Associate Biostatician - Bengaluru, Karnataka, India - Novasyte

Novasyte

Verified Company

Bengaluru, Karnataka, India

2 weeks ago

Posted by:

Deepika Kaur

beBee Recuiter

Description

BS degree in Statistics or equivalent & 3 years of industry related experience

Or

Master's degree in Statistics or equivalent & 1 year of industry related experience

Must Have

Ability to work successfully within a global crossfunctional teams leading to successful regulatory filings and approvals
Strong verbal and written communications skills.
Ability to be flexible and adapt quickly to the changing needs of the organization.
Ability to organize multiple work assignments and establish priorities.
Good interpersonal skills with peers and adjacent functions (e.g. statistical programming)

BS Specifics (preferred)

Working knowledge of statistical / clinical trials methodology as it relates to clinical development
Relevant prior data analysis planning, execution and delivery experience

The Biostatistician I is a member of cross-functional development teams and contributes (with supervision) to activities that may include development of the statitical methods section of clinical protocols, development of Statistical Analysis and/or Data Presentation Plans, statistical data review, statistical analysis and interpretation.

Also contributes to the development of clinical study/integrated reports, regulatory responses and scientific publications (including abstracts and congresses).

Biostatisticians I's are individual contributors and report to a Global Biometrics & Data Sciences (GBDS) Functional Lead; must be able to work in an environment with supervisory oversight and show willingness to learn and adapt to changing study needs in support of broader team deliveries.

Performs preplanned statistical analyses, e.g. from the SAP or DPP, with supervision
Presents analysis results and interpretations to GBDS team.
Provides internal GBDS review of other SAPs, results, CSRs.
Knowledge of results outside of traditional statistical expertise in the clinical, regulatory and commercial environments and the impact the development team
Engages as a GBDS team member to learn the drug development process
Assists in development of presentations of analyses to key stakeholders
Knowledgeable of statistical methodology and how it might be appropriately applied in trial design and data analysis for clear, concise, highquality results.
Knowledge of statistical / clinical trials methodology as it relates to clinical development
Understanding of data analysis planning, execution and delivery
Understanding of CDISC standards and implementation guides

See above minimum requirements

None

Preferred

Good

Fluent

Yes

Extensive in:

Microsoft Suite

Proficient in:

Yes

Preferred

Strong

Continuously employeed and with companies 1 year or logical explanation

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.

We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.

Learn more at