Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming ... Experience with EDC systems such as Medidata Rave, Oracle, or Veeva * Working knowledge of CDISC ...
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Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming ... Experience with EDC systems such as Medidata Rave, Oracle, or Veeva * Working knowledge of CDISC ...
... Programming, Medical, and Safety teams on data review strategies and issue resolution Contribute to ... such as Medidata Rave, Oracle, or Veeva Working knowledge of CDISC standards (SDTM/ADaM) and ...
... Programming, Medical, and Safety teams on data review strategies and issue resolution Contribute to ... such as Medidata Rave, Oracle, or Veeva Working knowledge of CDISC standards (SDTM/ADaM) and ...
Remote Medidata Rave Programmer information
What are the main challenges faced by Remote Medidata Rave Programmers, and how can candidates prepare for them?
Remote Medidata Rave Programmers often encounter challenges such as navigating complex study build requirements, ensuring data integrity, and effectively collaborating with cross-functional teams in a virtual environment. Staying organized, maintaining clear communication, and regularly updating stakeholders are essential for success. Familiarity with Medidata Rave’s tools and participating in ongoing training can help you stay current with platform updates and industry standards.
What are the key skills and qualifications needed to thrive as a Remote Medidata Rave Programmer?
To thrive as a Remote Medidata Rave Programmer, you need a solid background in clinical data management, database programming, and a relevant scientific or technical degree. Expertise in Medidata Rave EDC systems, eCRF design, and familiarity with CDISC standards or certifications are typically required. Strong attention to detail, problem-solving ability, and effective remote communication skills set outstanding programmers apart. These competencies ensure accurate, compliant, and efficient clinical trial data capture, which is critical for successful drug development and regulatory submissions.
What is a Remote Medidata Rave Programmer?
A Remote Medidata Rave Programmer is a specialized professional who works from a remote location to design, develop, and maintain electronic data capture (EDC) systems using the Medidata Rave platform. They create and configure study databases, build electronic case report forms (eCRFs), and ensure data integrity in clinical trials. Their work supports the collection, validation, and management of clinical trial data, helping pharmaceutical and biotech companies comply with regulatory requirements. These programmers often collaborate with data managers, clinical teams, and other stakeholders to deliver efficient and accurate solutions.
What are popular job titles related to Remote Medidata Rave Programmer jobs in Connecticut?
For Remote Medidata Rave Programmer jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Remote Medidata Rave Programmer jobs in Connecticut look for?
The top searched job categories for Remote Medidata Rave Programmer jobs in Connecticut are:
What cities in Connecticut are hiring for Remote Medidata Rave Programmer jobs?
Cities in Connecticut with the most Remote Medidata Rave Programmer job openings:
Technical Clinical Data Manager /Data Analyst (Remote)
Fairfield, CT • Remote
Full-time
Posted 16 days ago
Job description
Contact: Neisha Camacho/Terra Parsons -
No 3rd party candidates
We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas.
This role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. The client is seeking someone resourceful and technically curious — not just process-oriented — with the ability to independently explore datasets, generate meaningful reports, and surface potential issues early.
The ideal candidate will bring a blend of traditional clinical data management expertise along with strong data review, querying, and analytical skills. Experience with R, SQL, SAS, or other data interrogation and reporting tools is highly desirable.
Key Responsibilities
- Support clinical data management activities across studies from start-up through database lock
- Perform hands-on data review and exploratory analysis to identify data trends, inconsistencies, missing data patterns, and potential study risks
- Develop custom reports, listings, and data visualizations to support proactive data cleaning and study oversight
- Utilize R, SQL, SAS, or similar tools to query, analyze, and troubleshoot clinical datasets
- Partner with CROs and vendors to ensure high-quality, timely data delivery
- Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams on data review strategies and issue resolution
- Contribute to development and review of key deliverables including:
- Data Management Plans (DMPs)
- eCRF design and completion guidelines
- Edit checks and query logic
- User Acceptance Testing (UAT)
- Data review plans and cleaning processes
- Support ongoing query management and ensure data integrity, consistency, and inspection readiness
- Assist with implementation of data standards, reporting enhancements, and process improvements
- Work independently to investigate data anomalies and recommend practical solutions in a fast-paced biotech environment
Qualifications
- BS in a scientific, technical, or clinical discipline
- Approximately 5–8 years of clinical data management experience within biotech, pharma, or CRO environments
- Strong hands-on experience reviewing and interrogating clinical trial data
- Experience using R, SQL, SAS, or other querying/reporting tools to analyze clinical data and generate custom reports
- Experience with EDC systems such as Medidata Rave, Oracle, or Veeva
- Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage
- Experience supporting Phase II and/or III clinical trials; CNS experience is a plus
- Exposure to CRO/vendor oversight
- Understanding of clinical data structures and dictionaries including MedDRA and WHODrug
- Strong critical thinking and problem-solving skills with the ability to work independently
- Resourceful, proactive, detail-oriented, and comfortable operating in a dynamic biotech environment
- Strong communication and cross-functional collaboration skills
About Penfield Search Partners
Sourced by ZipRecruiter
Industry
Recruiting and staffing services
Company size
11 - 50 Employees
Headquarters location
Fairfield, CT, US
Year founded
2012