Senior Biostatistician (India)

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Senior Biostatistician II to join our A-team (hybrid*). The Sr. Biostatistician II (Sr2Bios) supports the statistical analysis and clinical data activities of the Allucent Biostatistics/Statistical Programming team. This position leads projects, writes statistical documents and statistical sections of study documents for simple to moderately complex studies, and provides senior review of statistical documents and outputs. This position may assist in the programming of datasets and outputs using SAS®. The Sr2Bios will regularly interact with other members of the Allucent biostatistics project team and will interact with clients when leading a study.

In this role your key tasks will include:

• Knowledge in clinical research with emphasis in the development and support of the analysis of clinical trial data
• Prepare statistical analysis plans (SAPs) and table, listing, and figure (TLF) mocks for simple to moderately complex studies
• Familiarity with complex statistical methods and concepts
• Provide senior reviews of statistical documents, data, and outputs for simple to moderately complex studies to ensure quality and integrity
• Execute a statistical analysis of any complexity as specified in a protocol or analysis plan
• Interpret and communicate results for complex statistical analyses and outputs
• Develop and/or review the statistical sections of a study protocol for simple to moderately complex studies
• Review statistical sections of a clinical study report to ensure accurate descriptions of statistical methods used and results of analyses
• Provide randomization materials including randomization schedules and treatment kit lists per Allucent SOPs and the sponsor-approved specifications
• Develop or review documents for integrated analyses (e.g. ISS/ISE), including integrated SAPs and statistical sections of integrated study reports
• Support responses to regulatory questions on statistical issues relating to client regulatory submissions
• Working knowledge of SAS® for production and validation of datasets and statistical outputs
• Write and review specifications for complex ADaM or analysis datasets
• Annotate or review annotations of TLF mocks to assist programming efforts.
• Working knowledge of CDISC standards
• Review CRF design to ensure it conforms with the study protocol and analysis needs.
• Knowledge in clinical research with emphasis in the development and support of the analysis of clinical trial dat
• Prepare statistical analysis plans (SAPs) and table, listing, and figure (TLF) mocks for simple to moderately complex studies.
• Familiarity with complex statistical methods and concepts
• Provide senior reviews of statistical documents, data, and outputs for simple to moderately complex studies to ensure quality and integrity
• Execute a statistical analysis of any complexity as specified in a protocol or analysis plan
• Interpret and communicate results for complex statistical analyses and outputs
• Develop and/or review the statistical sections of a study protocol for simple to moderately complex studies
• Review data management documents as requested to ensure the integrity of study data
• Lead simple to moderately complex projects by fulfilling the following responsibilities: communicate with the client and statistical team, set and achieve timelines and milestones, ensure proper execution of the study SAP, monitor programming efforts in collaboration with the lead programmer, and work with management to ensure adequate resourcing
• Lead management of project budgets, the identification of out-of-scope work, and the change order process
• Function as the lead unblinded statistician for studies and manage unblinded tasks including implementation of interim analyses and participation in DMC/safety review meetings
• Accountable for leading biostatistics and programming activities for a program of studies of high complexity and/or of high value.
• Actively support staff learning & development within the company
• Identify, recommend, and execute departmental initiatives, tools, and process solutions to enhance efficiency and quality.
• Review and evaluate biostatistics and statistical programming processes and procedures within the Quality Management System 
• Represent Allucent at proposal bid defences and/or marketing meetings with prospective clients 
• Establish positive relationships with current and future clients.

Requirements

To be successful you will possess:

• Bachelor’s degree; master's degree preferred, in a relevant discipline including, but not limited to, statistics, mathematics, life science, epidemiology, or healthcare .
• Minimum 5 years of relevant work experience.
• Good knowledge of GxP.
• Familiarity with relevant regulations and guidelines.
• GDPR/HIPPA, CFR/CTR/CTD and applicable (local) regulatory requirements. 
• Working knowledge of computer systems, applications and operating systems. 
• Demonstrate critical thinking and analytic skills 
• Strong written and verbal communication skills including good command of the English language.
• Ability to work in a fast-paced challenging environment of a growing company.
• Strong individual initiative.
• Excellent attention to detail and commitment to quality.
• Proficiency with various computer applications such as Word, Excel, and PowerPoint.
• Ability to establish and maintain effective working relationships with co-workers, managers, clients, and vendors.
• Knowledge of SAS.
• Collaborative and client-focused.
• Ability to effectively manage multiple tasks and projects.
• Strong leadership skills.

Benefits

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on location
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via GoodHabitz and internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Disclaimers:

*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”