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.
Build and administer EDC trials using Veeva CDMS for client projects.
Perform eCRF design, edit check programming, and test data creation.
Manage interface connections and ensure high-integrity database imports.
Celerion is an agile clinical research organization that uses translational medicine to accelerate drug development. The company values integrity, trust, teamwork, and respect and seeks performance-oriented, innovative team players.
Lead customer-facing software implementation projects for global life sciences clients.
Design data solutions and configure Veeva Network MDM to unify customer and product data.
Connect systems, advise stakeholders, and coach junior team members to drive project success.
We are a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue and are a public benefit corporation committed to balancing customer, employee, society, and investor interests.
Be the product evangelist and subject matter expert for Veeva EDC and Veeva DQS, communicating product roadmap directions.
Provide product education to customers in meetings and online communities, ensuring clear communication of value and functionality.
Act as customer advocate, gather and prioritize feedback, and collaborate with product teams to inform release planning.
Veeva Systems is a mission-driven industry cloud pioneer helping life sciences companies accelerate therapy delivery. As a fast-growing public benefit corporation with over $3B in revenue, it values customer and employee success.
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.
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.
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.
Plan, lead, and oversee projects using project management processes to meet deadlines and budgeted costs.
Analyze and research business problems, design innovative solutions, and develop/maintain programs for the clinical data repository.
Collaborate with customers and IT, conduct tests, and provide off-hours support to ensure quality and service.
Capital Blue Cross is a health insurance company and independent licensee of the Blue Cross Blue Shield Association. They provide health insurance plans and services to members in Pennsylvania and are an equal opportunity employer.
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.
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.
Help implement and maintain new features within the Veeva Safety suite.
Work closely with customer business and IT staff to understand and design solutions.
Guide customers in adopting Vault and industry best practices for post-implementation success.
Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies accelerate therapies to patients. As a fast-growing SaaS company surpassing $3B in revenue, it operates as a public benefit corporation balancing customer, employee, society, and investor interests.
Review protocols and support design and configuration of eCOA.
Build, design and consult on eCOA solutions.
Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.
Lead and support statistical programming deliverables for oncology clinical studies.
Ensure high-quality programming with CDISC standards and regulatory compliance.
Collaborate with cross-functional teams including statisticians, data managers, and study leaders.
ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 28 years of experience and over 4,000 professionals in more than 20 countries, with a culture focused on quality, professional development, and supportive collaboration.
Analyze, design and develop cutting-edge software for provider data management on a new product.
Work with a global cross-functional team to build cloud-native, large-scale, scalable data pipelines.
Take full ownership of the software development lifecycle, including planning, design, development, test and deployment.
HealthEdge offers AI-powered operational infrastructure for health insurance companies. With strong market momentum and a growing number of health plans choosing them, they are investing in their people to shape the future of healthcare technology.