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Contract Medidata Rave Programmer Jobs (NOW HIRING)

Cape Fox SS

Research Database Developer

Cincinnati, OH · Remote

$90K - $120K/yr

... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ... This position is contingent upon contract award. The salary range (or hiring range) for this exempt ...

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115.86K - $150.79K/yr

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Strong hands-on experience with at least one major EDC platform (Medidata Rave preferred). * Solid ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

... Medidata Rave). * Excellent understanding of data administration and management functions (collection, analysis, data review process, etc.). * Excellent hands on experience on SAS or R programming ...

Vor Bio

Senior Data Manager

Boston, MA

... programming. Suggest design for standard and non-standard data collection, identify any gaps in ... Must have Medidata RAVE experience. * Strong project management; exhibits expertise in metrics ...

Kite Pharma

OR

Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics ... Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ...

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

As of May 28, 2026, the average hourly pay for contract 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 are the key skills and qualifications needed to thrive as a Contract Medidata Rave Programmer, and why are they important?

To thrive as a Contract Medidata Rave Programmer, you need expertise in clinical data management, EDC systems, and programming languages such as SQL or SAS, typically backed by a degree in life sciences or computer science. Proficiency with Medidata Rave, eCRF design, and understanding of CDISC standards are essential, along with relevant certifications like Medidata Rave Certified Professional. Attention to detail, analytical thinking, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills and qualifications are vital for building reliable clinical databases and supporting accurate data capture in regulated clinical trials.

How does a Contract Medidata Rave Programmer typically collaborate with clinical data management and biostatistics teams during a study?

As a Contract Medidata Rave Programmer, you will regularly interface with clinical data managers and biostatisticians to ensure that electronic data capture (EDC) systems meet protocol specifications and study requirements. You’ll participate in requirements gathering, review case report forms (CRFs), and address data validation needs, often through meetings and collaborative platforms. Effective communication and responsiveness are crucial, as you may need to troubleshoot issues, implement mid-study changes, or clarify data logic to support study timelines. This collaborative environment helps ensure high-quality data collection and smooth study execution.

What is a Contract Medidata Rave Programmer?

A Contract Medidata Rave Programmer is an information technology specialist hired on a temporary or project basis to design, configure, and maintain clinical trial databases using Medidata Rave, a leading electronic data capture (EDC) system in the pharmaceutical and biotechnology industries. Their responsibilities typically include creating electronic Case Report Forms (eCRFs), managing edit checks, programming custom data exports, and supporting data validation activities. These programmers collaborate closely with data managers, clinical teams, and statisticians to ensure that clinical data is accurately captured and compliant with regulatory standards.

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

AspectContract Medidata Rave ProgrammerClinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, Clinical Research, or related field; experience with Medidata RaveBachelor's in Nursing, Life Sciences, or related; familiarity with clinical data management
Work EnvironmentContract-based, primarily remote or on-site at clinical trial sites or CROsTypically on-site at clinical research sites or hospitals, coordinating data collection
Employer & Industry UsagePharmaceutical companies, CROs, clinical research organizationsHospitals, research institutions, pharmaceutical companies

The Contract Medidata Rave Programmer focuses on configuring and maintaining electronic data capture systems using Medidata Rave, while the Clinical Data Coordinator manages data collection and quality at clinical sites. Both roles require knowledge of clinical data processes but differ in technical versus operational focus.

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Contract Medidata Rave Programmer jobs near you
Infographic showing various Contract Medidata Rave Programmer job openings in the United States as of May 2026, with employment types broken down into 66% Full Time, 7% Part Time, and 27% Contract. Highlights an 80% In-person, 7% Hybrid, and 13% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Lead Clinical Data Manager

Katalyst Healthcares and Life Sciences

Boulder, CO

Full-time

Posted 28 days ago

Job description

Responsibilities:
  • Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards.
  • Provide strategic oversight and direction to CRO clinical data management teams for assigned studies.
  • Develop and implement data management plans, case report forms (CRFs), edit checks, and data validation plans in alignment with study protocols and regulatory requirements.
  • Oversee the design, build, and validation of clinical databases using Medidata Rave EDC, ensuring optimal configuration and functionality.
  • Conduct thorough reviews of clinical data, identifying trends, inconsistencies, and potential issues that may impact data quality or study outcomes.
  • Collaborate with cross-functional teams including Biostatistics, Clinical Operations, Safety, and Regulatory to ensure alignment of data management strategies with overall clinical development goals.
  • Provide oversight, and performance management of external data management vendors.
  • Maintain SOPs, guidelines, and best practices for clinical data management processes.
  • Represent the Clinical Data Management function in internal and external meetings, providing expert guidance on data-related matters.
  • Stay current with industry trends, regulatory requirements, and technological advancements in clinical data management, particularly in the oncology field.
Requirements:
  • Bachelor's degree in Life Sciences, Computer Science, or a related field; advanced degree preferred.
  • minimum of 7+ years of clinical data management experience in the biotechnology or pharmaceutical industry.
  • Experience managing oncology clinical trials data, including a deep understanding of oncology-specific data requirements and challenges.
  • Expert-level proficiency with Medidata Rave EDC, including system configuration, form design, and edit check programming.
  • Strong knowledge of clinical research processes, FDA & ICH guidelines, GCP, GCDMP, and CDISC standards.
  • Demonstrated experience in CRO and vendor oversight.
  • Excellent project management skills with the ability to manage multiple studies simultaneously.
  • Strong analytical and problem-solving skills with meticulous attention to detail.
  • Outstanding communication and interpersonal skills, with the ability to effectively collaborate with diverse stakeholders.
  • Proficiency in Microsoft Office Suite and familiarity with statistical software (e.g., SAS, R) is a plus.
  • CCDM (Certified Clinical Data Manager) certification.
  • Experience with risk-based monitoring in oncology studies.
  • Knowledge of emerging technologies in clinical data collection and management (e.g., ePRO, wearables, AI/ML applications).

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