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Internship Medidata Rave Programmer Jobs (NOW HIRING)

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

... Programmer . You will be responsible for administration of EDC Database including evaluation ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

... Programmer . You will be responsible for administration of EDC Database including evaluation ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

The SDTM (Study Data Tabulation Model) Specialist is part of the ACTG and IMPAACT Medidata Rave ... Work directly with the statistician and programmer who is responsible for the ADaM datasets Reports ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

... internship or co-op experience in a clinical or pharma setting will be considered. * Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

... internship or co-op experience in a clinical or pharma setting will be considered. * Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming ...

Senior Clinical Data Manager

Cambridge, MA ยท On-site

$144K - $167K/yr

Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies * Lead ... Expertise with EDC systems, such as Medidata Rave, InForm, Medrio * Excellent organizational and ...

... Medidata Product and Engineering teams. * Change Management: Guide clinical trial sites and ... products beyond Rave or CTMS. * Audit & Compliance Readiness: Ability to maintain meticulous ...

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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 Jun 29, 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 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.

What are the key skills and qualifications needed to thrive as an Internship Medidata Rave Programmer, and why are they important?

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.
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Infographic showing various Internship Medidata Rave Programmer job openings in the United States as of June 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.

LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite day 1

TestingXperts Inc. DBA Damcosoft

San Francisco, CA โ€ข On-site

$109K - $140K/yr

Contractor

Posted 13 days ago


Job description

LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite

Pharma R&D Functional Expert

Location: San Francisco, CA โ€“ Onsite
Type: Contract

We are looking to engage an experienced Pharma R&D Functional Expert for one of our clients in San Francisco.

Role Overview:
The consultant will serve as the primary contact for the development of a data and analytics platform on Databricks, acting as the bridge between customerโ€™s R&D stakeholders and the technical data engineering team. The key responsibility will be to define business rules/logic and provide clear documentation for implementation.

Key Requirements:

  • 8โ€“10 years of experience in the pharmaceutical/biotech industry, specifically in R&D, clinical operations, or bioinformatics data management.
  • Strong communication skills to translate scientific/clinical requirements into technical specifications.
  • Experience with clinical data systems (Medidata RAVE or other EDC platforms).
  • Familiarity with CDISC standards (SDTM, ADaM) and LIMS.
  • Good understanding of clinical trial processes.

Nice to Have:

  • Exposure to genomics data (NGS, gnomAD, GWAS) and bioinformatics data lifecycle.
  • Knowledge of SAS and R in statistical/clinical reporting and regulatory submissions.
  • Experience with data platforms (data lakes, data mesh), cloud (Azure preferred), and Databricks/Spark.
  • Translational medicine experience.

Thanks and Regards,

Rajiv Kumar

Associate Manager

Corporate Office:ย  650 Wilson Lane, Suite 201, Mechanicsburg, PA 17055

Testingxperts Inc DBA Damcosoft

P: +1 631-759-8044ย  Ext 518

E:ย Rajiv.kumar@damcosoft.comย ย 

https://www.linkedin.com/in/rajiv-kumar-38396310a/