Act as a trusted advisor configuring Veeva Vault CDMS for clinical trial data management.
Develop SQL-based custom listings and support data integrations and user acceptance testing.
Collaborate with customers, CROs, and vendors on study design and go-live activities.
Veeva Systems is a mission-driven cloud software company helping life sciences firms bring therapies to patients faster. As a fast-growing public benefit corporation with over $3B in revenue, it values customer success, employee success, and speed while supporting flexible work anywhere.
Act as a trusted advisor to customers and clinical sites, ensuring trial designs meet goals and providing training.
Lead database development activities, configure forms and rules in Vault CDMS, and build custom SQL listings.
Support requirements gathering, user acceptance testing, and risk management to keep projects compliant.
Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies, it surpassed $3B in revenue and is a public benefit corporation committed to balancing stakeholder interests.
Provide expert technical support and leadership in clinical trial reporting using advanced SAS features.
Perform quality control checks and ensure accuracy and consistency of SAS code and output.
Collaborate with cross-functional teams to support electronic submissions and compliance with regulatory standards.
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. With over 30 years of history, the company is consistently recognized as one of the industry's top places to work, including 14 consecutive years on Science magazine's Top Employers list and one of Fortune’s 100 Best Companies to Work For.
Lead data management activities for clinical and epidemiologic research studies from start-up through closeout.
Perform advanced SAS programming to clean, validate, and manage complex research datasets.
Design and maintain study databases, validation rules, and data quality procedures.
DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering, and digital transformation. The company employs experts in public health and health operations and is committed to innovation and improving lives.
Lead the development and execution of statistical analysis plans for large-scale real-world evidence studies.
Work directly with cross-functional teams and senior stakeholders to design data-driven solutions for a high-profile sponsor.
Oversee and mentor junior analysts, driving best practices and innovative analytics workflows.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, the company emphasizes a supportive culture, continuous training, and below-industry-average turnover rates.
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
Create datasets, tables, listings, and figures according to study requirements and CDISC standards.
Collaborate with Biostatistics, Data Management, and Clinical teams to ensure quality and timelines.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of experience and 4,000+ professionals across more than 20 countries, we foster a supportive culture with below-industry-average turnover.
Design, develop, and enhance applications on the SAS Viya Cloud Platform with advanced SAS programming and Python API integrations.
Support production analytics capabilities, ETL processes, and data pipelines while troubleshooting incidents and performance issues.
Create and maintain technical documentation, provide code reviews, and participate in solution design and release planning.
NTT DATA is a Top 5 global IT services provider with over 190,000 professionals across 50+ countries. They combine industry expertise with consulting, technology, AI, cloud, and infrastructure to help organizations innovate and transform.
Develop and quality-control SDTM datasets supporting clinical research and regulatory submissions.
Program complex SDTM datasets and trial design domains using SAS.
Collaborate with sponsors, data operations, and cross-functional teams to ensure timely project delivery.
This partner company is a clinical research organization that develops SDTM datasets for regulatory submissions. The environment is collaborative, fast-paced, and focused on quality and operational excellence.
Manage all programming aspects of clinical databases from study start to post-lock, ensuring compliance with regulatory guidelines.
Lead operational study teams and provide technical training to end users and junior staff.
Communicate project status to internal teams and clients, and perform project forecasting and budget management.
Precision for Medicine is a life sciences company that provides clinical research services, including database programming and data management. The company is growing and seeks a Principal Database Programmer to join its European team, fostering a collaborative and dynamic work environment.
Lead full-lifecycle clinical data management across all trials, ensuring data quality and integrity from eCRF builds to database locks and submission readiness.
Build and scale a high-performing Data Management organization, driving talent development and operational excellence.
Ensure strict compliance with global regulatory standards and manage CRO relationships to deliver high-quality results.
Kailera Therapeutics is a biotechnology company developing novel therapies for obesity and related conditions. The company fosters an entrepreneurial, team-oriented culture and is committed to creating an inclusive workplace.
Lead technical sales engagements with healthcare and life sciences clients, gathering requirements and demonstrating SLC capabilities.
Conduct proof-of-concept activities and provide architectural guidance for deploying SLC in existing IT ecosystems.
Act as a subject matter expert in SAS language and statistical programming, authoring industry-specific presentations and workshops.
Siemens Software is a leading industrial software company that builds technology to shape the real world. With 30,000 employees across more than 200 countries, we foster a culture of trust, autonomy, and inclusion.