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Mid Level Clinical Programmer Medidata Rave Jobs

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for ... Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

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Mid Level Clinical Programmer Medidata Rave information

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

As of Jun 5, 2026, the average hourly pay for mid 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.
What cities are hiring for Mid Level Clinical Programmer Medidata Rave jobs? Cities with the most Mid 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 states have the most Mid Level Clinical Programmer Medidata Rave jobs? States with the most job openings for Mid Level Clinical Programmer Medidata Rave jobs include:

Clinical Data Specialist 3

DGN Technologies

Mountain View, CA • On-site

Other

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Job description

Description:
 
Responsibilities
Support clinical data review requirements from Lead data manager.
Create customize data review listings for study per specifications from lead data manager
Provide clinical data management support for study operations and analysis groups and lead clinical data manager
Education
BSc/BA/BE or any bachelor degree from relevant field.
Must
Minimum 3-5 years’ experience in data management role
Clinical data review and listing experience (Preferably Medrio, Medidata Rave).
Excellent understanding of data administration and management functions (collection, analysis, data review process, etc.).
Excellent hands on experience on SAS or R programming language for data review listings/tracker
Experience with development of data management trackers and dashboards (Discrepancy listings, Clean patient tracker,
Site trends, study metrics etc.)
Ability of working with multiple teams on multiple projects simultaneously.
Desired
Understand CRF design and interpretation of protocol/CRF requirements to efficient EDC design.
Excellent communication skills
Proficient in MS Office (Excel, PowerPoint, Word, etc.)
Knowledge of Clinical affairs terminology
Knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.

Additional Details

  • Pre-identified worker (First Name, Last Name) & Supplier Name : (No Value)
  • Job Posting Type : Agency Recruited Worker Required
  • Shift : Regular Shift
  • Worker Legal Name (For Manager Sourced Only) : (No Value)