... T-SQL programming knowledge. o Should have strong query optimization skills. v Overall ... Clinical Practice regulations and processes is preferable. v Create shared knowledge content and ...
... T-SQL programming knowledge. o Should have strong query optimization skills. v Overall ... Clinical Practice regulations and processes is preferable. v Create shared knowledge content and ...
Clinical Research Coordinator CRC II
Los Angeles, CA · On-site
$26 - $35/hr
Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms * ACRP (CCRC) or SOCRA ... National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA ...
Quick apply
Clinical Research Coordinator CRC II
Los Angeles, CA · On-site
$26 - $35/hr
Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms * ACRP (CCRC) or SOCRA ... National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA ...
Clinical Research Coordinator CRC II
Los Angeles, CA · On-site
$26 - $35/hr
Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms * ACRP (CCRC) or SOCRA ... National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA ...
Quick apply
Clinical Research Coordinator CRC II
Los Angeles, CA · On-site
$26 - $35/hr
Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms * ACRP (CCRC) or SOCRA ... National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA ...
Clinical Research Coordinator CRC II
Los Angeles, CA · On-site
$26 - $35/hr
Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms * ACRP (CCRC) or SOCRA ... National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA ...
Quick apply
Clinical Research Coordinator CRC II
Los Angeles, CA · On-site
$26 - $35/hr
Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms * ACRP (CCRC) or SOCRA ... National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA ...
The Lead Site Clinical Research Coordinator (CRC) is the founding coordinator for Salma Health ... Enter and verify data in electronic data capture (EDC) systems (e.g., REDCap, Medidata Rave) with ...
New
Quick apply
The Lead Site Clinical Research Coordinator (CRC) is the founding coordinator for Salma Health ... Enter and verify data in electronic data capture (EDC) systems (e.g., REDCap, Medidata Rave) with ...
New
LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite day 1
San Francisco, CA · On-site
$109K - $140K/yr
... engineering team. The key responsibility will be to define business rules/logic and provide clear ... Experience with clinical data systems (Medidata RAVE or other EDC platforms). * Familiarity with ...
Quick apply
LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite day 1
San Francisco, CA · On-site
$109K - $140K/yr
... engineering team. The key responsibility will be to define business rules/logic and provide clear ... Experience with clinical data systems (Medidata RAVE or other EDC platforms). * Familiarity with ...
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Quick apply
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Director, Clinical Science
South San Francisco, CA · On-site
$96K - $131K/yr
The Director of Clinical Science will report to the Senior Director of Clinical Development and ... Medidata RAVE. * Experience with natural history studies, epidemiology studies, and real-world ...
Director, Clinical Science
South San Francisco, CA · On-site
$96K - $131K/yr
The Director of Clinical Science will report to the Senior Director of Clinical Development and ... Medidata RAVE. * Experience with natural history studies, epidemiology studies, and real-world ...
Director, Clinical Science
South San Francisco, CA · On-site
$200K - $235K/yr
The Director of Clinical Science will report to the Senior Director of Clinical Development and ... Medidata RAVE. * Experience with natural history studies, epidemiology studies, and real-world ...
Director, Clinical Science
South San Francisco, CA · On-site
$200K - $235K/yr
The Director of Clinical Science will report to the Senior Director of Clinical Development and ... Medidata RAVE. * Experience with natural history studies, epidemiology studies, and real-world ...
Associate Director, Clinical Data Management
Redwood City, CA · On-site
$229K - $269K/yr
The Associate Director, Clinical Data Management ensures optimized data collection, flow and access ... Medidata Rave Coder system * Strong knowledge of the MedDRA and WHODrug dictionaries along with ...
Associate Director, Clinical Data Management
Redwood City, CA · On-site
$229K - $269K/yr
The Associate Director, Clinical Data Management ensures optimized data collection, flow and access ... Medidata Rave Coder system * Strong knowledge of the MedDRA and WHODrug dictionaries along with ...
