Top Tech Jobs & Startup Jobs in Chennai

The Logistics Analyst will analyze logistics data, optimize supply chain processes, collaborate with teams and vendors, and report on performance metrics.

Assist in coordinating clinical trials, maintaining documentation, preparing study materials, and reporting on trial metrics, ensuring compliance.

The RBQM Lead will implement and manage risk-focused quality oversight across clinical studies, collaborating globally with stakeholders to ensure effective risk management throughout the clinical trial lifecycle.

As a Junior Statistical Programmer at ICON plc, you will design and analyze clinical trials, develop programs for data analysis, and assist with regulatory submissions.

The Informed Consent Specialist develops, reviews, and ensures compliance of informed consent forms for clinical trials while collaborating with stakeholders and managing timelines.

Develop and validate R programs for statistical analysis of clinical trial data. Collaborate with biostatisticians, perform QC on outputs, prepare statistical reports for regulatory submissions, and support process improvements. PK and NONMEM expertise required.

Lead implementation, optimization, and maintenance of clinical systems; collaborate with cross-functional teams to define requirements; monitor performance; provide training and stakeholder support to ensure data integrity and regulatory compliance.