What are the responsibilities and job description for the Senior Biostatistician position at TekOne IT Services Pvt. Ltd.?
Key Responsibilities
- Statistical Analysis:
- Plan, supervise, implement, and monitor statistical processes for multiple clinical trials.
- Apply advanced biostatistical methods and techniques to clinical trial data.
- Clinical Trial Design:
- Collaborate on clinical trial design and scenario planning, ensuring statistical methodologies are aligned with regulatory requirements.
- Bayesian Statistics:
- Utilize expertise in Bayesian statistics to enhance trial design and analysis.
- Statistical Software Proficiency:
- Employ statistical software (SAS and/or R) for data analysis and reporting.
- Collaboration:
- Work closely with program partners and stakeholders to deliver statistical outputs for one or more clinical trials.
- Clearly communicate complex statistical concepts and findings in both written and verbal forms.
- Team Dynamics:
- Act as a team player with a focused attitude, contributing to a collaborative work environment.
- Work autonomously while integrating into a cross-disciplinary team in a fast-paced biotech setting.
- Educational Background:
- Master’s degree or Ph.D. in Statistics or a related field.
- Experience:
- Minimum of 6 years of experience in biostatistics, which may include doctoral research.
- Demonstrated expertise in drug development and clinical trials within a regulatory environment.
- Extensive experience in the Pharma or Biotech industry.
- Technical Skills:
- Strong command of biostatistics and its application to clinical trials.
- Proficiency in statistical software, particularly SAS and/or R.
- Soft Skills:
- Excellent communication skills, with the ability to explain complex statistical concepts clearly.
- Strong problem-solving abilities and a proactive approach to challenges.
- Ability to work effectively both independently and as part of a team.
