We strive every day to create and maintain an environment of inclusion where creativity and new ideas thrive &ndash; where people of all backgrounds work together, trust and learn from each other, and leverage a wide range of thoughts, experience and skills to make a difference. As an essential element of our inclusive, innovative workplace, we continually seek to hire and develop the best employees with a variety of skills and experiences. At IQVIA, across all of our business areas, functions, and geographies, we welcome our employees to bring their authentic selves to work every day. Learn more about our diversity and inclusion efforts at <a href="https://jobs.iqvia.com/diversity">https://jobs.iqvia.com/diversity</a>
Employee Resource Groups
Our commitment to diversity and inclusion is further reflected in our Respectful Workplace Policy and Employee Resource Group (ERG) program. Our ERGs support IQVIA&rsquo;s values and goals and foster the diverse thinking required for innovation. Each of our seven ERGs are entirely employee-led, voluntary and open to all employees.
Women Inspired Network (WIN)
WIN fosters a corporate culture that inspires women to excel in their careers at IQVIA and within the biopharma industry. Learn more at <a href="https://jobs.iqvia.com/diversity">https://jobs.iqvia.com/women</a>
WIN strives to:
<ul style="text-align: justify;">
<li>Promote gender equality, diversity and inclusion to help drive healthcare forward</li>
<li>Enhance professional and personal growth to support female advancement in the healthcare industry</li>
<li>Cultivate mentorship and self-development programs</li>
<li>Build female empowerment and engagement</li>
<li>Facilitate innovative conversation</li>
</ul>
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IQVIA

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PURPOSEProvide expert skills as part of a Medical Data Review team to provide efficient, quality Medical Data Review products that meet customer needs.RESPONSIBILITIES<ul style="text-align: justify;"><li>Serve as a Subject level Data reviewer (SLDR) and Identify any anomalies in patient reported data by performing Subject</li><li>Level Data Review that require further investigation with the clinical site to determine overall accuracy</li><li>Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)</li><li>Provide project management to the team in the area of Project Management and viewed as an expert in data management.</li><li>Drive the delivery of end-to-end study data quality and integrity.</li><li>Provide medical, clinical, and scientific advisory expertise.</li><li>May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings.</li><li>Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. .</li><li>Define data capture requirements in line with protocol and reporting needs.</li><li>Maintain strong customer relationships</li><li>With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions</li><li>Ensure timely follow-up and resolution of compliance issues</li><li>Serve as Subject Matter Expert (SME)</li><li>Serve as POC/ Back-up POC</li><li>Continuously look for opportunities to improve efficiency of tasks and quality of deliverables  Provide therapeutic area/indication training for the project clinical team.</li><li>Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.</li></ul>REQUIRED KNOWLEDGE, SKILLS AND ABILITIES<ul style="text-align: justify;"><li>Good understanding of clinical/medical data.</li><li>Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.</li><li>Proven expertise in the proactive identification of issues.</li><li>Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics.</li><li>Proven ability to work within a matrix team environment requiring minimum level of supervision</li><li>Attention to detail Interpersonal and analytical skills,</li><li>Must have Medical but also an operational focus towards metrics and status information to take the appropriate actions to resolve.</li><li>Excellent communication, interpersonal, customer service, and teamwork skills.</li><li>Excellent organizational and problem-solving skills.</li><li>Excellent project management skills and coaching skills.</li><li>Ability to work with minimal supervision, using available resources,</li><li>Ability to work on multiple projects and manage competing priorities</li><li>Strong customer focus skills</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients</li></ul>MINIMUM REQUIRED EDUCATION AND EXPERIENCE<ul style="text-align: justify;"><li>Medic with 5 year college degree or MBBS; or MD or related field of qualification, with 5 years of relevant work experience; or equivalent combination of education, training and experience</li><li>Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience</li></ul>PHYSICAL REQUIREMENTS<ul><li style="text-align: justify;">Extensive use of telephone and face-to-face communication requiring accurate perception of speech.</li><li style="text-align: justify;">Extensive use of keyboard requiring repetitive motion of fingers.</li><li style="text-align: justify;">Regular sitting for extended periods of time.</li></ul>

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