Thank you for showing interest to join our multi-talented and fast-growing teams. Currently we are actively hiring for multiple positions, and we are looking for professional individuals with leadership and organizational skills.
We strongly believe our strength is our people, and we are highly committed to professional development of our employees. Culture and values driven workplace, flexible working conditions, talent recognition, knowledge sharing, and learning are some of the instincts of Clinytica.
NJ, USA
Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs).Looking for well experienced candidates with strong motive to thrive in analytics in pharma industry. This position is ideal for the people who are looking for career promotions.
Job Descriptionprogramming support in one or more Phase I-III clinical studies. Programming on SDTM and ADaM datasets, including production and validation. Programing tables, listings, figures (TFL), including production and validation. Create SDTM and Adam specifications, or review specifications and provide comments. Prepare e-sub packages for regulatory submissions. Work on ad-hoc requests, medical marketing access presentations, manuscripts and any other requests. Architect and execute utility macros to increase programing efficiency. Mentor junior programmers and guide them with company and client standards. Act as lead programmer for assigned projects, and take responsibility for all programing activities of the study. Foresee the deliverable, commitments and their associated risks, communicate with resourcing manager periodically.
ResponsibilitiesBachelor’s degree in Statistics, Biostatistics Mathematics or other science related degree. 5+ years of experience in SAS programing in clinical industry. Complete understanding of clinical trial study designs and statistical analysis. 3+ years of working experience on CDISC standards. Experience in regulatory submission process in at least one clinical trial study. Certification in Base SAS, Clinical SAS and Advanced SAS. Excellent communication and interpersonal skills to effectively interact with others. Team lead experience is added weight.
HYDERABAD, INDIA
Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs).Looking for well experienced candidates with strong motive to thrive in analytics in pharma industry. This position is ideal for the people who are looking for career promotions.
Job Descriptionprogramming support in one or more Phase I-III clinical studies. Programming on SDTM and ADaM datasets, including production and validation. Programing tables, listings, figures (TFL), including production and validation. Create SDTM and Adam specifications, or review specifications and provide comments. Prepare e-sub packages for regulatory submissions. Work on ad-hoc requests, medical marketing access presentations, manuscripts and any other requests. Architect and execute utility macros to increase programing efficiency. Mentor junior programmers and guide them with company and client standards. Act as lead programmer for assigned projects, and take responsibility for all programing activities of the study. Foresee the deliverable, commitments and their associated risks, communicate with resourcing manager periodically.
ResponsibilitiesBachelor’s degree in Statistics, Biostatistics Mathematics or other science related degree. 5+ years of experience in SAS programing in clinical industry. Complete understanding of clinical trial study designs and statistical analysis. 3+ years of working experience on CDISC standards. Experience in regulatory submission process in at least one clinical trial study. Certification in Base SAS, Clinical SAS and Advanced SAS. Excellent communication and interpersonal skills to effectively interact with others. Team lead experience is added weight.
HYDERABAD, INDIA
Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs). Looking for well experienced candidates with strong motive to thrive in analytics in pharma industry.
Job Descriptionprogramming support in one or more Phase I-III clinical studies. Programming on SDTM and ADaM datasets, including production and validation. Programing tables, listings, figures (TFL), including production and validation. Create SDTM and Adam specifications, or review specifications and provide comments. Work on ad-hoc requests, medical marketing access presentations, manuscripts and any other requests. Assist in the creation of utility macros to increase programing efficiency. Foresee the deliverable, commitments and their associated risks, communicate with line manager periodically.
ResponsibilitiesBachelor’s degree in Statistics, Biostatistics Mathematics or other science related degree. 2+ years of experience in SAS programing in clinical industry. Good understanding of clinical trial study designs and statistical analysis. 1+ years of working experience on CDISC standards. Experience in regulatory submission process will be appreciated. Certification in Base SAS, Clinical SAS and Advanced SAS. Excellent communication and interpersonal skills to effectively interact with others.
HYDERABAD, INDIA
Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs). Looking for well experienced candidates with strong motive to thrive in analytics in pharma industry. This position is ideal for the people who are looking for career promotions.
Job Descriptionprogramming support in one or more Phase I-III clinical studies. Programing on SDTM and ADaM datasets Programing tables, listings, figures (TFL)
ResponsibilitiesBachelor’s degree in Statistics, Biostatistics Mathematics or other science related degree. Familiarity of SAS coding, including Base SAS, SQL and Macros. Certification in Clinical and Advanced is added weight. Base SAS certification Basic knowledge on clinical trial studies design. Certification in Base SAS, Clinical SAS and Advanced SAS. Basic Knowledge on Protocol, SAP, Mock shells, Specification.. Excellent communication and interpersonal skills to effectively interact with others
HYDERABAD, INDIA
A minimum of 1 to 3 years of experience in developing nice-looking cutting-edge enterprise web applications with at least a bachelor’s degree in computer science or related field.
Job DescriptionStrong exposure on Core Java, in depth knowledge of using collections, understanding of object-oriented principles and design patterns. Experience in creating web page with JavaScript, jQuery, HTML5 and CSS3. Good understanding of servlets, JSP, page templates, face-lets etc. Excellent in building the application with JSF, JPA, Hibernate. Experience in Primefaces framework is preferred, but okay to have any other jsf framework experience. Good sense of using the themes, colors, UI components. Good UI debugging skills, ability to code and test for all browsers. Understanding of DBMS concepts and be able to write SQL quires. Good foundation in data structures, algorithms, and software design with strong analytical skills. Should be like team player, ready to accept ownership, work independently, research, share and help peers.
ResponsibilitiesExperience with build tools, such as Git, Maven etc. Experience using eclipse, tomee, jboss. Any front-end development frameworks like in Angular, Node js or React etc.