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Freelance Clinical Programmer Medidata Rave Jobs

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

Prometrika LLC

Senior Clinical Data Manager

Cambridge, MA · On-site

$144K - $167K/yr

Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies * Lead ... Expertise with EDC systems, such as Medidata Rave, InForm, Medrio * Excellent organizational and ...

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

As of Jun 17, 2026, the average hourly pay for freelance 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 as a Freelance Clinical Programmer specializing in Medidata Rave, and why are they important?

To excel as a Freelance Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, database design, and programming—often backed by a degree in life sciences, computer science, or a related field. Expertise in Medidata Rave EDC, CDISC standards (SDTM, CDASH), and relevant programming languages like SQL or SAS is typically required, along with certifications in Medidata Rave. Strong attention to detail, problem-solving abilities, and effective communication with cross-functional teams are vital soft skills. These competencies ensure efficient, compliant clinical trial data handling and facilitate seamless collaboration in a highly regulated environment.

What does a Freelance Clinical Programmer specializing in Medidata Rave do?

A Freelance Clinical Programmer with expertise in Medidata Rave is responsible for designing, programming, and maintaining electronic data capture (EDC) systems for clinical trials using the Medidata Rave platform. Their tasks include building and validating study databases, creating eCRFs (electronic Case Report Forms), programming edit checks, and ensuring data integrity and compliance with regulatory standards. As freelancers, they typically work on a contract basis for pharmaceutical companies, CROs, or research organizations, and must stay updated on both industry regulations and the latest Medidata Rave functionalities.

What are some typical challenges a Freelance Clinical Programmer faces when working with Medidata Rave, and how can they be managed?

Freelance Clinical Programmers working with Medidata Rave often encounter challenges such as understanding complex study protocols, handling tight timelines, and ensuring accurate data mapping across multiple studies. Since freelancers may not have immediate access to on-site teams, effective remote communication and documentation are crucial for resolving queries with data managers and sponsors. Staying updated with Medidata Rave's latest features and maintaining strong organizational skills can help manage these challenges efficiently and deliver high-quality results.
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Freelance Clinical Programmer Medidata Rave jobs near you
Infographic showing various Freelance Clinical Programmer Medidata Rave job openings in the United States as of June 2026, with employment types broken down into 82% Full Time, 9% Part Time, and 9% Contract. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Lead Clinical Research Associate

Lead Clinical Research Associate

Integrated Resources INC

Raritan, NJ

Full-time

Posted 11 days ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Title: Lead Clinical Research Associate

Location: Raritan, NJ 08869

Responsibilities: 

LEAD CLINICAL RESEARCH ASSOCIATE:

Under supervision of Clinical Project Lead, oversees performance of assigned field monitors and site activities in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal regulations.

The LCRA acts as a primary liaison between Field Based CRAs and the Clinical Project Lead (CPL).

Additional responsibilities include:

Implementation of enrollment and recruitment strategies

Assistance in vendors' selection processes

Development, execution, management and compliance assurance of the Monitoring Plan

Review and approve trip reports, track scheduling, report submission metrics, site deviations and action items

Oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions.

Development of training materials and study tools for site and CRA use

Assistance in formation of the Adjudication Committee including oversight of documentation collection and filing into the Trial Master File

Qualifications

Qualifications:
LEAD CLINICAL RESEARCH ASSOCIATE:

BS/BA, MS is desirable

5+ years of site management of which a minimum of 2 years field monitoring experience

Knowledge of applicable standards and regulations for clinical trial

Proven oral and written communication skills

Proven planning skills; ability to create and track detailed project plans

Proven interpersonal, leadership, organizational and effective time management skills

Microsoft Office proficiency

Ability to work independently and within a cross-functional team environment to identify and escalate site/monitoring related activities issues to the management team in a timely fashion

Experience in Cardiovascular Therapeutic area

IVD Stud Experience

Medidata RAVE system 

Additional Information

Kind Regards,

Sabanaaz Shaikh

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Gold Seal JCAHO Certified for Health Care Staffing

"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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