Are you a skilled biostatistician looking for an exciting career opportunity in the pharmaceutical and clinical research industry? IQVIA, a global leader in healthcare intelligence and clinical research services, is hiring a Biostatistician 2 for its Statistical Services team in Thāne, Mahārāshtra. This is a full-time position with an end date of 17th February 2025. If you have a passion for biostatistics, clinical research, and data analysis, this could be the perfect role for you. Read on to learn more about the job responsibilities, qualifications, and how to apply.
Job Overview
As a Biostatistician 2 at IQVIA, you will play a critical role in the design, analysis, and interpretation of clinical trial data. You will work closely with cross-functional teams to deliver high-quality statistical outputs, ensuring compliance with industry standards and regulatory requirements. This position offers an excellent opportunity to grow your career in biostatistics while contributing to groundbreaking medical research.
Key Responsibilities
The Biostatistician 2 role involves a wide range of responsibilities, including but not limited to:
- Statistical Analysis and Reporting:
- Prepare analysis plans and write detailed specifications for datasets, tables, listings, and figures (TLFs).
- Interpret statistical analyses and contribute to study reports.
- Ensure all outputs meet industry standards and comply with regulatory guidelines such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
- Leadership and Collaboration:
- Act as a statistical team lead on assigned studies, working closely with project teams to deliver results on time and within budget.
- Mentor and train junior staff, providing guidance on statistical methods and best practices.
- Data Management and Quality Control:
- Assist in database design, validation checks, and resolution of data issues.
- Handle database lock and unblinding processes with appropriate supervision.
- Statistical Programming:
- Develop and maintain programming specifications for datasets and TLFs.
- Utilize SAS and other statistical software packages (e.g., StatXact) to perform analyses efficiently.
- Regulatory Compliance and Risk Management:
- Ensure adherence to Clinical Data Interchange Standards Consortium (CDISC) standards.
- Identify and mitigate risks to project delivery and quality.
- Customer Engagement:
- Build and maintain strong relationships with clients, providing statistical support and guidance.
- Participate in bid defenses and contribute to proposal development.
Qualifications and Skills
To be considered for the Biostatistician 2 role, candidates must meet the following requirements:
- Education:
- Bachelor’s degree in Biostatistics, Statistics, or a related field with 1-3 years of relevant experience, OR
- Master’s degree in Biostatistics, Statistics, or a related field with 1-3 years of relevant experience, OR
- Ph.D. in Biostatistics or a related field.
- Experience:
- Intermediate knowledge of statistical principles and methods applicable to clinical trials.
- Proficiency in SAS and familiarity with other statistical software (e.g., StatXact).
- Strong understanding of CDISC standards (e.g., ADaM).
- Skills:
- Excellent written and oral communication skills.
- Strong attention to detail and commitment to quality.
- Ability to manage multiple tasks and projects effectively.
- Problem-solving skills and the ability to work collaboratively in a team environment.
Why Join IQVIA?
IQVIA is a trusted partner to the global life sciences and healthcare industries, offering unparalleled opportunities for professional growth and development. By joining IQVIA, you will:
- Work on cutting-edge clinical research projects that improve patient outcomes worldwide.
- Collaborate with a diverse team of experts in biostatistics, data management, and clinical research.
- Gain exposure to advanced statistical methodologies and regulatory standards.
- Be part of a company that values innovation, quality, and employee development.
