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How much do part time medidata rave programmer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for part time 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 part time Medidata Rave programmer?

A Part Time Medidata Rave Programmer is a professional who works on a part-time basis to configure, customize, and maintain electronic data capture (EDC) systems using Medidata Rave for clinical trials. They create and modify study databases, build case report forms (CRFs), and ensure that data is collected and managed according to study protocols. These programmers collaborate with clinical teams and data managers to support data integrity and regulatory compliance throughout the clinical trial process.

What are the typical responsibilities and challenges faced by a part time Medidata Rave programmer in a clinical research setting?

As a Part Time Medidata Rave Programmer, you will primarily be responsible for building and maintaining electronic data capture (EDC) systems within the Medidata Rave platform to support clinical trials. Common tasks include designing case report forms (CRFs), programming edit checks, and ensuring data integrity and compliance with regulatory standards. A key challenge is effectively managing multiple projects on a part-time schedule, which requires strong time management and communication skills to coordinate with data managers, clinical teams, and other programmers. Additionally, you may need to quickly adapt to evolving protocol changes and troubleshoot system issues to meet study timelines.

What are the key skills and qualifications needed to thrive as a part time Medidata Rave programmer, and why are they important?

To thrive as a Part Time Medidata Rave Programmer, you need a solid understanding of clinical data management, database programming, and experience with Medidata Rave, often requiring a degree in life sciences or a related field. Familiarity with EDC systems, Medidata Rave configuration tools, and certifications such as Medidata Rave Study Builder are highly valued. Attention to detail, problem-solving abilities, and effective communication are essential soft skills for collaborating with cross-functional teams and ensuring data integrity. These skills ensure accurate study builds, regulatory compliance, and efficient clinical trial data management.
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Part Time Medidata Rave Programmer jobs near you
Infographic showing various Part Time Medidata Rave Programmer job openings in the United States as of September 2026, with employment types broken down into 89% Full Time, 3% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Psychiatrist / Sub-Investigator - Clinical Research (Part-Time, NYC)

New York, NY

Fieve Clinical Research
Pharmaceutical and Medicine Manufacturing • 1 - 10 employees
Learn more about Fieve Clinical Researchexternal

$100 - $200/hr

Full-time, Part-time

Posted 9 days ago

Job description

Fieve Clinical Research is seeking a second board-certified physician to serve as Sub-Investigator (Sub-I) or Co-Principal Investigator on active and upcoming Phase II-IV clinical trials in psychiatry and neurology. This is an ideal fit for a psychiatrist, neurologist, or internist - including residents, academic faculty, or clinicians transitioning from industry - who wants to stay connected to drug development without a full-time research commitment.

About Us Founded on the legacy of Ronald R. Fieve, MD - the Columbia University psychiatrist who established lithium therapy for bipolar disorder in the U.S. - Fieve Clinical Research has been part of Manhattan's clinical research landscape for more than 40 years. Our investigators have conducted 125+ trials across psychiatry, neurology, pain management, and internal medicine, working with major pharmaceutical sponsors and leading CROs including IQVIA and ICON.

What You'll Do

  • Serve as Sub-I or Co-PI on industry-sponsored outpatient trials (MDD, GAD, TRD, PTSD, migraine, fibromyalgia, and more)

  • Conduct protocol-specified medical/psychiatric evaluations and administer validated rating scales (MADRS, HAM-D, CGI, MIDAS, HIT-6)

  • Review subject eligibility, informed consent, and safety decisions

  • Identify and report adverse events per FDA/ICH-GCP requirements

  • Maintain GCP-compliant source documentation

  • Participate in site initiation visits, monitoring visits, and audits as assigned

  • Partner with the PI and Site Director on feasibility and enrollment strategy

  • Provide mentorship to study coordinators as your involvement grows

Why This Role

  • Minimum 1 day/week, Saturdays available - built around your existing clinical or academic schedule

  • No prior research experience required - we provide GCP training and mentorship

  • Authorship and CV-building potential on active industry trials

  • Direct path into psychopharmacology research at a site with a 40-year track record

Qualifications - Required

  • MD or DO from an accredited medical school

  • Active, unrestricted New York State medical license

  • Board certified or board eligible (NY) in Psychiatry, Neurology, or a closely related specialty; internists also considered

  • Ability to commit to a minimum of 1 on-site day/week in Midtown Manhattan

  • Baseline familiarity with clinical trial regulatory requirements (FDA, IRB, informed consent)

  • ICH-GCP certification preferred but not required - we support training/renewal

Qualifications - Preferred

  • 1-3+ years as a sub-investigator or investigator on industry-sponsored trials (not required - training provided)

  • Experience with MDD, bipolar disorder, schizophrenia, migraine, or epilepsy

  • Existing DEA registration, or willingness to obtain

  • Spanish language proficiency

  • Familiarity with EDC systems (Medidata Rave, Oracle InForm, REDCap)

Fieve Clinical Research is an Equal Opportunity Employer. All qualified applicants will receive consideration regardless of race, color, religion, sex, national origin, disability, or veteran status.

HOW TO APPLY

Please send your CV/biosketch, a brief cover note on your research background and therapeutic interests, and confirmation of your NY license/board status to:

Liana Slater, Operations - liana.slater@fieveclinical.com (347) 281-3998 | fieveclinicalresearch.com

Compensation Information:
$100.00 / Hourly - $200.00 / Hourly

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