Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating ...
Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating ...
CDM Programmer II - Medidata Rave Location: Wilmington, NC , United States Description : Note: Skill set required is RAVE, edit check expertise/customs function programming. BELT experience, protocol ...
CDM Programmer II - Medidata Rave Location: Wilmington, NC , United States Description : Note: Skill set required is RAVE, edit check expertise/customs function programming. BELT experience, protocol ...
Clinical Development Engineer (Medidata Rave / Technical Support) We are seeking a Clinical Development Support Engineer with deep technical expertise in Medidata Rave and related clinical data ...
Clinical Development Engineer (Medidata Rave / Technical Support) We are seeking a Clinical Development Support Engineer with deep technical expertise in Medidata Rave and related clinical data ...
EDC Programmer
Redmond, WA · On-site
$100K - $150K/yr
Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration. * Develop custom ...
Quick apply
EDC Programmer
Redmond, WA · On-site
$100K - $150K/yr
Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration. * Develop custom ...
Build and configure study databases in Medidata Rave or other eClinical platforms based on protocol ... Edit Check Programming and Validation * Develop and maintain edit checks, derivations, dynamics ...
New
Build and configure study databases in Medidata Rave or other eClinical platforms based on protocol ... Edit Check Programming and Validation * Develop and maintain edit checks, derivations, dynamics ...
New
EDC Programmer
Redmond, WA · On-site
$100K - $150K/yr
Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration. * Develop custom ...
EDC Programmer
Redmond, WA · On-site
$100K - $150K/yr
Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration. * Develop custom ...
RAVE Medidata -Onsite
Minneapolis, MN · On-site
RAVE Medidata -Onsite Location: Minneapolis MN Duration: Fulltime Client : TCS e Relevant Experience (in Yrs)6+ Technical/Functional Skills • Hands on Experience on RAVE - Medidata • Experience ...
RAVE Medidata -Onsite
Minneapolis, MN · On-site
RAVE Medidata -Onsite Location: Minneapolis MN Duration: Fulltime Client : TCS e Relevant Experience (in Yrs)6+ Technical/Functional Skills • Hands on Experience on RAVE - Medidata • Experience ...
RAVE Medidata -Onsite Location: Minneapolis MN Duration: Fulltime Client : TCS e Relevant Experience (in Yrs) 6+ Technical/Functional Skills Hands on Experience on RAVE - Medidata Experience on ...
RAVE Medidata -Onsite Location: Minneapolis MN Duration: Fulltime Client : TCS e Relevant Experience (in Yrs) 6+ Technical/Functional Skills Hands on Experience on RAVE - Medidata Experience on ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Sr Manager Standards & Systems
Plainsboro, NJ · On-site
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Sr Manager Standards & Systems
Plainsboro, NJ · On-site
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Clinical Research Nurse
Philadelphia, PA · Hybrid
$40 - $45/hr
... citi, medidata rave, sae, adverse event, Oncology, Gcp, Clinical research, Chart review, Pre ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Quick apply
Clinical Research Nurse
Philadelphia, PA · Hybrid
$40 - $45/hr
... citi, medidata rave, sae, adverse event, Oncology, Gcp, Clinical research, Chart review, Pre ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows. * Strong Excel VBA programming skills, with proven experience in data validation and reconciliation. * Deep ...
Position: - Rave Medidata Support Analyst Location: - San Francisco, CA Joining Mode: - Full Time - ... T-SQL programming knowledge. o Should have strong query optimization skills. v Overall ...
Position: - Rave Medidata Support Analyst Location: - San Francisco, CA Joining Mode: - Full Time - ... T-SQL programming knowledge. o Should have strong query optimization skills. v Overall ...
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards Governance experience (CDISC) REQUIRED Candidates whose resumes do not clearly demonstrate Medidata ...
New
Trainee Medidata Rave Programmer information
See salary details
$12.02 - $17.18
4% of jobs
$17.18 - $22.33
9% of jobs
$26.04 is the 25th percentile. Wages below this are outliers.
$22.33 - $27.49
17% of jobs
$27.49 - $32.65
13% of jobs
The median wage is $35.66 / hr.
$32.65 - $37.81
13% of jobs
$37.81 - $42.96
10% of jobs
$42.96 - $48.12
9% of jobs
$49.09 is the 75th percentile. Wages above this are outliers.
$48.12 - $53.28
9% of jobs
$53.28 - $58.44
7% of jobs
$58.44 - $63.59
6% of jobs
$63.59 - $68.75
4% of jobs
$12
$39
$68
How much do trainee medidata rave programmer jobs pay per hour?
