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Clinical Programmer Medidata Rave Jobs (NOW HIRING)

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Clinical data review and listing experience (Preferably Medrio, Medidata Rave). * Excellent ... Excellent hands on experience on SAS or R programming language for data review listings/tracker.

Mercor

Drug Discovery Specialist - AI Trainer

San Jose, CA · On-site +1

$1.1K - $1.4K/wk

Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , and Benchling . * Design multi-step tasks grounded in your real workflows. Require navigating multiple apps, files ...

New

Cape Fox SS

Research Database Developer

Cincinnati, OH · Remote

$90K - $120K/yr

... within clinical research settings. The ideal candidate will possess proficiency in programming ... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ...

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115K - $150K/yr

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Medidata Rave preferred). * Solid understanding of clinical trial processes and data flow.

Vor Bio

Senior Data Manager

Boston, MA · On-site

... programming. Suggest design for standard and non-standard data collection, identify any gaps in ... clinical data management systems and/or EDC products e.g. Medidata Rave. Must have Medidata RAVE ...

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Clinical Programmer Medidata Rave information

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

As of Jun 15, 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 in the Clinical Programmer Medidata Rave position, and why are they important?

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 job?

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 June 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Associate Director, Clinical Data Programmer

Associate Director, Clinical Data Programmer

Amylyx Pharmaceuticals

Cambridge, MA • Remote

Other

Posted 11 days ago

Job description

The Opportunity

The Clinical Data Management team at Amylyx Pharmaceuticals is seeking an Associate Director, Clinical Data Programmer. This individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. As an Associate Director of Clinical Data Programming, you will be required to program in the appropriate languages to create both textual and graphic displays that facilitate data cleaning and review.

Responsibilities

  • Lead the study-specific design, development, and validation of study clinical data capture systems, ensuring data integrity, CDISC compliance and CRO oversight.
  • Supports leading data management activities (i.e. DMP creation, CRF creation, edit checks creation, database lock), assisting with database setup, conduct and closeout phases.
  • Performs UAT of systems and ensures appropriate plans and documentation are in place.
  • Leads the development of SAS macros, data listings, summary tables and visualizations for supporting periodic and ad hoc data review.
  • Manages external vendor compliance and quality checks.
  • Supports Clinical Operations, Biostatistics and Data Management by providing data insight and solving technical data challenges.
  • Ensures databases adherences to SOPs, 21CRF Part 11, ICH-GCP and CDISC Standards (CDASH/SDTM)
  • Acts as a subject matter expert in leading technical initiatives and data management

Required Qualifications

  • Bachelor's degree or higher in Life Science or related discipline
  • 8+ years of experience in clinical data management
  • Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python
  • Proven experience in clinical trial programming and database management
  • Knowledge of Clinical Data Standards such as CDISC CDASH, and SDTM
  • Provide strong support to Data Management
  • Experience creating advanced interactive data visualizations from raw data using multi-languages and applications such as Using SAS, R, Python, RShiny, Power BI, Tableau, Spotfire etc.
  • Ability to manage multiple projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change.
  • Excellent written and verbal communication skills and organizational and documentation skills.

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested, which may include travel by air, driving or public transportation.
  • You must have access to work in setting that meets all requirements of the role (including privacy, reliable internet access, phone, ability to communicate via video conference, etc.) at your remote locatio

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