ZipRecruiter

Log In

2

Entry Level Clinical Programmer Medidata Rave Jobs

Medidata Solutions

Technical Support Engineer

Iselin, NJ · On-site

$79K - $106K/yr

... Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical ... The Technical Support Engineer is a technical expert who acts as the primary contact between ...

previous pagenext page

Showing results 21-40

All JobsClinical Programmer Medidata Rave JobsEntry Level Clinical Programmer Medidata Rave Jobs

Entry Level Clinical Programmer Medidata Rave information

See salary details

$24

$64

$102

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

As of Aug 11, 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.
More about Entry Level Clinical Programmer Medidata Rave jobs
What cities are hiring for Entry Level Clinical Programmer Medidata Rave jobs? Cities with the most Entry Level Clinical Programmer Medidata Rave job openings:
What are the most commonly searched types of Clinical Programmer Medidata Rave jobs? The most popular types of Clinical Programmer Medidata Rave jobs are:
What job categories do people searching Entry Level Clinical Programmer Medidata Rave jobs look for? The top searched job categories for Entry Level Clinical Programmer Medidata Rave jobs are:
Entry Level Clinical Programmer Medidata Rave jobs near you
Infographic showing various Entry Level Clinical Programmer Medidata Rave job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Data Entry Coordinator

Joint and Muscle Medical Care

Charlotte, NC • On-site

$17/hr

Full-time

Posted 11 days ago

Job description

Clinical Research Data Entry Coordinator — Job Description
Summary

The Clinical Research Data Entry Coordinator supports clinical trials by ensuring timely, accurate, and compliant entry of study data into electronic data capture (EDC) systems. This role works closely with study coordinators, investigators, and monitors to maintain high‑quality documentation and uphold regulatory standards across all assigned studies.
Key Responsibilities
  • Data Entry & Verification — Enter source data into EDC systems (e.g., Medidata Rave, REDCap, Inform) with high accuracy; perform ongoing data cleaning and query resolution.
  • Source Documentation Review — Compare source documents against EDC entries to ensure consistency and completeness.
  • Query Management — Respond to data queries from sponsors/CROs within required timelines; collaborate with clinical staff to obtain missing information.
  • Regulatory Compliance — Maintain adherence to GCP, ICH guidelines, and site SOPs; ensure audit‑ready documentation.
  • Study Support — Assist coordinators with visit documentation, data reconciliation, and tracking of study milestones.
  • Data Quality Assurance — Conduct periodic data reviews, identify trends or recurring issues, and escalate concerns to study leadership.
  • Communication & Collaboration — Work with investigators, coordinators, and monitors to ensure smooth data flow and timely completion of study deliverables.
  • Administrative Tracking — Maintain logs for data entry progress, outstanding queries, and visit completion status.
Required Qualifications
  • Education — Associate’s or Bachelor’s degree in a health‑related field (biology, public health, nursing, etc.).
  • Technical Skills — Experience with EDC platforms; proficiency in Microsoft Excel and basic data management.
  • Attention to Detail — Demonstrated accuracy in data‑heavy environments.
  • Clinical Research Knowledge — Understanding of GCP, ICH, and basic clinical trial workflow.
  • Communication Skills — Ability to collaborate with cross‑functional teams and communicate data needs clearly.
Preferred Qualifications
  • Prior Clinical Research Experience — Experience in a research site, CRO, or academic research setting.
  • Familiarity with Medical Terminology — Ability to interpret clinical notes and lab reports.
  • Experience with Query Resolution — Proven ability to manage sponsor/CRO queries efficiently.
Core Competencies
  • Accuracy & Thoroughness

  • Time Management

  • Confidentiality

  • Problem Solving

  • Process Improvement

Optional Add‑Ons (Depending on Your Use Case)
If you want, I can also generate:
  • A resume bullet list

  • A job posting version

  • A performance evaluation rubric

  • A career progression map

Would you like this rewritten in a more formal HR tone, a shorter version for LinkedIn, or a version tailored to your site’s workflow in Charlotte?