The key responsibilities of the positions will include : - Leads activities to identify new business opportunities for Statistical services - Preparation and review of Statistical Analysis Plans and Statistical Contributions, with appropriate guidance from other statistical staff. - Statistical analysis of clinical trial data using basic methodology, with appropriate guidance from other statistical staff. - Production of data tables and graphs to the required specification for clinical, pharmacokinetic and statistics reports. - Preparation of randomization specifications and the generation of randomization schedules. - Perform sample size calculations as required. - Provide statistical support to SAS Programmers. - SAS programming and related activities for the presentation and analysis of clinical trial data. - Review of protocols, providing a statistical advice service for internal and external clients. - Scheduling of clinical statistical work to meet required deadlines. Ensuring that projects are completed in a timely and accurate manner. - Liaison with internal and external clients, as required, with regards to the requirements for analysis, tables and graphs. - Review of Clinical Study Reports. - Perform peer review of other Statisticians- work. - Perform Quality Control of analysis data sets, data displays for secondary efficacy and safety variables. - Training of other members of staff within the department in statistical methods and programming techniques. - Assist Business Development in forecasting Statistic resource needs for new Requirement : - Masters, or higher qualifications in Statistics - Minimum 10-12 years- experience as a Statistician in CRO or Pharma - Excellent working knowledge of SAS software - Working knowledge of relevant "Data Standards (such as CDISC / ADaM) is a must." - Experience managing projects. - Experience in team coordination. - Working knowledge of regulatory requirements for clinical trials and medical research. - Strong focus on quality and timely delivery of work. - Well organized with good time management skills. - Strong problem solving and analytical skills. - Excellent interpersonal skills with a high level of proficiency in English - Ability to work well and flexibly i.e. autonomously, in small teams and with a wide range of varying stakeholders. - Ability to see the big picture, whilst still maintaining a focus on detail and implementation - Strong leadership and mentoring skills Interested applicants anywhere in Bangalore can write to or call Sneha @ 8310560030

Bangalore

Principal Programmer - Bio Statistics - Clinical Research - Pharma 

Principal Programmer - Bio Statistics - Clinical Research - Pharma  ,Job Description for Principal Programmer - Bio Statistics - Clinical Research - Pharma  in HeadPro Consulting LLP in  Bangalore for (10-12) years of experience. Apply Now!

Job Description for Principal Programmer - Bio Statistics - Clinical Research - Pharma  in HeadPro Consulting LLP in  Bangalore for (10-12) years of experience. Apply Now!