Statistical Programmer (Bangalore,Mumbai,Pune,Home-Based)

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: verdana, geneva;">-Develop and review SAS specifications, programs and output for the creation of ADaM and client defined analysis datasets, tables, listings and graphs in support of statistical Analysis plans.</span><br /><span style="font-family: verdana, geneva;">- Interact with project team members in related discipline e.g. Clinical data management, Clinical Operations and Biostatistics.</span><br /><span style="font-family: verdana, geneva;">- Assume team member responsibilities, including representing Statistical programming at internal project team meetings and with support from statistical programming staff at client meetings.</span><br /><span style="font-family: verdana, geneva;">- Demonstrate good problem solving skills, a proactive approach and a willingness to make decisions, seeking advise from senior Statistical programming staff at client meetings.</span><br /><span style="font-family: verdana, geneva;">- With sufficient experience assume the role of a Lead Programmer for assigned projects.</span><br /><span style="font-family: verdana, geneva;">- Understand scope of project in order to advise Senior statistical programming staff of changes in scope of projects to enable the timely development of change orders.</span><br /><span style="font-family: verdana, geneva;">- Assist with training, mentoring of statistical programmers under the supervision of senior statistical programming staff.</span><br /><span style="font-family: verdana, geneva;">- Participate in statistical programming review of case report forms, annotated CRFs, database structure and study related documentation.</span><br /><span style="font-family: verdana, geneva;">- Review draft and final production runs for projects to ensure quality and consistency.</span><br /><span style="font-family: verdana, geneva;">- Ensure the filing of study documentation is maintained to the standard requirement according to processes and accpetable for audit.</span><br /><span style="font-family: verdana, geneva;">- Prioritize personal workload to meet specified completion dates.</span><br /><span style="font-family: verdana, geneva;">- Carry out all activities according to <span style="font-size: 10pt;">Labcorp Drug Development</span> SOPs working within the framework of the Quality management system and to Good Clinical Pratice (GCP).</span><br /><span style="font-family: verdana, geneva;">- Perform other duties as assigned by Senior Statistical Programming staff.</span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;">Graduate or higher in computing, lifescience, mathematical or Statistical subject</p><p style="margin: 0px;">Alternative academic qualifications or experience are assessed to equivalent background.</p><p style="margin: 0px;"> </p><h2>Experience:</h2><p style="margin: 0px;">-3-5 years experience as Statistical Programmer for amnagement and reporting of clinical trial data.<br />- Demostrated skills in the use of SAS.<br />- Good time management skills and the ability to work to tight deadlines while maintaining the highest standards of work.<br />- Awareness and appreciation of the business needs of a CRO.<br />- Effective communication skills.<br />- Cooperative and team oriented approach.<br />- Self motivation and ability to work independently.</p>