As of Jul 11, 2026, the average hourly pay for trainee 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 the difference between Trainee Medidata Rave Programmer vs Junior Clinical Data Coordinator?
| Aspect | Trainee Medidata Rave Programmer | Junior Clinical Data Coordinator |
|---|---|---|
| Required Credentials | Basic knowledge of Medidata Rave, relevant coursework or certifications | Degree in life sciences or related field, some data management training |
| Work Environment | Clinical trial data management teams, often in CROs or pharma companies | Clinical trial sites or data management departments within pharma |
| Industry Usage | Primarily in clinical data management and EDC system setup | Data collection, validation, and quality control in clinical trials |
The Trainee Medidata Rave Programmer focuses on learning and supporting EDC system setup and data entry using Medidata Rave, while the Junior Clinical Data Coordinator handles data validation and management at clinical sites. Both roles require familiarity with clinical data processes but differ in responsibilities and focus areas.
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Contractor
Re-posted 20 days ago
Job description
Sr Medidata RAVE Programmer
Remote from anywhere in the U.S. or Canada
Contract/Corp to Corp
JOB OVERVIEW
The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and provides EDC programming support to the study team in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice (GCP), ICH Guidelines and sponsor requirements. The EDC Programmer also assists in technical support for data collection systems.
JOB RESPONSIBILITIES
• Perform study set up and program edit check programming as per the approved specifications with minimal guidance from the line manager or experienced colleagues
• Adhere to project timelines
• Participate in the design and maintenance of the clinical study database per the protocol and any amendments, SOPs, GCP and other regulatory requirements
• Review database specifications and Data Validation Specifications (DVS) and perform programming and configuration activities
• Assist in database release to production activities
• Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position. Assist data manager with status reports and listings as necessary
• Advise management on a regular basis on the status and any potential risks or concerns with ongoing projects to ensure timely resolution including any potential issues with resources
• Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated, and understood
• Participate in internal and external study team meetings, as required
• Participate in department meetings and initiatives
• Perform other duties as required by the department
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
• 2-4years EDC Programming experience working in pharmaceutical, biotechnology or Contract Research Organization (CRO) preferred
• Course completion of an EDC system training
• Minimum 2-4 years of experience in clinical database design and deployment
• Additional relevant work experience will be considered in lieu of formal qualifications
• Broad knowledge of drug development processes
• Understanding of global clinical development budgets and relationship to productivity targets
• Knowledge of effective clinical data management practices
PREFERRED SKILLS
• Good organizational skills
• Good communication skills, verbal and written
• Detail oriented
• Good computer skills, including Microsoft Office and use of data management systems
• Good problem-solving skills
• Basic knowledge and understanding of EDC and other eTechnologies
• Flexible, team player
• Proven ability to organize and effectively prioritize workload and deliverables
Remote from anywhere in the U.S. or Canada
Contract/Corp to Corp
JOB OVERVIEW
The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and provides EDC programming support to the study team in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice (GCP), ICH Guidelines and sponsor requirements. The EDC Programmer also assists in technical support for data collection systems.
JOB RESPONSIBILITIES
• Perform study set up and program edit check programming as per the approved specifications with minimal guidance from the line manager or experienced colleagues
• Adhere to project timelines
• Participate in the design and maintenance of the clinical study database per the protocol and any amendments, SOPs, GCP and other regulatory requirements
• Review database specifications and Data Validation Specifications (DVS) and perform programming and configuration activities
• Assist in database release to production activities
• Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position. Assist data manager with status reports and listings as necessary
• Advise management on a regular basis on the status and any potential risks or concerns with ongoing projects to ensure timely resolution including any potential issues with resources
• Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated, and understood
• Participate in internal and external study team meetings, as required
• Participate in department meetings and initiatives
• Perform other duties as required by the department
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
• 2-4years EDC Programming experience working in pharmaceutical, biotechnology or Contract Research Organization (CRO) preferred
• Course completion of an EDC system training
• Minimum 2-4 years of experience in clinical database design and deployment
• Additional relevant work experience will be considered in lieu of formal qualifications
• Broad knowledge of drug development processes
• Understanding of global clinical development budgets and relationship to productivity targets
• Knowledge of effective clinical data management practices
PREFERRED SKILLS
• Good organizational skills
• Good communication skills, verbal and written
• Detail oriented
• Good computer skills, including Microsoft Office and use of data management systems
• Good problem-solving skills
• Basic knowledge and understanding of EDC and other eTechnologies
• Flexible, team player
• Proven ability to organize and effectively prioritize workload and deliverables