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Associate Biostatistician - Graduate Hiring

Pharmaceutical Product Development (PPD)

IN-Bengaluru-Bengaluru IN Valence Block

Provides statistical support in terms of analysis database creation, statistical analyses, and creation of formatted statistical analysis tables and summaries. Supports a lead team member to learn lead responsibilities.Becomes familiar with the activities outlined in the department's Standard Operating Procedures and Working Practice Documents and contributes changes as needed. Learns and follows departmental procedures for statistical analyses and programming work.• Supports a lead statistician to learn lead responsibilities.• Creates analysis databases. Coordinates with programmers and data management personnel as to database maintenance, updating and documentation.• With mentoring, provides sample size calculations and review protocols for completeness, appropriateness of clinical design, and sound statistical analysis. • With mentoring, provides randomization schemes and appropriate documentation.• With mentoring, develops statistical analysis plan including table and listing specifications.• Programs/validates statistical tables. Provides proper documentation and oversees the work of others who also assist in programming/validating.• Participates in sponsor meetings and interacts with other departmentsProvides statistical support in terms of analysis database creation, statistical analyses, and creation of formatted statistical analysis tables and summaries. Supports a lead team member to learn lead responsibilities.Becomes familiar with the activities outlined in the department's Standard Operating Procedures and Working Practice Documents and contributes changes as needed. Learns and follows departmental procedures for statistical analyses and programming work.• Supports a lead statistician to learn lead responsibilities.• Creates analysis databases. Coordinates with programmers and data management personnel as to database maintenance, updating and documentation.• With mentoring, provides sample size calculations and review protocols for completeness, appropriateness of clinical design, and sound statistical analysis. • With mentoring, provides randomization schemes and appropriate documentation.• With mentoring, develops statistical analysis plan including table and listing specifications.• Programs/validates statistical tables. Provides proper documentation and oversees the work of others who also assist in programming/validating.• Participates in sponsor meetings and interacts with other departmentsPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’). Master's degree in statistics, biostatistics, mathematics or related field In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:• Basic SAS® programming skills including a thorough understanding of macros, SAS/GRAPH, SAS/STAT, and data step programming• Capable of promoting teamwork in a multi-disciplinary team setting• Fundamental understanding of basic statistical procedures• Basic knowledge of clinical trials database structure• Essential written and verbal communications skills• Good organizational skills with the ability to adapt and adjust to changing priorities• Positive attitude and the ability to work well with othersPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’). Master's degree in statistics, biostatistics, mathematics or related field In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:• Basic SAS® programming skills including a thorough understanding of macros, SAS/GRAPH, SAS/STAT, and data step programming• Capable of promoting teamwork in a multi-disciplinary team setting• Fundamental understanding of basic statistical procedures• Basic knowledge of clinical trials database structure• Essential written and verbal communications skills• Good organizational skills with the ability to adapt and adjust to changing priorities• Positive attitude and the ability to work well with others

Job posted: 2020-10-05

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