Opportunity Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
We are seeking a highly skilled **DM/Safety Review/Medical Review/Central Monitoring Programmer with expertise in TIBCO Spotfire and JReview (J-Review),** along with strong clinical domain knowledge, to design, develop, and support interactive dashboards for clinical data review and safety monitoring. The role involves close collaboration with cross-functional teams to deliver high-quality, compliant, and insight-driven visualizations for clinical decision-making.
**Key Responsibilities**
+ Design, develop, and maintain complex **Spotfire, JReview, allied analytics tool dash...
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
We are seeking a highly skilled **DM/Safety Review/Medical Review/Central Monitoring Programmer with expertise in TIBCO Spotfire and JReview (J-Review),** along with strong clinical domain knowledge, to design, develop, and support interactive dashboards for clinical data review and safety monitoring. The role involves close collaboration with cross-functional teams to deliver high-quality, compliant, and insight-driven visualizations for clinical decision-making.
**Key Responsibilities**
+ Design, develop, and maintain complex **Spotfire, JReview, allied analytics tool dash...
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