Company Description CPVIA is a clinical data analytics solutions company based in Hyderabad (India) specializing in statistical programming outsource and statistical consulting services. Our experienced and expert team focuses on accelerating drug development activities across therapeutic areas with increased quality and optimum cost for pharmaceutical, biotechnology, and medical device companies. Role Description This is a full-time on-site role for a SeniorPrincipal Statistical Programmer at CPVIA in Hyderabad, with flexibility for remote work. The Principal Statistical Programmer will be responsible for statistical programming, data management, creating macros, and providing statistical expertise for various therapeutic areas. Qualifications Minimum 5 years of experience for Senior and 10 years of experience for Principal role in Statistical Programming for clinical trails using SAS Experience on R (especially admiral package) is mandatory as per the client request Data Management and Macro skills Experience in CDISC Data Standardization (SDTMs), ADaM and TLFs Experience in ADaM, TLFs Experience in creating Graphs using SAS or R Experience in (early phase studies, ideally PK/PD, biomarker) or HIV Therapeutic Area is desired. Ability to work independently and collaboratively Strong analytical and problem-solving skills Excellent communication and organizational skills Bachelor's or Master's degree in Statistics, Computer Science, or related field Willing to work in UK/US time zones and the job is based in India How To Apply If you met all the mentioned qualifications above, please send your resumes to info@cpvia.com,
As a Biostatistician at CPVIA, a clinical data analytics solutions company based in Hyderabad, you will play a crucial role in providing statistical programming outsource and statistical consulting services to pharmaceutical, biotechnology, and medical device companies. Your primary responsibility will be to offer internal statistical support by collaborating closely with lab scientists, technicians, and other statisticians/programmers within the team. Your expertise will be instrumental in supporting various drug development activities for our clients. To excel in this role, you must have a minimum of 3-10 years of experience in the pharmaceutical industry. A background in Sciences or Engineering at the university level, complemented with a post-graduate degree in Biostatistics or equivalent statistical experience, is essential. Proficiency in SAS, R (and JMP), and a deep understanding of statistical theory across various methodologies and experimental designs are prerequisites for this position. We are looking for a team player who can effectively communicate and collaborate within multidisciplinary teams. Your role will involve contributing to the development of protocols, SAPs, and TFLs, as well as overseeing studies and ensuring timely delivery. Strong technical skills in power calculation, simulations, and QDM will be beneficial in fulfilling the requirements of this role. If you meet the qualifications mentioned above and are passionate about contributing to the acceleration of drug development activities with top-notch quality and cost-effectiveness, we invite you to share your resume with us at info@cpvia.com. Join our experienced and expert team at CPVIA to make a significant impact on the pharmaceutical and biotechnology sectors.,
As a Biostatistician at CPVIA, a clinical data analytics solutions company in Hyderabad, you will utilize your expertise in statistical programming and consulting to support pharmaceutical, biotechnology, and medical device companies. Your primary focus will be on accelerating drug development activities while maintaining high quality standards and cost efficiency through collaboration with a team of experienced professionals. With a minimum of 3 years of experience in the pharmaceutical industry, you will play a crucial role in providing internal statistical support by closely working with lab scientists, technicians, statisticians, and programmers. Your responsibilities will involve collaborating with various stakeholders to facilitate drug development activities and ensure successful project outcomes. To excel in this role, you are required to hold a university degree in Sciences or Engineering, with a post-graduate qualification in Biostatistics or equivalent statistical experience. You should have a strong grasp of statistical theory, diverse methodologies, and experimental designs. Proficiency in SAS, R (and JMP) is essential, along with effective communication skills to bridge theoretical concepts with practical applications. Being a team player is vital as you will be expected to share knowledge within multidisciplinary teams and contribute to study oversight and delivery. Experience in developing protocols, Statistical Analysis Plans (SAP), Tables, Figures, and Listings (TFL) is advantageous. Additionally, your technical skills in power calculation, simulations, and Quality Data Model (QDM) will be valuable assets in this role. If you meet the qualifications mentioned above and are passionate about making a meaningful impact in drug development, we encourage you to apply by submitting your resume to info@cpvia.com. Join us at CPVIA and be part of a dynamic team dedicated to driving innovation and excellence in clinical data analytics.,