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 ...
We use Objective C and Swift programming languages to create native applications for iPhone ... Medidata RAVE system Additional Information Webcam Interview is acceptable.
We use Objective C and Swift programming languages to create native applications for iPhone ... Medidata RAVE system Additional Information Webcam Interview is acceptable.
Medidata RAVE system Lead Clinical Research Associate duties: * Under supervision of Clinical Project Lead, oversees performance of assigned field monitors and site activities in accordance with the ...
Medidata RAVE system Lead Clinical Research Associate duties: * Under supervision of Clinical Project Lead, oversees performance of assigned field monitors and site activities in accordance with the ...
Clinical Data Manager
Sunnyvale, CA · On-site
$70 - $75/hr
Clinical data review and listing experience (Preferably Medrio, Medidata Rave). * Excellent ... Excellent hands on experience on SAS or R programming language for data review listings/tracker.
Quick apply
Clinical Data Manager
Sunnyvale, CA · On-site
$70 - $75/hr
Clinical data review and listing experience (Preferably Medrio, Medidata Rave). * Excellent ... Excellent hands on experience on SAS or R programming language for data review listings/tracker.
Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ... Communication and escalation of project level issues including processes, timelines, resourcing ...
Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ... Communication and escalation of project level issues including processes, timelines, resourcing ...
Review incoming clinical data for completeness, consistency, and accuracy. Generate, track, and ... Experience with EDC systems (e.g., Medidata Rave, Veeva Vault, Medrio) a plus.
Review incoming clinical data for completeness, consistency, and accuracy. Generate, track, and ... Experience with EDC systems (e.g., Medidata Rave, Veeva Vault, Medrio) a plus.
Clinical Data Manager
Austin, TX · On-site
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong ... Experience with data listings, query management, edit check programming, and coding dictionaries (e ...
Clinical Data Manager
Austin, TX · On-site
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong ... Experience with data listings, query management, edit check programming, and coding dictionaries (e ...
Senior Data Validator, Clinical Oversight & Standards
King Of Prussia, PA · Hybrid
$143K - $169K/yr
This role reports to the Director, Statistical Programming Lead Work Environment: *** On site ... Proficiency with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design ...
Senior Data Validator, Clinical Oversight & Standards
King Of Prussia, PA · Hybrid
$143K - $169K/yr
This role reports to the Director, Statistical Programming Lead Work Environment: *** On site ... Proficiency with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design ...
OR · On-site
Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ... Communication and escalation of project level issues including processes, timelines, resourcing ...
OR · On-site
Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ... Communication and escalation of project level issues including processes, timelines, resourcing ...
Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python * Proven experience in clinical trial programming and database management * Knowledge ...
Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python * Proven experience in clinical trial programming and database management * Knowledge ...
Infrastructure & Middleware Engineer
Iselin, NJ · On-site
$101K - $135K/yr
... Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical ... Mid-Level Autonomy: You can independently scope and execute infrastructure projects (e.g., "Migrate ...
Infrastructure & Middleware Engineer
Iselin, NJ · On-site
$101K - $135K/yr
... Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical ... Mid-Level Autonomy: You can independently scope and execute infrastructure projects (e.g., "Migrate ...
Clinical Data Manager
Aliso Viejo, CA · On-site
$45 - $48/hr
Medidata RAVE * Oracle Inform * Medidata * Similar EDC systems * Experience with database concepts ... Experience with SQL, SAS, Excel, or programming tools is a plus * BS degree or higher in Biological ...
New
Clinical Data Manager
Aliso Viejo, CA · On-site
$45 - $48/hr
Medidata RAVE * Oracle Inform * Medidata * Similar EDC systems * Experience with database concepts ... Experience with SQL, SAS, Excel, or programming tools is a plus * BS degree or higher in Biological ...
New
... of mid to late-stage CKD studies. This role partners closely with cross-functional teams and ... Experience with clinical systems (e.g., Medidata Rave, Veeva) * Experience with study start-up ...
... of mid to late-stage CKD studies. This role partners closely with cross-functional teams and ... Experience with clinical systems (e.g., Medidata Rave, Veeva) * Experience with study start-up ...
