**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...