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Internship Medidata Rave Programmer Jobs (NOW HIRING)

... Medidata Rave and or other (Veeva EDC or Oracle EDC or other smaller systems) and clinical trial ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

$164 - $221/hr

... Medidata Rave and or other (Veeva EDC or Oracle EDC or other smaller systems) and clinical trial ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

... Medidata Rave and or other (Veeva EDC or Oracle EDC or other smaller systems) and clinical trial ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

Data Architect

Austin, TX · On-site

$100 - $130/hr

Proficiency with at least two major EDC platforms (e.g., Medidata Rave, Veeva Vault CDMS, Oracle ... Collaboration with engineering teams in Lahore and QC operations in Dubai * Conference and ...

... Medidata Rave and or other (Veeva EDC or Oracle EDC or other smaller systems) and clinical trial ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

Senior Data Scientist

Manhattan, NY · On-site

$114.75 - $153/hr

About the Team Medidata AI organization is building innovative AI products based on the largest ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

$122 - $203/hr

... by Clinical Programming and Biostatistics. Key Responsibilities: • Lead the development ... Medidata Rave, Veeva) to ensure adherence to global collection standards. • Lead standards kick ...

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

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Internship Medidata Rave Programmer information

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How much do internship medidata rave programmer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for internship medidata rave programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What does an internship Medidata Rave programmer do?

An Internship Medidata Rave Programmer assists in designing, developing, and maintaining electronic data capture (EDC) systems using Medidata Rave for clinical trials. Their main tasks include programming study databases, building case report forms (CRFs), and ensuring data quality and compliance with regulatory standards. Interns typically work under the supervision of experienced programmers and may also help troubleshoot technical issues, support data validation, and learn about clinical data management processes. This role provides hands-on experience with clinical trial technology and helps interns build foundational skills for a future career in clinical data programming.

What are the key skills and qualifications needed to thrive as an internship Medidata Rave programmer?

To thrive as an Internship Medidata Rave Programmer, you need a solid background in computer science or life sciences, familiarity with clinical data management concepts, and basic programming skills. Experience with Medidata Rave EDC platform, clinical trial management systems, and understanding of CDISC standards or certifications like Medidata Rave certification are valuable. Attention to detail, problem-solving abilities, and strong communication skills help you collaborate effectively with clinical teams and ensure data integrity. These skills are essential for supporting efficient, compliant data capture and management in clinical research environments.

What are some typical projects or tasks an internship Medidata Rave programmer might work on?

As an Internship Medidata Rave Programmer, you can expect to assist with building and maintaining electronic case report forms (eCRFs), validating study configurations, and supporting data management teams in clinical trials. You may also help troubleshoot and resolve issues within Medidata Rave, perform quality checks, and contribute to documentation. Collaboration with experienced programmers and data managers is common, providing valuable exposure to real-world clinical data workflows and industry best practices.

What is the difference between Internship Medidata Rave Programmer vs Clinical Data Coordinator?

AspectInternship Medidata Rave ProgrammerClinical Data Coordinator
Required CredentialsBasic knowledge of Medidata Rave, relevant coursework or certificationsDegree in life sciences, healthcare, or related field; often additional certifications
Work EnvironmentInternship setting, often in pharmaceutical or biotech companiesClinical trial sites or sponsor organizations, managing data entry and quality
Industry UsageUsed primarily in clinical data management and EDC system setupUsed in clinical trial data collection, management, and compliance

The Internship Medidata Rave Programmer typically focuses on learning and supporting EDC system setup and data management using Medidata Rave, often as part of an internship program. In contrast, a Clinical Data Coordinator manages data collection, quality control, and compliance during clinical trials. Both roles are essential in clinical research but differ in responsibilities and experience levels.

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Infographic showing various Internship Medidata Rave Programmer job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Senior Manager, Data Engineer, Clinical Operations

Scorpion Therapeutics

Princeton, NJ • On-site

$154 - $186/hr

Other

Medical, Life, Retirement

Posted 8 days ago


Job description

Position Summary

As a Senior Manager, Data Engineer, you will support the Data Engineering community to deliver data and analytics platforms for Global Drug Development (GDD) — Patient & Site engagement and Feasibility & Forecasting.

Key Responsibilities
  • Support cross-functional AI and Data initiatives for Clinical Trial Operations product lines.
  • Develop and enhance data solutions to accelerate clinical R&D data usage (robustness, interoperability, scalability).
  • Collaborate with BI&T, business/data analysts, data engineers, and domain experts to drive adoption of the Data Platform.
  • Deliver solutions for data product development: standardization, testing, lineage, latency requirements, and access governance.
  • Optimize platform performance, scalability, interoperability, availability, and cost using cloud-native parallel processing, Databricks Delta Lake, caching, and partitioning.
  • Use Databricks Unity Catalog for governance, metadata management, and end-to-end lineage.
  • Build self-service data discovery (findability, accessibility, reusability).
  • Maintain documentation; provide technical recommendations.
  • Build/deploy GenAI and NLP applications to improve efficiency, accelerate timelines, mitigate risk, and automate compliance.
  • Operationalize cloud-based GenAI/LLM applications using RAG, fine-tuning, and vector embeddings.
  • Stay current on GenAI/RAG/semantic search/Databricks/cloud orchestration/containerization.
  • Mentor junior analysts/interns/vendor resources.
Qualifications & Experience
  • 7+ years in Data Engineering/Analytics/AI-ML with hands-on cloud data capabilities.
  • Strong communication and stakeholder management; ability to influence adoption.
  • Databricks expertise (Delta Lake, Unity Catalog, Workflows, Mosaic AI, MLflow) and certification strong plus.
  • Cloud-native data platforms; ETL/ELT, data modeling, semantic analytics; DevOps experience.
  • Python, SQL, Spark (PySpark on Databricks), GenAI frameworks; LLM architectures, RAG, prompt engineering, agentic frameworks.
  • Production-grade GenAI apps, predictive models, self-service analytics.
  • Working knowledge of LLM/GenAI approaches (RAG, fine-tuning, vectorization, agentic frameworks, prompt engineering).
  • Life sciences/clinical trial operations knowledge strongly preferred; familiarity with Veeva Vault, Medidata Rave, IRT preferred.
Benefits (as stated)
  • Health Coverage; Wellbeing support; Financial wellbeing/protection (401(k), disability, life insurance, etc.).
Compensation Overview (as stated)
  • Princeton, NJ: $153,770–$186,327 (full-time). Additional incentives may apply based on eligibility.
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