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Contract Medidata Rave Programmer Jobs (NOW HIRING)

MediData

Senior Applications Engineer

Woodbridge, NJ · On-site

$114.75 - $153/hr

Medidata follows a hybrid office policy in which employees who are hired for an in-person position ... Strong presentation and communication skills, including development of service contracts * Basic ...

Cytokinetics

Contract Clinical Systems Specialist

$75 - $86/hr

Bachelor's degree in information technology, computer science, computer engineering, statistics, or ... Experience with EDC (Medidata Rave) and/or clinical data repository (CDR) systems * Experience with ...

Medidata Solutions

Senior Applications Engineer

Iselin, NJ · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... Strong presentation and communication skills, including development of service contracts Your ...

BeiGene USA

Manager, EDC Administration

Cambridge, MA · On-site +1

$136K - $165K/yr

Master's degree (or its foreign degree equivalent) in Computer Science, Engineering (any field), or ... Special Skill Requirements: (1) Experience with Clinical Systems (Medidata Rave, Oracle Inform ...

Synectics Inc

Systems Designer / Analyst

Somerville, NJ

$50.34 - $62.93/hr

Experience with technical study build in Medidata RAVE is required. * Veeva EDC technical study ... ing, finance, healthcare, and professional services recruitment, offering both contract and ...

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

As of Aug 21, 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 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.

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 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.

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 August 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 69% In-person, and 31% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Associate Director (Multiple Positions) | ZR_880_JOB

Agilisium

Westlake Village, CA • On-site

$160K/yr

Full-time

Posted 10 days ago

Job description


TITLE:Associate Director (Multiple Positions)
LOCATION:Westlake Village, CA and various and unanticipated locations throughout the U.S. (Must be willing to work anywhere in the U.S. as the position may involve relocation to various and unanticipated client site locations; any relocation to be paid by employer pursuant to internal policy.)
DUTIES:Develop and implement CSV/CSA strategies ensuring compliance with GxP, 21 CFR Part 11, Annex 11, GAMP 5, and data-integrity requirements. Serve as subject matter expert providing technical and regulatory guidance for compliant system design and lifecycle controls. Oversee lifecycle validation activities for GxP systems including implementation, configuration changes, reviews, and decommissioning. Lead impact assessments to maintain regulatory and quality-system compliance. Author, review, and approve validation and quality deliverables. Maintain and enhance distribution quality-management processes to ensure adherence to applicable GxP regulations and international standards. Optimize distribution and quality-related technologies to strengthen data integrity, traceability, audit readiness, and operational performance within regulated environments. EOE
REQTS:Must have a Bachelor's degree or foreign equivalent in Information Technology, Computer Science, or a related field plus five (5) years of experience in the position offered, as a Test Lead Validation Engineer, or a related position. Must have five (5) years of experience with all of the following:Designing ILM-driven data management architectures in Informatica to support regulated-data protection and compliance through standardized archiving, masking, and validation methodologies; Designing enterprise information governance frameworks on OpenText platforms in accordance with regulatory requirements by applying standardized discovery, classification, retention, and disposition controls that support GDPR, HIPAA, and SOX compliance; Engineering clinical-data management architectures across Oracle Inform, Oracle IRT, and Medidata Rave platforms in alignment with validated design, coding, and review methodologies to support study accuracy and regulatory compliance; Designing DocuSign-based electronic signature architectures in alignment with 21 CFR Part 11 through the application of standardized configuration and validation methodologies; Engineering governed BI architectures that support validated analytics and secure access controls across MicroStrategy and Cognos platforms through standardized modeling, performance-tuning, and verification methodologies; Leading GxP compliance initiatives by applying advanced CSV and SDLC validation methodologies incorporating risk-based assessment, controlled documentation practices, and regulatory-aligned lifecycle standards; and Managing quality system governance within ServiceNow by applying 21 CFR Part 11 compliant change management and deviation control frameworks aligned with GAMP 5 validation principles.
HOURS:Full-Time; Mon-Fri (40 hrs/week)
SALARY:$160,000 - $160,000 per year

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