6.0 - 11.0 years

9 - 19 Lacs

Hyderabad

Hybrid

1. Advanced skills in statistical and biostatistical analysis 2. Ability to communicate effectively in the English language in person, by phone and in writing 3. Designs, plans, and execute biostatistical components of clinical studies. 4. Uses statistical methodology to conduct studies and prepares statistical components of protocols. 5. Responsible for the statistical components of reports. 6. Develops statistical analysis plans and reporting specifications for clinical studies. 7. Reviews reports and underpins the results with statistical expertise. 8. Prepares and annotates shell data displays 9. Analyzes and interprets results from clinical studies using sound statistical methodology. 10. Contributes to the development of statistical analysis plans including TFL shells. 11. Performs statistical analyses under the guidance of other statisticians or independently for simple clinical studies. 12. Assists with the review of TFLs, tabulation datasets, and derived datasets. 13. Advanced computer skills and practical knowledge of MS Word, Excel, PowerPoint, and project management software.

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Biostatistician CPVIA

3.0 - 10.0 years

0 Lacs

hyderabad, telangana

On-site

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.,

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The cleaned title from the string Biostatistician is Biostatistician . CPVIA

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.,

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Senior Statistical Programmer IQVIA

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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