Sponsor-dedicated Working fully embedded within one of our pharmaceutical clients with the support of Cytel right behind you you ll be at the heart of our client s innovation As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients a company that is driving the next generation of patient treatment where individuals are empowered to work with autonomy and ownership Position Overview As a Senior Statistical Programmer you will leverage your advanced SAS programming skills to support one or more Phase I-IV clinical trials with a focus on Oncology Our valuesWe believe in applying scientific rigor to reveal the full promise inherent in data We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery We believe in collaboration and invite a diversity of perspectives drawing on a variety of talents to create a wealth of possibilities We prize innovation and seek intelligent solutions using leading-edge technology ShortDescriptionStr Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients At Cytel we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful Cytel is a place where talent experience and integrity come together to advance the state of clinical development Here at Cytel we want our employees to succeed and we enable this success through consistent training development and support To be successful in this position you will have At least 5 years of relevant statistical programming experience in a clinical development setting with 3 years of efficacy preferred BA BSc or higher degree in Statistics Mathematics Computer Science Life Sciences or other related scientific subjects Excellent SAS data manipulation analysis and reporting skills Ability to implement the latest CDISC ADaM standards production validation Solid understanding experience with ADaM efficacy dataset development is required Experience with Oncology is required Experience with submission packages is a plus Working knowledge of latest CDISC SDTM standards Very good oral and written English communication skills InternalQualificationsStr Here at Cytel we want our employees to succeed and we enable this success through consistent training development and support To be successful in this position you will have At least 5 years of relevant statistical programming experience in a clinical development environment with 3 years of efficacy preferred BA BSc or higher degree in Statistics Mathematics Computer Science Life Sciences or other related scientific subjects Excellent SAS data manipulation analysis and reporting skills Ability to implement the latest CDISC ADaM standards production validation Strong understanding experience with ADaM efficacy dataset development is required Experience with Oncology is required Experience with submission packages is a plus Working knowledge of latest CDISC SDTM standards Very good oral and written English communication skills InternalResponsibilitiesStr How you will contribute Performing data manipulation analysis and reporting of clinical trial data on both safety and efficacy utilizing SAS programming Applying CDISC know-how and proficiency to create and validate ADaM datasets analysis files as well as tables listings and figures TLFs Applying your solid understanding experience with safety and efficacy analyses Generating complex ad-hoc reports Preparing and validating submission packages i e define xml Reviewers Guides Pinnacle 21 reports Serving as team player with a willingness to go the extra distance to get results meet deadlines etc Being adaptable and flexible when priorities change ExternalResponsibilitiesStr How you will contribute Performing data manipulation analysis and reporting of clinical trial data on both safety and efficacy utilizing SAS programming Applying CDISC know-how and proficiency to create and validate ADaM datasets analysis files as well as tables listings and figures TLFs Applying your strong understanding experience with safety and efficacy analyses Generating complex ad-hoc reports Preparing and validating submission packages i e define xml Reviewers Guides Pinnacle 21 reports Serving as team player with a willingness to go the extra distance to get results meet deadlines etc Being adaptable and flexible when priorities change

📌 Senior Statistical Programmer Fsp (India)
🏢 Cytel
📍 India