Proficient knowledge of EDC systems (e.g., Medidata Rave), CDISC standards, and clinical trial processes. * Drive innovation and continuous process improvement within data management by implementing ...
Proficient knowledge of EDC systems (e.g., Medidata Rave), CDISC standards, and clinical trial processes. * Drive innovation and continuous process improvement within data management by implementing ...
Clinical Research Coordinator (Non-RN) - Research & Clinical Management - Genomics (In-Person Role)
San Diego, CA · On-site
$34.14 - $46.94/hr
Any EDC platform such as REDCap, Medidata, Rave) PREFERRED QUALIFICATIONS: Master's Degree 3 Years of Experience Certified Clinical Research Professional (CCRP), Certified Clinical Research ...
Clinical Research Coordinator (Non-RN) - Research & Clinical Management - Genomics (In-Person Role)
San Diego, CA · On-site
$34.14 - $46.94/hr
Any EDC platform such as REDCap, Medidata, Rave) PREFERRED QUALIFICATIONS: Master's Degree 3 Years of Experience Certified Clinical Research Professional (CCRP), Certified Clinical Research ...
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources
San Diego, CA · On-site
$34.14 - $46.94/hr
Any EDC platform such as REDCap, Medidata, Rave) PREFERRED QUALIFICATIONS: Master's Degree 3 Years of Experience Certified Clinical Research Professional (CCRP), Certified Clinical Research ...
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources
San Diego, CA · On-site
$34.14 - $46.94/hr
Any EDC platform such as REDCap, Medidata, Rave) PREFERRED QUALIFICATIONS: Master's Degree 3 Years of Experience Certified Clinical Research Professional (CCRP), Certified Clinical Research ...
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources
San Diego, CA · On-site
$34.14 - $46.94/hr
Any EDC platform such as REDCap, Medidata, Rave) PREFERRED QUALIFICATIONS: Master's Degree 3 Years of Experience Certified Clinical Research Professional (CCRP), Certified Clinical Research ...
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources
San Diego, CA · On-site
$34.14 - $46.94/hr
Any EDC platform such as REDCap, Medidata, Rave) PREFERRED QUALIFICATIONS: Master's Degree 3 Years of Experience Certified Clinical Research Professional (CCRP), Certified Clinical Research ...
Sr. Director, Clinical Science (Autoimmune)
San Diego, CA · On-site
$84K - $115K/yr
More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. * Ability to work ...
Sr. Director, Clinical Science (Autoimmune)
San Diego, CA · On-site
$84K - $115K/yr
More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. * Ability to work ...
Clinical Data Manager
Sunnyvale, CA · On-site
We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery ... EDC system(s) experience (Preferably Medrio and Medidata Rave) Knowledge of Good Clinical Practices ...
Clinical Data Manager
Sunnyvale, CA · On-site
We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery ... EDC system(s) experience (Preferably Medrio and Medidata Rave) Knowledge of Good Clinical Practices ...
Sr. Director, Clinical Data Management
South San Francisco, CA · On-site
$240K/yr
Partner with Clinical Operations, Biostatistics, Statistical Programming, Clinical Science, Medical ... Experience with leading EDC platforms such as Medidata Rave, Veeva EDC, Oracle Clinical, or ...
Sr. Director, Clinical Data Management
South San Francisco, CA · On-site
$240K/yr
Partner with Clinical Operations, Biostatistics, Statistical Programming, Clinical Science, Medical ... Experience with leading EDC platforms such as Medidata Rave, Veeva EDC, Oracle Clinical, or ...
Associate Director, Clinical Science (Autoimmune)
Pasadena, CA · On-site
$170.50 - $208.50/hr
More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. * Ability to work ...
Associate Director, Clinical Science (Autoimmune)
Pasadena, CA · On-site
$170.50 - $208.50/hr
More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. * Ability to work ...
Freelance Clinical Programmer Medidata Rave information
What are the key skills and qualifications needed to thrive as a freelance clinical programmer Medidata Rave?
What does a freelance clinical programmer Medidata Rave do?