Drug Discovery Specialist - Fully Remote | Upto $1450 Part-time
San Francisco, CA · Remote
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
Quick apply
Drug Discovery Specialist - Fully Remote | Upto $1450 Part-time
San Francisco, CA · Remote
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
Pharmaceutical Research PhD - Expert
San Francisco, CA · On-site +1
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
Quick apply
Pharmaceutical Research PhD - Expert
San Francisco, CA · On-site +1
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
Research Database Developer
Cincinnati, OH · On-site
$90K - $120K/yr
Implement and manage electronic data capture (EDC) systems such as Medidata Rave * Develop, design ... Apply knowledge of clinical research methods to support various clinical trials and research ...
Research Database Developer
Cincinnati, OH · On-site
$90K - $120K/yr
Implement and manage electronic data capture (EDC) systems such as Medidata Rave * Develop, design ... Apply knowledge of clinical research methods to support various clinical trials and research ...
Research Database Developer
Cincinnati, OH · Remote
$90K - $120K/yr
... within clinical research settings. The ideal candidate will possess proficiency in programming ... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ...
Research Database Developer
Cincinnati, OH · Remote
$90K - $120K/yr
... within clinical research settings. The ideal candidate will possess proficiency in programming ... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ...
In this position, you will contribute to mid- to late-stage clinical studies, working cross ... Experience working with clinical trial systems such as Medidata Rave, Veeva, or similar platforms.
In this position, you will contribute to mid- to late-stage clinical studies, working cross ... Experience working with clinical trial systems such as Medidata Rave, Veeva, or similar platforms.
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
Director, Clinical Data Management
New York, NY · On-site
$220K - $250K/yr
Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures ... Provide proactive input into clinical protocol design to ensure data collection strategies align ...
Director, Clinical Data Management
New York, NY · On-site
$220K - $250K/yr
Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures ... Provide proactive input into clinical protocol design to ensure data collection strategies align ...
Mid Level Clinical Programmer Medidata Rave information
See salary details
$24.76 - $31.84
3% of jobs
$31.84 - $38.92
4% of jobs
$38.92 - $46
9% of jobs
$46 - $53.08
5% of jobs
$54.30 is the 25th percentile. Wages below this are outliers.
$53.08 - $60.16
17% of jobs
The median wage is $63.26 / hr.
$60.16 - $67.24
25% of jobs
$71.78 is the 75th percentile. Wages above this are outliers.
$67.24 - $74.32
17% of jobs
$74.32 - $81.40
9% of jobs
$81.40 - $88.48
6% of jobs
$88.48 - $95.56
2% of jobs
$95.56 - $102.64
1% of jobs
$24
$64
$102
How much do mid level clinical programmer medidata rave jobs pay per hour?
Job description
We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. 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 requires a solid understanding of clinical trials, data integration, and programming techniques to support the creation, validation, and execution of clinical study data in a fast-paced environment.
Key Responsibilities:
- Programming and Development: Write and maintain code for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment.
- Data Management and Quality: Ensure accurate and timely delivery of clinical trial data by performing data checks, validation, testing, and reconciliation in line with clinical trial timelines and regulatory requirements.
- Collaboration: Work closely with clinical data managers, statisticians, and other stakeholders to design and implement clinical data flow, ensuring compliance with all regulatory requirements.
- Troubleshooting and Issue Resolution: Identify, investigate, and resolve any issues that arise within the platform or clinical data programming processes.
- Documentation: Maintain comprehensive documentation of programming processes, code, and data management workflows for audit and regulatory purposes.
- Continuous Improvement: Contribute to the improvement of programming practices, tools, and templates to streamline clinical programming workflows and enhance efficiency.
- Training and Mentorship: Provide guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating knowledge sharing within the team.
- Experience: 4-6 years of experience in clinical programming.
- Technical Skills:
- Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.).
- Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and programming solutions.
- Strong knowledge of clinical trial data structures, data standards (e.g., CDISC, SDTM), and regulatory requirements (e.g., FDA, EMEA).
- Problem-Solving: Excellent troubleshooting and problem-solving skills with the ability to work under pressure to meet deadlines.
- Communication: Strong communication skills with the ability to collaborate effectively with cross-functional teams and communicate technical concepts to non-technical stakeholders.
- Education: Bachelor's degree or higher in Computer Science, Life Sciences, Engineering, or related field (or equivalent work experience).
Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.