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Medidata Rave Custom Function Programmer Jobs (NOW HIRING)

Clinovo

Sr Clinical Data Manager

Waltham, MA · On-site

Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical ... Strong Medidata Rave experience required. * Expert knowledge of Electronic Data Capture (EDC ...

CYNET SYSTEMS

Clinical Data Management Analyst

Irvine, CA · On-site

$38 - $43/hr

Experience with EDC (Electronic Data Capture) systems required, both Classic and New Medidata RAVE ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

New

CYNET SYSTEMS

Clinical Data Management Analyst

Irvine, CA · On-site

$38 - $43/hr

Experience with EDC (Electronic Data Capture) systems required, both Classic and New Medidata RAVE ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

New

Cynet Systems

Clinical Data Management Analyst

Irvine, CA · On-site

$38.76 - $43.76/hr

Experience with EDC (Electronic Data Capture) systems required, both Classic and New Medidata RAVE ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

New

Medidata Solutions

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

The AI features developed will power modern clinical trial study design and study conduct with Rave ... roles, Medidata sets ranges based on a number of factors including function, level, candidate ...

MediData

Senior Data Scientist

Manhattan, NY · On-site

$114K - $153K/yr

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 ...

Immunocore

$121K - $202K/yr

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

MediData

Technical Support Engineer

Woodbridge, NJ · On-site

$79K - $106K/yr

The Technical Support Engineer will handle work requests directly, or solicit assistance from the ... As with all roles, Medidata sets ranges based on a number of factors including function, level ...

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All JobsMedidata Rave Custom Function Programmer Jobs

Medidata Rave Custom Function Programmer information

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How much do medidata rave custom function programmer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for medidata rave custom function 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 Medidata Rave Custom Function Programmer?

A Medidata Rave Custom Function Programmer is a specialized professional who develops, maintains, and implements custom functions within the Medidata Rave electronic data capture (EDC) system. These custom functions are typically written in Rave’s proprietary language (Rave Architect or C#) and are used to automate complex data validations, calculations, and workflow processes for clinical trials. Their work ensures that study data is collected accurately and efficiently, supporting regulatory compliance and study integrity. These programmers often collaborate with clinical data managers, database designers, and other stakeholders to tailor the Rave environment to specific study needs.

What are the key skills and qualifications needed to thrive as a Medidata Rave Custom Function Programmer?

To thrive as a Medidata Rave Custom Function Programmer, you need a strong background in clinical data management, programming (especially C# or JavaScript), and experience with Medidata Rave EDC systems. Familiarity with Medidata Rave architecture, custom function development, and regulatory compliance such as 21 CFR Part 11 is typically required, along with relevant Medidata certifications. Strong problem-solving abilities, attention to detail, and effective communication skills are crucial for translating study requirements into reliable technical solutions. These competencies ensure accurate study setup, regulatory compliance, and efficient clinical trial data management.

What are some common challenges Medidata Rave Custom Function Programmers face when integrating custom logic into clinical trial databases?

Medidata Rave Custom Function Programmers often encounter challenges such as ensuring custom functions are validated and compliant with regulatory standards, troubleshooting complex logic errors, and maintaining compatibility with evolving Medidata platform updates. Coordination with data managers and clinical teams is crucial to accurately interpret protocol requirements and translate them into functional code. Additionally, balancing multiple project timelines and adapting to rapidly changing study needs requires strong organizational and communication skills.

What are popular job titles related to Medidata Rave Custom Function Programmer jobs?

