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Position	Statistical Programmer
Work Location	Bangalore
Date Posted	Friday, February 28, 2014

Responsibilities Job Responsibilities: Role is to perform Statistical programming primarily using SAS for reporting and analysis of clinical trials data. Familiarize with GSK environment – complete relevant e-learning and adhere to job specific SOPs and POLs. Maintain a high level of professionalism, performance, productivity and quality. Generate figures, tables and listings Perform Stage 1 and 2 Quality Control (QC) as per GSK QC guidelines. Develop skills for Stage 3 QC. Effectively communicate within team and with customers. Be proactive in Teleconferences Recognize and identify technical problems or data-related issues. Ability to explain routine technical issues with customers (e.g. Clinical, Data management). Familiarity with research relevant literature and regulatory documentation. Ensure proficiency in in-house computer facilities and software. Effectively handle basic multi-task assignments.

Requirements Bachelors or Masters Degree with programming knowledge. 2+ Years of experience in SAS Programming in clinical domain preferably with 1+ years of experience in CDISC High degree of programming and analytical skills. Effective communication skills. Possess solid level of understanding of clinical trial process Strong problem-solving skills. Sound knowledge of SAS and familiarity with other statistical software packages.

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GlaxoSmithKline Consumer Healthcare Ltd. is one of the largest players in the Health Food Drinks industry in India. With a workforce of over 2700 people, a strong marketing and distribution network, and manufacturing plants in Sonepat, Nabha and Rajahmundry, it manufactures Horlicks, Boost, Viva and Maltova, Biscuits and promotes and distributes Eno, Crocin, Iodex, Foodles and other health and nutrition products.
Position	Product Specilist - Oncology
Work Location	Across India
Date Posted	Friday, March 07, 2014

Responsibilities

Requirements Candidate must possess at least a Bachelor of Science , Bachelor of Pharmacy or Master in Business Admin/Post Graduate Diploma in Business Administration/Post Graduate Program in Management in any field. At least 4 year(s) of working experience in the related field is required for this position. Preferably Junior Executives specializing in Sales - Retail/General or equivalent. Job role in Sales Executive or equivalent. 1 Full-Time position(s) available.

Refer This Job To Friends Position Project Data Manager Work Location Bangalore Date Posted Thursday, March 20, 2014 Responsibilities The Portfolio Data Manager is the individual accountable for the Data Management and Programming activities to be delivered for the portfolio level he/she is responsible for. Setting of expectations and overall deliverables at portfolio level Monitoring functional performance via dashboard ROI, KPI review Risk assessment and mitigation plan & compliance management within the project Planning and workload forecasting; review of volume and scope and change in scope if any Setting up of communication plan People management of Lead study data managers reporting into them Internal stakeholder mgt with the project team Interactions with leads of functions and projects in CRO At governance, operational effectiveness of CRO oversight Oversight of the CRO at Project level: Timelines, Resource estimation - long term forecasts (1-3 years), budget set up and invoice review Monitoring of actual vs forecast for budgets Review and approval of TOs and invoices At project level: During the early planning phase, he/she serves as an advisor for Data Management and Programming activities. During the execution phase, he/she manages a team of project data managers, study data managers, data managers, lead-analysts, analysts and programmers working to deliver the different studies in his/her portfolio(s). He/she has to ensure that studies are delivered as mutually agreed with the study teams. After execution, he/she will leverage the learning’s (success or failure) to implement, in his/her area of responsibility, or propose improvements for the future. Requirements 7 to 10 years in Clinical Data Management Experience of all operational aspects of clinical trials from the data management perspective is required to be able to lead a team of various expertises in Data Management and Programming areas. Need to master ICH/GCPs, FDA regulations and other applicable requirements CLICK HERE TO APPLY