Associate Consultant - Entry-Level Clinical Data Technology Consulting

Veeva Systems is hiring an Associate Consultant for its Consultant Development Program. The role involves working with customers and internal teams to design, configure, and implement clinical data management software, guiding clinical operations and data management teams through implementation.

Responsibilities

• Designing & tailoring the software: You will lead the configuration of our Vault CDMS platform to fit each customer's unique clinical trial requirements—setting up study workflows, structuring clinical data models, and aligning system capabilities to study protocols
• Conducting discovery workshops: You will lead interactive discovery workshops with customer stakeholders (e.g., Clinical Data Managers, CRCs, CRAs) to gather business requirements, map out existing data management workflows, and translate their vision into actionable technical specifications
• .Managing project scope & execution: You will take ownership of core implementation deliverables by scoping study requirements, building timeline estimates, and keeping project milestones on track from study design through go-live
• Guiding the customer as an expert: You will lead the customer with best practices to ensure their clinical data collection and study management processes are optimized for maximum long-term value

Preferred

• A Bachelor's or Master's degree in a quantitative or life science field is preferred, such as:
• Biomedical Engineering, Health Informatics, Bioinformatics, Biostatistics, Data Science, Computer Science, Engineering
• Clinical Research, Public Health, Biology, Pharmacology
• Prior experience (internships, co-ops, academic projects, or entry-level roles) in one or more of the following areas is highly valued:
• Data entry or management in a healthcare/research setting, or experience at a CRO, as a Clinical Research Associate (CRA), or Clinical Research Coordinator (CRC)
• Clinical trial operations, monitoring, or clinical data management
• Data analysis using statistical software (SAS, SPSS, Python, R)
• Design training, UX Design, or Human Factors Studies
• Business or technical consulting
• Speech and Debate or Manufacturing
• Biomedical Engineering
• Health Informatics
• Bioinformatics
• Biostatistics
• Data Science
• Computer Science
• Clinical Research
• Public Health
• Biology
• Pharmacology
• Healthcare Data Entry
• Healthcare Data Management
• Research Data Management
• CRO Experience
• Clinical Research Associate Experience
• Clinical Research Coordinator Experience
• Clinical Trial Operations
• Clinical Trial Monitoring
• Clinical Data Management
• Statistical Analysis
• SAS
• SPSS
• Design Training
• UX Design
• Human Factors Studies
• Business Consulting
• Technical Consulting
• Manufacturing
• Public Speaking
• Debate

Benefits

• Medical, dental, vision, and basic life insurance
• Flexible PTO and company paid holidays
• Retirement programs
• 1% charitable giving program
• Perform well, and in one year you’ll receive a compensation increase
• Perform well, and in one year you’ll participate in our bonus program
• Long-term, our Work Anywhere policy allows you flexibility to work from the office or from your home.

Company

• Life sciences industry cloud software, AI, data, and consulting
• Pleasanton, California, USA
• http://www.veeva.com/
• Founded in 2007
• 5001-10000 employees

Qualifications

• Basic familiarity with database concepts. For example, SQL for querying relational databases and Python or R for data manipulation and analysis
• You thrive in a challenging, intense environment that rewards initiative and rapid learning
• You have a genuine desire to be hands-on with software and master new technologies
• You are fluent in English with excellent verbal and written communication skills
• You are a strong critical thinker with a proven track record of analytical performance
• Veeva is a Public Benefit Corporation (PBC) and a “do the right thing” company, and we expect that from all employees
• A commitment to excellence and passion for working hard to achieve results
• Open to recent graduates of Bachelor's or Master's programs (up to 2 years postgraduate experience maximum)
• Qualified candidates must be legally authorized to be employed in the United States. Veeva does not provide sponsorship for employment visa status (e.g., H-1B, OPT, or TN status) for this employment position
• A Bachelor's or Master's degree in a quantitative or life science field is preferred, such as:
• Biomedical Engineering, Health Informatics, Bioinformatics, Biostatistics, Data Science, Computer Science, Engineering
• Clinical Research, Public Health, Biology, Pharmacology
• Prior experience (internships, co-ops, academic projects, or entry-level roles) in one or more of the following areas is highly valued:
• Data entry or management in a healthcare/research setting, or experience at a CRO, as a Clinical Research Associate (CRA), or Clinical Research Coordinator (CRC)
• Clinical trial operations, monitoring, or clinical data management
• Data analysis using statistical software (SAS, SPSS, Python, R)
• Design training, UX Design, or Human Factors Studies
• Business or technical consulting
• Speech and Debate or Manufacturing

Required skills

• Business and Technical Consulting, Clinical Data Management, Clinical Research, Clinical Trial Operations, Healthcare Data Management, Human Factors Studies, Python, R, SAS, SPSS, SQL, UX Design

Preferred skills

• Business or technical consulting, Clinical Research, Public Health, Biology, Pharmacology, Design training, UX Design, or Human Factors Studies, Speech and Debate or Manufacturing

Experience

• Entry level