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Entry Level Clinical Programmer Medidata Rave Jobs

3ds

Data Scientist

New York, NY · On-site

$96K - $128K/yr

The AI features developed will power modern clinical trial study design and study conduct with Rave ... Medidata believes that benefits should connect you to the support you need when it matters most and ...

Denali Health

Research Assistant

Plant City, FL · On-site

$16.75 - $23.25/hr

Exposure to clinical research (eSource/eCRF; Medidata Rave or REDCap). * Familiarity with ICH-GCP, SOPs, CLIA. * Bilingual (especially Spanish/English). How we will support your growth * 30-60-90 day ...

Lumos Pharma

Data Manager

Medidata Rave EDC System experience * SAS experience * Experience with CDISC standards (e.g. SDTM ... clinical trials * Independent proficiency in programming data management * Microsoft Power BI ...

3ds

Solution Sales Specialist, Data Experience

New York, NY · On-site

$116K - $155K/yr

... Engineering. The Solution Sales Specialist, Clinical Data Studio, will shape and help implement Medidata's go-to-market strategy for data review, quality, and all other Clinical Data Studio (CDS ...

3ds

Senior Training Specialist (Remote)

New York, NY · On-site +1

$84K/yr

... developer, and the ability to work across teams to transform Medidata's instructor-led training experience. The ideal candidate has a solid life sciences or clinical trial operations background ...

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As of Jun 5, 2026, the average hourly pay for entry level 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.
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Infographic showing various Entry Level Clinical Programmer Medidata Rave job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 3% As Needed, 78% Full Time, and 18% Part Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Research Coordinator II - Urology

Research Coordinator II - Urology

Baylor College of Medicine

Houston, TX • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Baylor College of Medicine rating

8.6

Company rating: 8.6 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

50th of 532 rated colleges and universities

Job description

Summary

The Scott Department of Urology at Baylor College of Medicine in Houston, TX is seeking a Research Coordinator II to join the growing Bladder Cancer Research Center team. We are looking for an organized and detail‑oriented laboratory professional who will play a key role in supporting the research program.

This position assists with the daily operations of the tissue bank and helps maintain a safe, secure environment for all stored specimens.

Responsibilities include collecting, processing, storing, and transporting human tissue samples across Baylor College of Medicine facilities and affiliated hospitals.

The Coordinator will also support laboratory research projects within the Bladder Cancer Center, including IHC procedures and the collection of tumor, urine, and blood samples for germline analysis and potential longitudinal follow‑up studies.

Job Duties
  • Obtain informed consent, screen, and enroll participants in clinical trials.
  • Manage and maintain study visits, source documentation, adverse events (AEs), serious adverse events (SAEs), concomitant medication logs, as well as study subject and regulatory binders.
  • Process, coordinate, and ship biological specimens (e.g., urine and blood) in accordance with protocol requirements.
  • Coordinate clinical studies in compliance with sponsor protocols and timelines.
  • Collaborate effectively with clinical and non-clinical teams to meet sponsor requirements.
  • Collect, review, and analyze study data; perform accurate EDC data entry.
  • Prepare for and support interim monitoring visits (IMVs), audits, and inspections.
  • Ensure ongoing compliance with IRB and regulatory requirements.
  • Partner with the Research Administration Associate on study renewals with central and local IRBs.
  • Generate quarterly reports on enrollment metrics and study milestones.
  • Work closely with the Principal Investigator (PI) to ensure enrollment targets and protocol compliance are achieved.
  • Develop and implement SOPs aligned with clinical workflows for assigned studies.
  • Establish and maintain systems to track, process, and monitor study activities.
  • Perform other related duties as assigned.
Minimum Qualifications
  • Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
  • One year of relevant experience.
Preferred Qualifications
  • Experience with Pilot and Phase III/IV clinical trials.
  • Familiarity with  electronic medical records system.
  • Experience with EDC systems (e.g., Medidata Rave).
  • Prior regulatory experience.
  • Strong organizational and time management skills.
  • Ability to work independently and collaboratively in a team environment.
  • Knowledge of urology clinical practices and procedures.
  • Some of these studies involve extensive urine sample collection, patient consenting, and retrieval/printing of source documentation from prior urology records.
  • Requires the ability to work collaboratively with multiple providers and coordinate across their clinics.

Work Authorization Requirement:

This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment. 

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

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