Top Tech Jobs & Startup Jobs in Mumbai

The TMF Document Assistant performs quality control of study documents, identifies quality issues, updates metadata in the eTMF system, and participates in training.

Lead programming activities for clinical trials, develop SAS code for statistical analysis, ensure quality outputs, manage multiple projects, and mentor programming personnel.

The Safety and PV Ops Specialist II maintains compliance with safety regulations, supports quality assurance activities, and manages safety database operations while ensuring training and proposal support for the Pharmacovigilance team.

The Principal Biostatistician mentors staff, oversees biostatistical work, develops training, prepares analysis plans, and ensures quality in statistical deliverables for clinical projects.

The Sr. Statistical Programmer develops programming code using SAS to generate statistical outputs, ensures quality standards, manages multiple projects, and leads programming teams. Responsibilities include documentation, communication with teams, and mentoring programming personnel while participating in sponsor meetings.

The Safety & PV Specialist I is responsible for data entry and tracking of safety reports, maintaining compliance with SOPs, and conducting literature reviews related to safety in clinical trials.

The Sr Statistical Programmer develops custom programming code using SAS to create statistical outputs, ensures quality standards, and manages programming documentation and team coordination while acting as a lead for programming tasks.

The role involves developing custom SAS programs for clinical data analysis, ensuring quality standards, collaborating with project teams, and mentoring junior programmers.

The Senior Clinical Programmer is responsible for programming, testing database designs, managing reporting tools, troubleshooting issues, and collaborating with teams to ensure compliance and data integrity in clinical programming tasks.

The Principal Biostatistician in Clinical Pharmacology will lead statistical aspects of clinical studies, contribute to research design, and collaborate with teams to ensure drug development success.