1

Medidata Rave Jobs in Philadelphia, PA (NOW HIRING)

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

Strong technical skills with experience in EDC systems and data management tools (e.g., Rave, Inform, Medidata). * Excellent communication, leadership, and problem-solving skills with the ability to ...

Medidata Rave information

See Philadelphia, PA salary details

$29

$61

$88

How much do medidata rave jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for medidata rave in Philadelphia, PA is $61.24, according to ZipRecruiter salary data. Most workers in this role earn between $51.29 and $69.68 per hour, depending on experience, location, and employer.

What is a Medidata Rave?

A Medidata Rave job typically involves working with Medidata Rave, a widely used electronic data capture (EDC) system in clinical trials. Professionals in this role manage study databases, design case report forms (CRFs), ensure data integrity, and support clinical research teams. Roles may include Rave Study Builder, Data Manager, or Clinical Programmer. Strong knowledge of clinical trial processes, database management, and SQL is often required.

What are the key skills and qualifications needed to thrive in the Medidata Rave position, and why are they important?

To thrive as a Medidata Rave specialist, you need a solid understanding of Electronic Data Capture (EDC) systems, clinical data management, and regulatory guidelines, typically supported by certifications in Medidata Rave or relevant clinical research fields. Proficiency with the Medidata Rave platform, user administration, and familiarity with tools such as SQL or other database management systems are highly valued. Strong attention to detail, communication, and problem-solving skills help professionals stand out in this role. These qualities ensure accurate data collection, regulatory compliance, and effective collaboration in complex clinical trial environments.

What are some common challenges faced by Medidata Rave specialists in clinical trials?

Medidata Rave specialists often encounter challenges such as ensuring data accuracy across multiple sites, managing complex study protocols, and troubleshooting technical issues within the platform. They are responsible for configuring case report forms, supporting site users, and maintaining regulatory compliance, which requires constant vigilance and adaptability. Collaboration with clinical research teams, sponsors, and IT staff is vital to address study-specific needs and resolve problems efficiently. These challenges make the role dynamic but also provide opportunities for continuous learning and professional growth.

Infographic showing various Medidata Rave job openings in Philadelphia, PA as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $127,381 per year, or $61.2 per hour.

Medidata Rave | Clinical Programmer (Remote, Full Time)-LC0002

TechData Service Company LLC

King Of Prussia, PA • Remote

$90K - $150K/yr

Full-time

Medical, Dental, Retirement, PTO

Posted 6 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.


Job description

Qualifications:

•5+ years of EDC database build experience for clinical trial.

•Experience with Medidata Rave with Medidata certification; Minimum two to three years current database programming experience designing studies and data validation programming in Medidata Rave.

•Is able to write the code at CF from scratch.

•Familiarity with clinical data regulations (GCP, ICH).

•Familiarity with Operational Qualification/Performance Qualification and UAT execution and documentation.

•BS or MS degree in related discipline.

Responsibilities:

•Build and design clinical study trials in Medidata RAVE system.

•Design/create and test clinical databases including forms, folders, matrices, data

dictionaries/code lists, unit dictionaries, edit checks/rules, derivations, custom functions, standard and custom reports.

•Provide programming expertise to support data capture, review, and monitoring for clinical trials.

•Program reports, edit checks, and custom functions based on study protocol requirements.

•Assist with EDC integration with other systems, including but not limited to IRT system, CTMS system and etc.

•Manage external vendor data import and validation.

•Provide technical support as needed for Medidata RAVE and Merative Zelta EDC systems.

•Participate in EDC design requirements development in collaboration with Study Lead Data Manager and the wider study team.

•Support development of and updates of global library objects as appropriate according to best practices and new standards.

•Perform peer review for the studies built by other programmers.

•Maintain all required Clinical Systems study documentation.

•Provide EDC technical support to facilitate study timelines and deliverables.

•Manage timely-quality deliverables for the study teams for assigned protocol/study(s).

TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Company Description

https://quantive.bio/