IQVIA

Mgr, Database Management Systems

IQVIA • $84K — $211K *
New York, NY 10025In-Person
Healthcare
Less than 5 years of experience
Today
Be an Early Applicant
Job Overview by Ladders

Qualifications

  • Strong clinical domain knowledge with understanding of clinical trial phases.
  • Prior experience in clinical research, pharmaceutical, biotechnology, healthcare, or CRO industry.
  • Hands-on experience with SAS programming for Edit Check Listings and Data Imports.
  • Proficiency in SAS Output Delivery System (ODS) for generating reports in multiple formats.
  • Experience in reading raw data files and managing clinical datasets.

Responsibilities

  • Lead development of global clinical data standards compliant with CDISC.
  • Build and maintain eCRFs and associated components in Medidata Rave.
  • Create SAS programs for data validation and reporting.
  • Manage clinical datasets using Advanced SAS and Macros.
  • Collaborate with various teams to ensure standard implementation in data management.
  • Drive process improvements and support governance committees.
  • Mentor junior team members to enhance skillsets.

Benefits

  • Comprehensive health and welfare programs.
  • Incentive plans and bonuses available.
  • Opportunities for professional development and advancement.
Full Job Description

Manager, Database Management Systems

Job Summary
Seeking an experienced clinical data professional to lead database management and clinical data standards activities supporting global clinical trials. This role will serve as a subject matter expert in clinical data standards, Medidata Rave global library development, and SAS programming, partnering with cross-functional teams to ensure high-quality, standardized clinical data collection and reporting.

Key Responsibilities

  • Lead development and maintenance of global clinical data standards, including CDISC-compliant operational data mappings and SDTM standards.
  • Build and maintain Medidata Rave global library objects, including eCRFs, edit checks, and CRF Completion Guidelines.
  • Develop SAS programs for edit checks, data imports, listings, custom reports, and clinical data validation.
  • Create and manage clinical datasets from raw data using Base SAS, Advanced SAS, Macros, PROC SQL, and SAS ODS.
  • Support CRF design, annotated CRFs, data mapping specifications, and define.xml requirements.
  • Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CRO partners to ensure consistent standards implementation.
  • Drive process improvements, support governance committees, and provide mentorship to junior team members.
  • Ensure compliance with CDISC standards, GCP, ICH guidelines, and regulatory requirements.

Required Qualifications
  • Strong clinical domain knowledge with a solid understanding of clinical trial phases.
  • Prior work experience must be within the clinical research, pharmaceutical, biotechnology, healthcare, or CRO industry.
  • Hands-on experience programming Edit Check Listings using SAS.
  • Experience with Data Import Programming using SAS.
  • Experience utilizing SAS Output Delivery System (ODS) to generate reports in RTF, PDF, and HTML formats.
  • Experience reading raw data files, creating data structures, handling missing values, troubleshooting programming errors, and managing clinical data.
  • Experience appending and concatenating SAS datasets.
  • Proficiency developing reports using PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, and PROC SQL.
  • Strong programming experience with SAS Macros and SQL.
  • Experience creating SAS datasets from raw clinical data, including status and efficacy datasets.
  • Ability to develop project-specific macros and formats, load client data from external platforms, and prepare datasets for client delivery.
  • Experience creating clinical listings and custom reports based on business requirements.
  • Knowledge of Vendor Import Programming.
  • Strong technical expertise in Base SAS, Advanced SAS, SAS Macros, SAS SQL, and SAS Grid.
  • Ability to develop code using Base SAS programs, SAS procedures, and standardized macros.
  • Excellent written and verbal communication skills.

Preferred Qualifications

  • Experience with CDASH and ADaM standards.
  • Extensive Medidata Rave global library development experience.
  • Knowledge of MedDRA, WHODrug, annotated CRFs, and data mapping specifications.
  • Experience with Veeva, Medrio, Oracle Clinical, TrialGrid, or similar EDC systems.
  • Demonstrated ability to lead cross-functional initiatives in a global clinical development environment.

The potential base pay range for this role, when annualized, is $84,600.00 - $211,600.00. 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.

About IQVIA

Innovex offers superior and creative advice to corporations. In addition, they raised venture capital for our own affiliate companies, in addition to having assisted clients in fund-raising efforts, new venture outreaches, and financing. Their engineers and technical staff offer varied backgrounds in manufacturing, high tech, product design, quality control, safety, biomechanics, and robotics.

IQVIA Careers

Join the vibrant team at IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services to the healthcare industry. IQVIA is recognized for its commitment to innovation, leadership in healthcare, and a culture that celebrates diversity and inclusion.

Work You’ll Do

At IQVIA, we offer job opportunities that empower you to leverage your skills and drive healthcare forward. Become part of a team that thrives on innovation and the pursuit of operational excellence, helping to improve patient outcomes across the globe.

Transform Your Career

IQVIA is the place where you can transform the world of healthcare while advancing your career. With a variety of positions available, from research and development to business analytics, IQVIA is at the forefront of the industry. Our leadership is committed to fostering a culture of growth and professional development, making IQVIA a prime environment for both seasoned professionals and those seeking an internship to kickstart their career.

Innovative Work Environment

Join over 50,000 dedicated professionals in a dynamic environment where technology meets healthcare. At IQVIA, innovation isn’t just a buzzword; it's the backbone of how we solve complex challenges. With cutting-edge resources and a collaborative global team, your work at IQVIA directly contributes to advancements in life sciences.

Career Development and Benefits

IQVIA believes in nurturing its team members not just as employees but as individuals seeking to grow their careers. We support this with unmatched benefits, diversity training, and opportunities for leadership development. Our commitment to your career growth is matched by our dedication to providing a supportive and inclusive workplace.

Explore Job Opportunities

Whether you’re looking for a full-time position, part-time work, or a graduate internship, IQVIA offers a range of employment options to match your career ambitions. Our hiring process is designed to be transparent and engaging, helping you to understand where your skills can best be utilized within the company.

Networking and Professional Development

At IQVIA, networking and professional development are part of our DNA. Engage with industry leaders, participate in global conferences, and take advantage of our in-house training programs designed to enhance your skills and advance your career.

Stay Connected

Join Our Team Search open positions that match your skills and interests. We look for passionate, curious, creative, and solution-driven team players. Explore the diverse job opportunities at IQVIA and find where you can make an impact.

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Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. Discover the exciting and rewarding career opportunities that await at IQVIA. Embark on a journey of growth, innovation, and leadership at IQVIA. Shape your future in an environment that values diversity and fosters professional development. Join IQVIA today and transform healthcare through the power of information and technology.
Learn more about IQVIA
Size
82,000 employees
Market Cap
$37.5 billion
Industry
Pharmaceuticals & Biotech
Net Income
$279 million
Founded
2016
5 Year Trend
+15.3%
Revenue
$11.3 billion
NASDAQ
IQV
* Ladders Estimates

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