This position is Full-Time and remote based anywhere in North America

Why DSSS?

Data Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work within an eco-system where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies. With IQVIA's DSSS business unit, you are not just another cog in the machine; you become a core part of a dynamic team dedicated to reshaping the future of healthcare.

Additional Benefits:

• Home-based remote work opportunities
• Great work/life balance
• Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors
• Cohesive team environment fostering a collaborative approach to study work
• Variety of therapeutic areas, indications and, study phases
• Job stability; long-term engagements and development opportunities
• Technical training and tailored development curriculum
• Career advancement opportunities

Job Requirements:

• Independently develop accurate and CDISC compliant SDTM and ADaM specifications for Phase 1/early phase studies
• Independently develop/validate programs that generate analysis datasets based on ADaM specifications.
• Independently develop/validate programs that generate tables and listings specified in the protocol or the Statistical Analysis Plan (SAP).
• Good understanding of regulatory requirements. Prepare XPTs, Define.xml, Reviewer’s Guide, and analysis metadata report, executable programs for CRT packages.
• Run P21 checks and resolve the P21 validation report related error and document details.
• Perform quality control on final reports. Generate the ad hoc and custom reports as requested.
• Provide QC and validation reports and document corresponding details.
• Communicate with programming and statistics leads, data managers, and other team members.
• Provide project progress updates of programming activities

Education/Experience:

• Minimum bachelor’s degree in Statistics, Computer Sciences, Bioinformatics, or related field PLUS 6+ years of hands-on clinical trials industry experience.
• Recent, in-depth experience supporting early phase/Phase 1 studies within oncology TA required
• Prior experience working in GPS sponsor system strongly preferred

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

The potential base pay range for this role, when annualized, is $106,200.00 - $177,000.00. 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.