Sitero - Biostatistician - Clinical Data Management (8-10 yrs)

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have

experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled

solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III

clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all

stakeholders acrossthe clinical research community with an emphasis on ethics, compliance, and innovation.

Job Title : Biostatistician

Location : Bangalore Office Based (Hybrid Model)

Function :

ESSENTIAL DUTIES AND RESPONSIBILITIES :

You would be responsible for :

- Statistical Expertise : Possess a strong understanding of statistical principles and demonstrate strong statistical skills. Provide comprehensive statistical support throughout clinical studies.

- Statistical Analysis and Interpretation : Conduct statistical analyses of clinical data and interpret the results,

focusing on the efficiency and safety of drug molecules or study goals.

- Study Design and Reporting : Experienced in calculating sample sizes, developing concepts and protocols for studies, creating Statistical Analysis Plans (SAP), and preparing clinical study reports, including integrated

summaries for regulatory submissions.

- Regulatory Engagement : Engage with regulatory bodies such as the FDA and EMEA, preparing statistical

documentation and effectively communicating statistical plans and results in professional forums.

- DMC/DSMB Support : Provide support for Data Monitoring Committees/Data Safety Monitoring Boards

(DMC/DSMB), including charter development, SAP, and mock Tables, Listings, and Figures (TLFs) for DSMB

support. This encompasses interim analysis, TLF shells, both blinded and unblinded reports, and organizing

kick-off meetings.

- Regulatory Submission Standards : Solid understanding and implementation of Clinical Data Interchange

Standards Consortium (CDISC) requirements for regulatory submissions, including experience with Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) specifications generation and quality control of datasets.

- SAS Proficiency : Extensive hands-on experience in statistical analysis using SAS, including creating mock shell for tables, listings, and figures (TLFs), and validating TLFs for New Drug Applications (NDA) and Biologics

License Applications (BLA) submissions.

- Client Interaction and Sales Support : Actively engage with clients to understand their statistical and analytical needs, providing expert advice and solutions. Support the sales cycle by contributing to proposals,

presentations, and discussions that showcase our statistical capabilities and how they meet client

requirements.

- SOP Development : Responsible for the creation and updating of Standard Operating Procedures (SOPs)

related to statistical processes and regulatory submissions.

JOB DESCRIPTION :

Company Proprietary & Confidential 2

EDUCATION AND EXPERIENCE REQUIRED :

- MSc or PhD in Biostatistics or Statistics

- 10+ years of experience as Biostatistician and working in a CRO/Pharma/Biotech company

- 3+ years of experience in leading team of biostatisticians and statistical programmers and working in

a CRO/Pharma/Biotech company

- Strong written and verbal communications skills, including proficiency in the English language with

the ability to explain complex statistical concepts to non-statisticians

- Proficient in statistical programming languages such as SAS, R, or Python.

- Proficient in BASE, STAT, MACRO and GRAPH and understanding of database structures, TLFs

proficiency

- Capable of directing and promoting teamwork in a multi-disciplinary team setting

- Strong knowledge of regulatory guidelines and statistical methodology related to clinical

development

- Excellent written and verbal communications

- Coach/mentor new team members to support efficient and quick on-boarding

- Cross functional collaboration & Stakeholder management

- Strong knowledge of ICH guidelines.

PREFERRED SKILLS :

- Good written and verbal communication skills.

COMPENSATION & BENEFITS :

Sitero proudly offers an impressive compensation package and benefits, including a competitive salary,

Variable pay, paid time off, and healthcare and retirement benefits.

EMPLOYMENT TYPE :

- Full Time, Permanent

COMMITMENTS :

- Standard Hours 40 hours per week, one hour lunch, Monday Friday. Additional hours as needed.

- Willing to work in shifts as and when needed.

DISCLAIMER :

Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive

consideration for employment without discrimination on the basis of race, color, religion, sex, sexual

orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law