Stat Programmer Ii

Updated Yesterday Location Pune MH India Job ID 25104091 Description Stat Programmer II Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical medical affairs and commercial insights into outcomes to address modern market realities Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with but to make us easier to work for Whether you join us in a Functional Service Provider partnership or a Full-Service environment youa ll collaborate with passionate problem solvers innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies because we are passionate to change lives Discover what our 29 000 employees across 110 countries already know WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people through career development and progression supportive and engaged line management technical and therapeutic area training peer recognition and total rewards program We are committed to our Total Self culture a where you can authentically be yourself Our Total Self culture is what unites us globally and we are dedicated to taking care of our people We are continuously building the company we all want to work for and our customers want to work with Why Because when we bring together diversity of thoughts backgrounds cultures and perspectives a wea re able to create a place where everyone feels like they belong Job Responsibilities Job responsibilities a 3-5 Years of Clinical SAS programming Experience a Intermediate to advanced programming skills in R some SAS and or Python experience a bonus a Strong CDISC domain knowledge and implementation a Strong experience with writing and applying Metadata Specifications Derivations a Experience with reuse of various forms of data such as Historical Trial data Real World Data Biomarker data from various sources and Disease Areas a Uses SAS or other software to generate summary tables data listings graphs and derived datasets as specified in the statistical analysis plan and programming specifications a Works to ensure that outputs meet quality standards and project requirements a Performs validation programming and works with other Statistical Programmers Biostatisticians and other project team members to resolve discrepancies or any findings a Keeps project team members informed of programming progress and issues requiring their attention a Follows applicable SOPs WIs and relevant regulatory guidelines e g ICH a Maintains well organized complete and up-to-date project documentation and verification quality control documents and programs ensuring inspection readiness a Manages scheduling and time constraints across multiple projects sets goals based on priorities from management and adapts to timeline or priority changes by reorganizing daily workload a May develop specifications for datasets and outputs according to statistical and Sponsor requirements Anticipates and addresses potential programming issues reflects forethought establishes the basis for efficient programming accurately defines all variables to be accepted by peer review and sponsor requestor with little rework a Prepares in advance for internal meetings contributes ideas and demonstrates respect for opinions of others a Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business a Completes project programming activities within timeframe allotted by Lead Statistical Programmer and or management a May act as the Lead Statistical Programmer directs the programming activities of other programming personnel and monitors progress on programming deliverables a Assists with the transfer of deliverables a Performs other work-related duties as assigned a Minimal travel may be required Qualifications - What wea re looking for a Any graduate Degree preferably in a scientific or statistical discipline In lieu of degree an equivalent combination of education and demonstrated programming experience a Proficiency in programming in SAS or other required software preferably in a clinical trial environment a Excellent written and verbal communication skills a Ability to read write speak and understand English Get to know Syneos Health Over the past 5 years we have worked with 94 of all Novel FDA Approved Drugs 95 of EMA Authorized Products and over 200 Studies across 73 000 Sites and 675 000 Trial patients No matter what your role is youa ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health Additional Information Tasks duties and responsibilities as listed in this job description are not exhaustive The Company at its sole discretion and with no prior notice may assign other tasks duties and job responsibilities Equivalent experience skills and or education will also be considered so qualifications of incumbents may differ from those listed in the The Company at its sole discretion will determine what constitutes as equivalent to the qualifications described above Further nothing contained herein should be construed to create an employment contract Occasionally required skills experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates including the implementation of the EU Equality Directive in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act including the provision of reasonable accommodations when appropriate to assist employees or applicants to perform the essential functions of the job Summary Job responsibilities a 3-5 Years of Clinical SAS programming Experience a Intermediate to advanced programming skills in R some SAS and or Python experience a bonus a Strong CDISC domain knowledge and implementation a Strong experience with writing and applying Metadata Specifications Derivations a Experience with reuse of various forms of data such as Historical Trial data Real World Data Biomarker data from various sources and Disease Areas a Uses SAS or other software to generate summary tables data listings graphs and derived datasets as specified in the statistical analysis plan and programming specifications a Works to ensure that outputs meet quality standards and project requirements a Performs validation programming and works with other Statistical Programmers Biostatisticians and other project team members to resolve discrepancies or any findings a Keeps project team members informed of programming progress and issues requiring their attention a Follows applicable SOPs WIs and relevant regulatory guidelines e g ICH a Maintains well organized complete and up-to-date project documentation and verification quality control documents and programs ensuring inspection readiness a Manages scheduling and time constraints across multiple projects sets goals based on priorities from management and adapts to timeline or priority changes by reorganizing daily workload a May develop specifications for datasets and outputs according to statistical and Sponsor requirements Anticipates and addresses potential programming issues reflects forethought establishes the basis for efficient programming accurately defines all variables to be accepted by peer review and sponsor requestor with little rework a Prepares in advance for internal meetings contributes ideas and demonstrates respect for opinions of others a Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business a Completes project programming activities within timeframe allotted by Lead Statistical Programmer and or management a May act as the Lead Statistical Programmer directs the programming activities of other programming personnel and monitors progress on programming deliverables a Assists with the transfer of deliverables a Performs other work-related duties as assigned a Minimal travel may be required Qualifications - External What wea re looking for a Undergraduate Degree preferably in a scientific or statistical discipline In lieu of degree an equivalent combination of education and demonstrated programming experience a Proficiency in programming in SAS or other required software preferably in a clinical trial environment a Excellent written and verbal communication skills a Ability to read write speak and understand English Share this job