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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. At least 7+ years of CRO experience with knowledge of clinical systems, the data points stored within them and data flow paths.

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.

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 all Data Management vendors. Work closely with the DTL to enable data flow for all DM 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 Infosario 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.

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