / Qualifications</b></div><ul><li>
At least 4 years of analysis experience working for a healthcare company is required, with some experience in healthcare claims highly preferred</li><li>
2 or more years of experience with healthcare data transfers required</li><li>
2 years of experience as a business analyst or in similar project-based delivery work is required</li><li>
Strong mathematics and reasoning skills to solve complex problems effectively.</li><li>
Communicate with clarity and confidence, tailoring your message to connect with any audience.</li><li>
Engage in professional discussions to convey information with impact and influence.</li><li>
Analyze the strengths and weaknesses of diverse solutions, making informed and decisive choices.</li><li>
Bachelor&rsquo;s degree in a related field or equivalent work experience.</li><li>
Capitation or Value-Based Care experience is preferred</li><li>
Prior experience using Cedar Gate Technologies software, especially EZ-CAP is preferred</li><li>
To be eligible for this position, you must reside in the same country where the job is located.</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 is 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>

Senior Client Services Representative - Healthcare Ops

<div>Riyadh, Saudi Arabia | Full time | Hybrid | R1522167</div>
<br><div><h3 class="jobSectionHeader"><b>About the Role</b></h3><div>
We are seeking a highly skilled <b>Cloudera Engineer</b> to join our Big Data team. In this role, you will design, build, and manage Hadoop clusters using Cloudera technologies, ensuring optimal performance, scalability, and security. You will collaborate with cross-functional teams to deliver robust big data solutions that power critical business insights.</div><h3 class="jobSectionHeader"><b>
Key Responsibilities</b></h3><ul><li>
Build and configure new clusters and projects involving Cloudera (CDH) technologies.</li><li>
Manage storage, performance tuning, and volume management for Hadoop clusters.</li><li>
Troubleshoot and resolve application and cluster issues, escalating when necessary.</li><li>
Handle cluster design, capacity planning, performance optimization, monitoring, and scaling.</li><li>
Perform standard system administration tasks, including user management, permissions, and upgrades.</li><li>
Monitor and resolve day-to-day cluster issues, ensuring SLA compliance.</li><li>
Support users with administrative needs and optimize job performance.</li><li>
Perform SQL queries and performance tuning across all levels.</li><li>
Collaborate with cross-functional teams to set up production environments and enable business solutions.</li><li>
Develop scripts to automate reporting and maintenance activities.</li><li>
Implement backup and recovery strategies using Cloudera Replication Manager.</li><li>
Address live performance and stability issues and prevent recurrence.</li><li>
Support data engineering efforts, ETL pipelines, and data science teams using Python and Scala.</li></ul><h3 class="jobSectionHeader"><b>
What We&rsquo;re Looking For</b></h3><ul><li>
Proven experience in Hadoop administration and Cloudera (CDH) technologies.</li><li>
Strong knowledge of cluster design, performance tuning, and troubleshooting.</li><li>
Proficiency in SQL and scripting for automation.</li><li>
Familiarity with backup/recovery strategies and operational best practices.</li><li>
Ability to support data engineering and data science teams.</li><li>
Strong problem-solving skills and ability to work under pressure.</li></ul><h3 class="jobSectionHeader"><b>
Why Join Us?</b></h3><ul><li>
Work on cutting-edge big data technologies in a collaborative environment.</li><li>
Opportunity to influence architecture and performance strategies.</li><li>
Be part of a team that values innovation, efficiency, and continuous improvement.</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>

Cloudera Engineer

<div>Carlsbad, United States of America | Full time | Field-based | R1541497</div>
<br><div><div>Job Overview<br>
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.</div><div>
Essential Functions<br>
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.</li><li>Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li><li>Collaborate and liaise with study team members for project execution support as appropriate.</li><li>If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.</li><li>If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.</li></ul></div><div>
Qualifications<br>
<ul><li>Bachelor's Degree Degree in scientific discipline or health care preferred.
</li><li>Requires at least 1 year of on-site monitoring experience.
</li><li>Equivalent combination of education, training and experience may be accepted in lieu of degree.
</li><li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).</li><li>Good therapeutic and protocol knowledge as provided in company training.</li><li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).</li><li>Written and verbal communication skills including good command of English language.</li><li>Organizational and problem-solving skills.</li><li>Effective time and financial management skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li></ul></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 $71,900.00 - $189,000.00. 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>

Clinical Research Associate, Sponsor Dedicated

<div>Overland Park, United States of America | Full time | Field-based | R1541497</div>
<br><div><div>Job Overview<br>
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.</div><div>
Essential Functions<br>
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.</li><li>Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li><li>Collaborate and liaise with study team members for project execution support as appropriate.</li><li>If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.</li><li>If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.</li></ul></div><div>
Qualifications<br>
<ul><li>Bachelor's Degree Degree in scientific discipline or health care preferred.
</li><li>Requires at least 1 year of on-site monitoring experience.
</li><li>Equivalent combination of education, training and experience may be accepted in lieu of degree.
</li><li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).</li><li>Good therapeutic and protocol knowledge as provided in company training.</li><li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).</li><li>Written and verbal communication skills including good command of English language.</li><li>Organizational and problem-solving skills.</li><li>Effective time and financial management skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li></ul></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 $71,900.00 - $189,000.00. 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>Parsippany, United States of America | Full time | Field-based | R1541452</div>
<br><div><div>Job Overview:<br>
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.<br>
</div><div>Essential Functions:<br>
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.</li><li>Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.</li><li>Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li><li>Collaborate and liaise with study team members for project execution support as appropriate.</li><li>If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.</li><li>If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.</li></ul><br>
</div><div>Qualifications:<br>
<ul><li>Bachelor's Degree Degree in scientific discipline or health care preferred. Req</li><li>Requires at least 1.5 years of year of on-site monitoring experience. Req</li><li>Equivalent combination of education, training and experience may be accepted in lieu of degree. Req</li><li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.</li><li>i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li><li>Good therapeutic and protocol knowledge as provided in company training.</li><li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).</li><li>Written and verbal communication skills including good command of English language.</li><li>Organizational and problem-solving skills.</li><li>Effective time and financial management skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li></ul></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 $87,200.00 - $182,000.00. 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>

Clinical Research Associate - Sponsor Dedicated

<div>Durham, United States of America | Full time | Field-based | R1541452</div>
<br><div><div>Job Overview:<br>
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.<br>
</div><div>Essential Functions:<br>
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.</li><li>Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.</li><li>Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li><li>Collaborate and liaise with study team members for project execution support as appropriate.</li><li>If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.</li><li>If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.</li></ul><br>
</div><div>Qualifications:<br>
<ul><li>Bachelor's Degree Degree in scientific discipline or health care preferred. Req</li><li>Requires at least 1.5 years of year of on-site monitoring experience. Req</li><li>Equivalent combination of education, training and experience may be accepted in lieu of degree. Req</li><li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.</li><li>i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li><li>Good therapeutic and protocol knowledge as provided in company training.</li><li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).</li><li>Written and verbal communication skills including good command of English language.</li><li>Organizational and problem-solving skills.</li><li>Effective time and financial management skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li></ul></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 $87,200.00 - $182,000.00. 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>

Join IQVIA and explore 81   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

Solution Sales Specialist

Senior Client Services Representative - Healthcare Ops

Cloudera Engineer

Clinical Research Associate, Sponsor Dedicated

Clinical Research Associate, Sponsor Dedicated

Clinical Research Associate - Sponsor Dedicated

Clinical Research Associate - Sponsor Dedicated