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Clinical Programmer Medidata Rave Jobs (NOW HIRING)

Medidata Solutions

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

The AI features developed will power modern clinical trial study design and study conduct with Rave ... Medidata believes that benefits should connect you to the support you need when it matters most and ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

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

As of Aug 16, 2026, the average hourly pay for clinical programmer medidata rave in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical programmer Medidata Rave?

To succeed as a Clinical Programmer Medidata Rave, you need a strong background in clinical data management, programming (such as SAS or SQL), and knowledge of clinical trial processes, often supported by a degree in life sciences, computer science, or a related field. Expertise in using Medidata Rave EDC, along with familiarity with CDISC standards and relevant certifications, is highly valued. Attention to detail, problem-solving ability, and effective communication are standout soft skills for this role. These competencies ensure accurate data capture, smooth collaboration with study teams, and the integrity of clinical trial results.

What are some common challenges faced by clinical programmers specializing in Medidata Rave, and how can they be addressed?

Clinical Programmers working with Medidata Rave often face challenges such as managing complex protocol requirements, ensuring data quality across large datasets, and adapting to evolving regulatory standards. Addressing these challenges usually involves staying current with system updates, maintaining clear documentation, and collaborating closely with data managers, biostatisticians, and clinical teams to resolve discrepancies efficiently. Effective troubleshooting skills and ongoing training on the Medidata Rave platform can also help streamline workflow. Being proactive in communicating potential issues and actively contributing to process improvements can set you apart and help ensure the success of clinical studies.

What is a clinical programmer Medidata Rave?

A Clinical Programmer specializing in Medidata Rave is responsible for designing, developing, and maintaining electronic data capture (EDC) systems for clinical trials. They configure study databases, create edit checks, and ensure data integrity within the Medidata Rave platform. Additionally, they collaborate with clinical data managers and biostatisticians to streamline data collection and validation processes. Their role is crucial in optimizing clinical trial workflows and ensuring compliance with regulatory standards.

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Clinical Programmer Medidata Rave jobs near you
Infographic showing various Clinical Programmer Medidata Rave job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Senior Manager / Manager, Clinical Data Management

Kodiak Sciences Inc.

Palo Alto, CA

Full-time

Re-posted 18 days ago

Job description

Kodiak Sciences is a biopharmaceutical company committed to researching, developing, and commercializing transformative therapeutics to treat a broad spectrum of retinal diseases. We are focused on bringing new science to the design and manufacture of next-generation retinal medicines to prevent and treat the leading causes of blindness globally. This role is on-site at Kodiak's headquarters in Palo Alto, CA. 
 
We are seeking a dedicated and detail-oriented person to support data management activities for clinical trials. This role will contribute to database development, data quality oversight, and vendor coordination to ensure accurate, compliant, and submission-ready data. The ideal candidate will bring strong hands-on experience and a collaborative mindset, working closely with cross-functional teams to drive successful trial execution and regulatory submissions.
 
Responsibilities
  • Support the design, development, and validation of clinical trial databases and electronic Case Report Forms (eCRFs) at the study level.
  • Oversee data cleaning, query resolution, and delivery of high-quality datasets to support trial milestones and regulatory submissions.
  • Collaborate with external data management vendors to ensure timely and high-quality deliverables; track performance against project timelines and quality standards.
  • Participate in the preparation, review, and validation of submission-ready datasets for regulatory filings (e.g., NDA, BLA, MAA).
  • Ensure compliance with industry standards and regulations (GCP, FDA, EMA) and assist in audit and inspection readiness.
  • Coordinate with internal stakeholders including Clinical Operations, Biostatistics, Regulatory Affairs, and IT to ensure smooth data integration and reporting.
  • Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms).
Education / Qualifications
  • Bachelor’s degree in Life Sciences, Data Science, Computer Science, or a related field.
  • 10+ years of experience in clinical data management within the biotech, pharmaceutical, or CRO industry.
  • Experience managing study-level data management activities and working with external vendors.
  • Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM).
  • Demonstrated experience supporting regulatory submissions is a plus.
  • Strong problem-solving, organizational, and communication skills.

Apply