Clinical Data Strategist

IQVIA; Durham (NC); On-site; USD 87,000 - 216,000; Full time

Job summary

IQVIA LLC in Durham, North Carolina is seeking a Clinical Data Strategist responsible for setting up systems (EDC, IRT) and ensuring data standards for seamless integration with the Data Factory and CDR.

You will guide data flow patterns across multiple systems, lead vendor data set-up, and develop the Systems Integration Plan to minimize latency and enable real-time analytics. The role requires CRO experience and strong communication skills to work with global IT and study teams.

Qualifications

• Experience in Drug Discovery or clinical trial data management.
• Strong critical thinking and analytical skills with attention to detail.
• Excellent written, interpersonal, and verbal communication.
• Ability to influence, resolve problems, and lead discussions.
• Knowledge of data integration, standards, and governance.

Responsibilities

• Guide data flow design patterns across multiple systems to enable real-time analytics.
• Lead vendor data set-up for Data Management and other functions.
• Develop and manage the Systems Integration Plan with risk analysis.
• Collaborate with global IT to resolve data integration issues and ensure quality.
• Educate teams on SOPs and data standards during RFI and post-award phases.

Skills

Data integration

Leadership

Analytical thinking

Project management

Communication

Education

Bachelor in Science/Computer Science/Information Technology

Tools

EDC

IVxS

Data Factory

CTMS

QRPM

CDOS

SLDRs

Job description

## Clinical Data StrategistApply: Durham, North Carolina, United States of America: Full time: Posted Today: R1553527**JOB OVERVIEW** Performs and oversees the set-up of individual systems (EDC, IRT etc), ensuring data standards are followed leading to successful data integration with the Data Factory (DF)/Clinical Data Repository (CDR). Ensure the data collected and integrated into the Data Factory (DF)/Clinical Data Repository (CDR), can be successfully utilized in all downstream systems by First Patient In (FPI). **RESPONSIBILITIES** • Work directly with project teams to guide/convey optimal data flow design patterns across the enterprise consisting of multiple systems with the end goal to ensure data integrations enable real time Alerts and Analytics • Lead vendor data set-up for Data Management vendors and other functions as required, enabling the data flow for downstream activities (data cleaning, etc). • Complete and manage the 'Systems Integration Plan' to detail the data flow and highlight potential risks/challenges while collaborating with various groups (i.e. IPA, Study Team, CDAT) to provide data standardization and alignment of site visits across systems”. • Champion people, process and technology improvements and standards to enhance quality, increase productivity (internal and external with Investigator sites) and reduce data latency within Quintiles clinical trial systems inclusive of IVxS, EDC, CTMS, QRPM, Data Factory, Triggers and Alerts, Visualizations such as Clinical Analytics and Federated reports, CDOS and SLDRs. • Guide and present study teams with best case options given limitations (e.g. contract, cost, timelines, etc.) with the ability to articulate pros and cons of each approach. • Identify and implement innovative solutions to challenges and influence future decision-making in order to reduce workarounds. • Review data transfers specifications to ensure they meet the standards required to develop quality data integrations. • Proactively provide education and training to ensure adherence of the relevant startup SOPs and best practices during the RFI and post-award phases. • Collaborate with the global IT organization as needed to resolve support issues related to data integration or data quality. • Ability holistically understands the process and structure of 5-10 individual systems and determine how the design of one system may impact the ability of another system to function optimally. **REQUIRED KNOWLEDGE, SKILLS AND ABILITIES** Experience working in Drug Discovery, clinical trial conduct, clinical data management or related industries. Excellent critical thinking and analytical skills, strong attention to detail Effective written, interpersonal, and verbal communication skills Strong influencing, problem resolution, motivation, and negotiation skills Solution-oriented approach to challenges Sound leadership and customer service skills Competent presentation skills meeting the needs of all levels Ability to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive management Ability to lead effective meetings Strong organizational and time management skills Ability to manage multiple dependencies across multiple systems to reach a final deliverable Ability to establish and maintain effective working relationships with teams involved in study start up **MINIMUM EXPERIENCE** Bachelor in Science/Computer Science/Information Technology or Bachelor in Technology with 8 to 10 years experience OR equivalent combination of education and experience. 7+ years of CRO experience with knowledge of clinical systems, the data points stored within them and data flow paths.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.comIQVIA 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/eoeIQVIA 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.The potential base pay range for this role, when annualized, is $86,500.00 - $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.