For Medidata Rave Custom Function Programmer jobs, the most frequently searched job titles are:

Infographic showing various Medidata Rave Custom Function Programmer job openings in the United States as of September 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Sr Clinical Data Manager

Waltham, MA • On-site

Clinovo
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Clinovoexternal

Contractor

Posted 10 days ago

Job description

Position Overview
A clinical-stage biotechnology company is seeking an experienced Senior Clinical Data Manager Consultant to support its growing clinical development organization.
The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will play a key role in developing and executing clinical data strategies that support high-quality, regulatory-compliant data deliverables.
The ideal candidate will bring significant sponsor-side clinical data management and vendor/CRO oversight experience, along with strong hands-on expertise with Medidata Rave.
This is a senior-level position requiring the ability to independently manage complex data management activities, identify and resolve issues, and effectively collaborate with Clinical Operations, Biostatistics, Statistical Programming, and other cross-functional stakeholders.
Key Responsibilities
  • Lead Clinical Data Management activities across assigned clinical trials from study start-up through database lock.
  • Develop and oversee eCRFs, eCRF completion guidelines, Data Management Plans (DMPs), data review guidelines, edit check specifications, and other study-specific data management documentation.
  • Design, review, and finalize case report forms (CRFs) in collaboration with cross-functional team members.
  • Oversee the implementation and maintenance of study-specific clinical data management systems and processes.
  • Lead and oversee database development, validation, user acceptance testing (UAT), and go-live activities.
  • Develop and execute plans for the processing, review, and cleaning of clinical trial data within established timelines and budgets.
  • Monitor clinical data flow and ensure timely, accurate, and high-quality data availability for analysis.
  • Identify data quality issues and work with internal teams and external partners to drive timely resolution.
  • Provide strong sponsor oversight of CROs, data management vendors, and other external partners responsible for outsourced data management activities.
  • Establish and monitor vendor performance, timelines, deliverables, and data quality expectations.
  • Review clinical protocols and Statistical Analysis Plans (SAPs) to ensure alignment with data collection and management requirements.
  • Ensure clinical data management activities comply with applicable SOPs, ICH-GCP, regulatory requirements, and industry standards.
  • Represent Clinical Data Management in cross-functional study team meetings.
  • Communicate project status, risks, issues, and proposed resolutions to project teams and leadership.
  • Provide recommendations regarding clinical data management processes, systems, and study-specific challenges.
  • Contribute to the continued development and improvement of data management processes, standards, and tools.
  • Monitor study-related data management budgets and evaluate vendor change orders and potential cost overruns.
  • Support audits and regulatory inspections and contribute to corrective and preventive action (CAPA) activities when required.
  • Train and mentor junior team members and promote clinical data management best practices.
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical, Regulatory, and other functional stakeholders.
Required Experience & Qualifications
  • Bachelor's degree in a scientific, clinical, life sciences, or related discipline.
  • Minimum of 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
  • Strong sponsor-side experience, including direct oversight of CROs and external data management vendors.
  • Extensive experience leading Clinical Data Management activities across the full clinical trial lifecycle, from study start-up through database lock.
  • Strong Medidata Rave experience required.
  • Expert knowledge of Electronic Data Capture (EDC) systems; experience with platforms such as Medidata Rave and Veeva.
  • Significant experience with database design, development, validation, and user acceptance testing.
  • Strong understanding of CDISC standards, including CDASH and SDTM.
  • Strong knowledge of ICH-GCP, FDA requirements, and other applicable clinical trial regulations and guidelines.
  • Expert understanding of clinical trial processes, clinical data flow, data review, and data cleaning best practices.
  • Demonstrated experience managing CROs, vendors, and global clinical study teams.
  • Proven ability to lead data management activities for complex and/or global clinical trials.
  • Ability to independently identify and resolve complex data management and technical issues.
  • Strong project management, organizational, and prioritization skills.
  • Excellent written and verbal communication skills.
  • Ability to effectively influence cross-functional stakeholders and senior leadership.
  • Ability to manage multiple priorities and studies within a fast-paced clinical development environment.
Key Candidate Profile
The strongest candidates will combine deep clinical data management expertise with significant sponsor-side oversight experience. Candidates should be comfortable operating independently, managing CRO and vendor deliverables, and serving as the Clinical Data Management subject matter expert within a cross-functional study team.
Medidata Rave expertise and strong sponsor oversight experience are critical requirements for this position.

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