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Freelance Clinical Programmer Medidata Rave Jobs in Ohio

$39K - $51K/yr

Life Sciences, Medical, Clinical trials, etc. Please note that this is a remote, freelance ... Developers around the world. Earn money. Have fun. Advance human knowledge. Work on diverse ...

Freelance Clinical Programmer Medidata Rave information

What are the key skills and qualifications needed to thrive as a freelance clinical programmer Medidata Rave?

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 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 Medidata Rave 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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What job categories do people searching Freelance Clinical Programmer Medidata Rave jobs in Ohio look for? The top searched job categories for Freelance Clinical Programmer Medidata Rave jobs in Ohio are:
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Infographic showing various Freelance Clinical Programmer Medidata Rave job openings in Ohio as of August 2026, with employment types broken down into 78% Full Time, 4% Temporary, and 18% Contract. Highlights an 79% In-person, and 21% Remote job distribution.

Clinical Research Professional / Clinical Research Professional II, UC Cancer Center

University of Cincinnati

Cincinnati, OH • On-site

$23.25 - $31/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 22 days ago


University Of Cincinnati rating

7.4

Company rating: 7.4 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

337th of 617 rated colleges and universities


Job description

Clinical Research Professional / Clinical Research Professional II, UC Cancer Center
Posting Start Date: 5/18/26
Work Arrangement: Onsite
Current UC employees must apply internally via SuccessFactors
Next Lives at the University of Cincinnati
Founded in 1819, the University of Cincinnati ranks among the nation's best urban public research universities. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called "the most ambitious campus design program in the country." UC's momentum has never been stronger as the anchor of the Cincinnati Innovation District, the oldest cooperative education (co-op) program in the country with students earning $94 million annually through paid experiences, an academic health system, and as a member of the Big 12 Conference. The university contributes $10.6 billion in economic impact to the city and $22.7 billion to the state of Ohio. At UC, next is all of us. Learn more at uc.edu.
UC is a mission-driven organization where we are committed to student success and positively transforming the community through scholarship and service. We thrive on innovation, making an impact, and fostering an environment where staff and faculty are key contributors to UC's success.
Job Overview
As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. In partnership with the UC Health academic healthcare system and Cincinnati Children's Hospital Medical Center, College of Medicine's faculty are transforming the world of medicine every day.
The University of Cincinnati Cancer Program is looking to fill a patient facing position as either a Clinical Research Professional or Clinical Research Professional II. This position will support the University's mission and commitment to excellence in our students, faculty, staff and all our activities.
Please note this is a FULL-TIME, ON-SITE position, with incidental work from home opportunities.
Essential Functions
Under general supervision of the Clinical Research Manager, the Clinical Research Professional provides data management support and assistance to the University of Cincinnati Cancer Center Clinical Trials Office. Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum.
  • Follow established CTO workflows and CTO/UC Health standard operating procedures.
  • Proactively review and locate source documentation for all study procedures.
  • Accurately enters data from source documentation into electronic data capture (EDC) systems within 5 days of the patient visit.
  • Proactively seeks to promptly resolve outstanding data queries and any issues through collaboration with clinical research coordinators (CRCs).
  • Maintains and uses organizational systems to avoid delinquent data entry.
  • Reviews all data entered into EDCs and subject charts to identify and help resolve any general quality issues.
  • Conducts study participant follow-up as required per protocol.
  • Communicates and collaborates within assigned research team and with principal investigators in a professional, helpful, and service-oriented manner.
  • Acts as the primary point of contact for monitoring visits
  • Adheres to all UCCC CTO work instructions, SOPs, and study specific timeframes.
  • Able to independently maintain and meet form & database development milestones.
  • Maintain/Update patients' status in the Clinical Trial Management System.
  • Maintain Team's biospecimen collection kit inventory, re-ordering supplies as needed.

Minimum Requirements
Clinical Research Professional:
  • Bachelor's Degree must be in a related field.
  • Five (5) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.
  • One (1) year of related experience.

Clinical Research Professional II:
  • Bachelor's Degree must be in a related field.
  • Seven (7) years of relevant work experience and /or other specialized training can be used in lieu of education requirement.
  • Three (3) years of related experience.

Additional Qualifications Considered
  • Prior experience in clinical research coordination or clinical research data management, and SignalPath, Complion, RedCap, Inform, Medidata RAVE, etc. systems is ideal.
  • Highly comfortable with computer-based and online systems
  • Must be able to interact and communicate with clinical research staff, PIs, and industry sponsors in a professional manner.
  • High attention to detail and organizational ability and ability to prioritize tasks.
  • Can accomplish work independently.
  • Capable of advising and explaining information to others.
  • Ability to manage moderately complex projects.
  • Working knowledge of, and ability to apply, Good Documentation Practices, ALCOA, and ICH-GCP to data management and database design.
  • Adherence to core values that were designed to create and maintain a positive work environment: Respect, Integrity, Teamwork and Excellence.

Physical Requirements/Work Environment
  • Office environment/no specific unusual physical or environmental demands.

Compensation and Benefits
UC offers an exceptional benefits package designed to support your well-being, financial security, and work-life balance. (UC Benefits) Eligibility may vary by position and FTE status. Highlights include:
Salary/Hourly Pay Rate Information:
Comprehensive Tuition Remission
UC provides tuition remission for you and your eligible dependents, covering tuition costs for nearly all undergraduate and graduate programs offered by the university.
Robust Retirement Plans
As a UC employee, you won't contribute to Social Security (except Medicare). Instead, you'll choose between state pension plans (OPERS, STRS) or an Alternative Retirement Plan (ARP), with UC contributing 14-18% of your salary based on position.
Real Work-Life Balance
UC prioritizes work-life balance with a generous time-off policy, including:
Vacation and sick time
11 paid holidays and additional end-of-year paid time off (Winter Season Days)
6 weeks of paid parental leave for new parents
Additional Benefits Include:
  • Competitive salary based on experience
  • Comprehensive health coverage (medical, dental, vision, prescription)
  • Flexible spending accounts & wellness programs
  • Professional development & mentorship opportunities

To learn more about why UC is a great place to work, please visit our Careers Page.
UC is an E-Verify employer. If hired into this position, you will be required to provide satisfactory proof of employment eligibility by providing acceptable, original forms of identification for employment verification via the Federal I-9 employment verification process. Click here for a list of acceptable documents.
Important: To apply you must create a profile and submit a complete job application through the UC applicant portal. We are unable to consider "easy apply" applications submitted via other websites. For questions about the UC recruiting process or to request accommodations with the application, please contact UC HR at jobs@uc.edu.
Equal Opportunity Employer. Building a workplace where all qualified applicants will receive consideration for employment, including Individuals with Disabilities and Protected Veterans.
REQ: 101638

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