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3.0 - 10.0 years
0 Lacs
hyderabad, telangana
On-site
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.,
Posted 3 days ago
8 - 13 years
16 - 31 Lacs
Kolkata, Hyderabad, Bengaluru
Work from Office
Interested candidates may share their resume at heena.gill@iqvia.com Job Description : Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs • Provides programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis • Support the electronic submission preparation and review • Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities • Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers • Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices • Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors • Independently leads and / or performs programming assignments with minimal supervision • Support improvement initiatives
Posted 2 months ago
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