Rammohan Rayicherla Email & Phone Number

Bengaluru, Ka, In

Bengaluru, Karnataka, India

Coordinating with the global teams working on Clinical Trials.Expanding the native team of programmers.

Bengaluru, Karnataka, India

Bengaluru Area, India

Bengaluru Area, India

Bengaluru Area, India

Biostatistical and SAS programming related activities.Provide inputs regarding statistical part in protocol preparation.Prepare Statistical Analysis Plan (SAP) for clinical trial.Prepare the Mock shells according to SAP.Write & validate SAS program to create the table, listing and figure of clinical trial data.Perform the validation of the software used for analysis of statistical data.Write and revise SOP’s as per need and maintain awareness of and adherence to all current SOP’s.Maintain all necessary records for the reporting phase of the study.Validate the SAS program used for generating table, listing and figure.Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements.Mentor team members and conduct performance evaluations.

Bengaluru Area, India

Development & Validation of Efficacy and Safety TFLs.Development & Validation of Case Report Tabulation (CRT) for submission.

Ahmedabad Area, India

Provide inputs regarding statistical part in protocol preparation.Prepare Statistical Analysis Plan (SAP) for clinical trial.Prepare the Mock shells according to SAP.Write & validate SAS program to create the table, listing and figure of clinical trial data.Perform the validation of the software used for analysis of statistical data.Write and revise SOP’s as per need and maintain awareness of and adherence to all current SOP’s.Maintain all necessary records for the reporting phase of the study.Validate the SAS program used for generating table, listing and figure.Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements.Mentor team members and conduct performance evaluations.

Noida Area, India

• Creating tables, figures and listings based on the requirements provided by the Client, by using SAS Drug Development (SDD).• Develop data analysis plans in collaboration with the Client.• Generate macros, listings and tables as part of Statistical analysis in the Clinical Trials Space.• Adherence to industry standards and regulatory requirements, GCP and ICH guideline on Statistical Principles for Clinical Trials• Understand study documents (protocol, CRF, SAP) and explaining them to other colleagues. • Create safety and efficacy TFL• Perform QC checks for TFL • Attend project teleconferences with the customer• Direct Interaction with clients to resolve technical, functional issues• Participate in task forces/initiatives• Mentor new hires to understand methodology and tools used by the team.• Enhance technical skills relevant to statistics and programming

• Providing Statistical Input in Protocol Development• Data verification and management• Analyzing the data as per the protocol and assisting the medical & bio-medical personal in report writing & interpretation of statistical terms. • Providing all types of Statistical help to the research scholars, M.D students and other research associates.

• Providing Statistical Input in Protocol Development• Data verification and management• Analyzing the data as per the protocol and assisting the medical & bio-medical personal in report writing & interpretation of statistical terms. • Providing all types of Statistical help to the research scholars, M.D students and other research associates.

M.Sc, Health Statistics

Ba, Mathematics, Economics And Statistics