Exciting Opportunity for a CDM Programmer (Spotfire) II – Work from Home in India!
Are you passionate about clinical data analysis and visualization We are seeking a talented CDM Programmer (Spotfire) II to join our dynamic team remotely from India. This role offers a unique chance to leverage your expertise in Spotfire, JReview, and clinical data management to support critical drug development processes. If you thrive in a collaborative environment and are eager to expand your skills in data wrangling, dashboard development, and regulatory-compliant visualization, this is the perfect opportunity for you to make an impact in the clinical research space.
Required Skills
- Proven experience with TIBCO Spotfire and JReview (J-Review) for clinical data visualization
- Strong programming skills in IronPython, Python, HTML, and scripting for dashboard enhancement
- Robust understanding of clinical data domains such as SDTM, AE/SAE, and MedDRA coding
- Data wrangling and transformation expertise using Spotfire Data Canvas, Python, and other tools
- Knowledge of clinical data standards, GxP regulations, and regulatory compliance
- Experience with data integration from multiple sources like EDC (Veeva), CTMS, and safety databases
- Analytical skills to develop automated QC, validation, and reporting solutions
- Excellent troubleshooting, problem-solving, and performance tuning abilities
- Strong stakeholder communication skills and ability to collaborate cross-functionally
Nice To Have Skills
- Familiarity with other analytics tools like SAS, Crystal Reports, or relational RDBMS
- Experience with clinical operational metrics and drug development lifecycle phases
- Knowledge of GCP guidelines and regulatory documentation practices
- Ability to learn new data analytics tools and adapt to evolving project needs
Preferred Education And Experience
- Bachelor's degree or higher in life sciences, computer science, or related field
- 4+ years of experience in clinical data management, programming, or visualization roles
- Prior exposure to clinical trial data, safety monitoring, and medical review processes
Other Requirements
- Open to working independently on a remote basis within India
- Willingness to learn and adapt to new tools and technologies as required
- Ability to meet project deadlines and manage multiple priorities effectively
Take your clinical data expertise to the next level—apply now to join a forward-thinking team dedicated to advancing healthcare through innovative data solutions!