What are some typical challenges a freelance clinical programmer Medidata Rave faces when working with Medidata Rave, and how can they be managed?
Full-time
Re-posted 20 days ago
Job description
EROS Technologies was founded with a simple motive of offering the clients exactly what they want, how they want and when they want it. By leveraging for its clients its technological edge and right-sourcing advantage, EROS in a short period of time has grown to become one of the most trusted strategic technology partners. Treating every client as the top priority, we customize our solutions and services to align with the unique needs of each client.
Position: - Rave Medidata Support Analyst
Location: - San Francisco, CA
Joining Mode: - Full Time
Job Description:-
v Perform root cause analysis: - Identify the technical root cause of an incident. Identify resolution and technical fix required. Identify and document workarounds as necessary.
o Familiar with Rave EDC & Architect (study build) functionality.
o Should be proficient with C# coding.
o Should have strong JAVA knowledge.
o Should have strong Oracle SQL knowledge.
o Should have strong T-SQL programming knowledge.
o Should have strong query optimization skills.
v Overall understanding of the Software Development Life Cycle and familiarity with Good Clinical Practice regulations and processes is preferable.
v Create shared knowledge content and maintain knowledge base: - Create new knowledge content useful for all future resources according to knowledge documentation requirements. Continually maintain tip sheets, frequently asked questions, common issue responses, and all applicable knowledge documents to ensure accuracy and completeness.
v Ownership of issues assigned: - Drive resolution for all assigned issues, tasks, or incidents.
v Technical issue communication: - Provide technical details, impact assessments, and test case details to SQA resources for changes.
v Work cross functionally to resolve issues: - Work across IT teams if issues are related to Databases, Network, Firewall, Cyclone, Sterling, etc.
v Document impact assessment Provide impact assessment of Rave changes to the integrations.
v Adhoc queries: - Create and run adhoc queries as requested by RAVE teams or customers.
v Monitor integration jobs: - Ensure the integration jobs run according to schedule. Escalate or resolve issues as required.
v Reconciliation reports: - Develop and run reconciliation scripts and reports.
v Issue / bug impact assessment: - Develop and execute scripts to identify how studies (and users) are impacted by bugs. Develop reports and analysis to show the impact.
v Develop workarounds: - Develop workarounds and Knowledge objects for L3 support if bugs are identified that will not be resolved immediately.
v Change control process technical support: - Provide technical details for and follow the approved Client Change Control process. This includes support of validation activities.
v Maintain design documentation: - Update and maintain design documentation with every bug fix, release, or change.
v Unit testing: - Perform Unit testing for bug fixes.
v Incident resolution: - Provide clear and understandable directions / resolutions that are acceptable to the customer and resolve the incident.
v Enhancement Development: - Develop and deploy enhancement code per the Client requirements for the custom, in-house integrations. Work with Client SQA testers to ensure code is production ready. Follow the Client approved change control process to deploy code.
v Bug Fix Development: - Develop and deploy bug fix code independently, as required for the custom, in-house integrations. Work with Client SQA testers to ensure code is production ready. Follow the Client approved change control process to deploy code.
v Maintain Custom Integrations: - Maintain code for custom, in-house integrations.
All your information will be kept confidential according to EEO guidelines.
About Eros Technologies
Sourced by ZipRecruiter
We create a culture that inspires us to work smart, together. Experience Eros is dedicated to delivering services to all our Fortune 100 to Fortune 500, SME, and Enterprise customers in the USA, Canada, and India. Eros Technologies is a leading Global Consulting and IT services company, offering a wider variety of solutions customized to the needs of demanding industries and diversified business environments. We help clients move forward in every part of their businesses, from strategic planning to day-to-day operations by enhancing our consulting and outsourcing expertise with alliances and other capabilities. Eros can mobilize the right people, skills, and technologies to help its clients improve their performances. We create Solutions with the aim of increasing your organization’s efficiency, productivity, and profits.
Industry
Human resources consulting services
Company size
1,001 - 5,000 Employees
Headquarters location
Lewes, DE, US
Year founded
2015