The electronic Clinical Outcomes Assessment (eCOA) Build Programmer is responsible for designing ... VEEVA EDC and/or RAVE Experience Required:
The electronic Clinical Outcomes Assessment (eCOA) Build Programmer is responsible for designing ... VEEVA EDC and/or RAVE Experience Required:
RAVE, Medidata), Clinical Trial Management Systems required; 3 or more years of experience preferred * Minimum 2 years experience managing multiple projects, meeting deadlines, and adjusting ...
RAVE, Medidata), Clinical Trial Management Systems required; 3 or more years of experience preferred * Minimum 2 years experience managing multiple projects, meeting deadlines, and adjusting ...
Freelance Clinical Programmer Medidata Rave information
What are the key skills and qualifications needed to thrive as a Freelance Clinical Programmer specializing in Medidata Rave, and why are they important?
To excel as a Freelance Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, database design, and programming—often backed by a degree in life sciences, computer science, or a related field. Expertise in Medidata Rave EDC, CDISC standards (SDTM, CDASH), and relevant programming languages like SQL or SAS is typically required, along with certifications in Medidata Rave. Strong attention to detail, problem-solving abilities, and effective communication with cross-functional teams are vital soft skills. These competencies ensure efficient, compliant clinical trial data handling and facilitate seamless collaboration in a highly regulated environment.
What does a Freelance Clinical Programmer specializing in Medidata Rave do?
A Freelance Clinical Programmer with expertise in Medidata Rave is responsible for designing, programming, and maintaining electronic data capture (EDC) systems for clinical trials using the Medidata Rave platform. Their tasks include building and validating study databases, creating eCRFs (electronic Case Report Forms), programming edit checks, and ensuring data integrity and compliance with regulatory standards. As freelancers, they typically work on a contract basis for pharmaceutical companies, CROs, or research organizations, and must stay updated on both industry regulations and the latest Medidata Rave functionalities.
What are some typical challenges a Freelance Clinical Programmer faces when working with Medidata Rave, and how can they be managed?
Freelance Clinical Programmers working with Medidata Rave often encounter challenges such as understanding complex study protocols, handling tight timelines, and ensuring accurate data mapping across multiple studies. Since freelancers may not have immediate access to on-site teams, effective remote communication and documentation are crucial for resolving queries with data managers and sponsors. Staying updated with Medidata Rave's latest features and maintaining strong organizational skills can help manage these challenges efficiently and deliver high-quality results.
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Job description
**Please strictly adhere to the following resume naming convention:
ALL CAPS, NO SPACES B/T UNDERSCORES
Bill Rate market rate - market rate
PTN_US_GBAMSREQID_CANDIDATEBEELINEID
i.e. PTN_US_9999999_SKIPJOHNSON0413
MSP Owner: Zach Provence
Location: Indianapolis, IN
Duration: 6 months
GBaMS ReqID: 10475472
Role Descriptions:
The electronic Clinical Outcomes Assessment (eCOA) Build Programmer is responsible for designing, programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. This role will collaborate with study teams to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.
• Gather and influence eCOA design specifications to enable successful trial implementation
• Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
• Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives
• Partner with Clinical Build Programmer to ensure complete data build for trial data collection needs
• Provide insights into study level deliverables (i.e., Data Management Plan, Project Plan, database, and observed datasets)
• Support submission, inspection and regulatory response activities
• Lead cross Business Unit/Therapeutic Area projects or programs with high complexity
• Handson experience as programmer in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementation
• Design of electronic CRF screens to capture Clinical data and build on required validations
• Understanding of Clinical Protocol and interpretation of the Clinical terminologies to create or design specifications
• Familiarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of system
• Analyse the impact and implement post production changes the Study design
• Data analytics and visualizations
• Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions
• Deciding the technology platform (system/database) for data acquisition and aggregation
Languages Needed:
• Programming experience with HTML, CSS, JAVASCRIPT, Node.js, JSON, SpEL
• • Experience with relational and non-relational database technologies utilizing SQL, Data Functions and Procedures. (e.g., MongoDB)
• Technical proficiency with HTML, Data Mapping, understanding of database structures, etc.
• Experience handling GITLAB utilities
• Quick learner to new trends in technology
• Excellent leadership, communication (written and oral) and interpersonal skills
• Demonstrated leadership in professional setting
• Demonstrated teamwork and collaboration in a professional setting
Desirable Skills:
Keyword:
Skills: VEEVA EDC and/or RAVE
Experience Required:
ALL CAPS, NO SPACES B/T UNDERSCORES
Bill Rate market rate - market rate
PTN_US_GBAMSREQID_CANDIDATEBEELINEID
i.e. PTN_US_9999999_SKIPJOHNSON0413
MSP Owner: Zach Provence
Location: Indianapolis, IN
Duration: 6 months
GBaMS ReqID: 10475472
Role Descriptions:
The electronic Clinical Outcomes Assessment (eCOA) Build Programmer is responsible for designing, programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. This role will collaborate with study teams to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.
• Gather and influence eCOA design specifications to enable successful trial implementation
• Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
• Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives
• Partner with Clinical Build Programmer to ensure complete data build for trial data collection needs
• Provide insights into study level deliverables (i.e., Data Management Plan, Project Plan, database, and observed datasets)
• Support submission, inspection and regulatory response activities
• Lead cross Business Unit/Therapeutic Area projects or programs with high complexity
• Handson experience as programmer in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementation
• Design of electronic CRF screens to capture Clinical data and build on required validations
• Understanding of Clinical Protocol and interpretation of the Clinical terminologies to create or design specifications
• Familiarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of system
• Analyse the impact and implement post production changes the Study design
• Data analytics and visualizations
• Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions
• Deciding the technology platform (system/database) for data acquisition and aggregation
Languages Needed:
• Programming experience with HTML, CSS, JAVASCRIPT, Node.js, JSON, SpEL
• • Experience with relational and non-relational database technologies utilizing SQL, Data Functions and Procedures. (e.g., MongoDB)
• Technical proficiency with HTML, Data Mapping, understanding of database structures, etc.
• Experience handling GITLAB utilities
• Quick learner to new trends in technology
• Excellent leadership, communication (written and oral) and interpersonal skills
• Demonstrated leadership in professional setting
• Demonstrated teamwork and collaboration in a professional setting
Desirable Skills:
Keyword:
Skills: VEEVA EDC and/or RAVE
Experience Required: