Associate Director Biostatistics in Early Development - Novartis

Promoting Statistical Insights; London; On-site; GBP 70,000 - 110,000; Full time

Job summary

A leading pharmaceutical company is seeking an Associate Director Biostatistics for Early Development in London. This pivotal role involves leading biostatistical activities for clinical trials, ensuring the advancement of innovative therapies. Candidates should possess a PhD or Master's in Biostatistics, and extensive experience in the pharmaceutical industry.

Qualifications

• Extensive experience in biostatistics within the pharmaceutical or biotechnology industry.
• Proven track record of successful contributions to clinical development programs.

Responsibilities

• Lead biostatistical activities for early development clinical trials.
• Collaborate with cross-functional teams to develop statistical strategies.
• Develop and review statistical analysis plans and clinical study reports.

Skills

Statistical methodologies

Communication

Collaboration

Education

PhD or Master's degree in Biostatistics

Tools

SAS

R

Job description

Associate Director Biostatistics in Early Development - Novartis

Are you passionate about making a difference in the world of healthcare? Novartis is seeking a dynamic and experienced professional to join our team in London at The Westworks.

Position: Associate Director Biostatistics, Early Development
Location: London, The Westworks
Job ID: REQ-10028542

About the Role:

As an Associate Director Biostatistics Early Development, you will be a key member of our biostatistics group, you will play a crucial role in the design, analysis, and interpretation of clinical trials for early development programs. Your expertise will contribute to the advancement of innovative therapies and the improvement of patient outcomes.

Key Responsibilities:

• Lead biostatistical activities for early development clinical trials, including study design, data analysis, and interpretation.
• Collaborate with cross-functional teams to develop and implement statistical strategies for clinical development programs.
• Provide statistical expertise and guidance to project teams, ensuring the integrity and quality of clinical trial data.
• Develop and review statistical analysis plans, study protocols, and clinical study reports.
• Stay up-to-date with industry trends and regulatory requirements, ensuring compliance with relevant guidelines.

Qualifications:

• PhD or Master's degree in Biostatistics, Statistics, or a related field.
• Extensive experience in biostatistics within the pharmaceutical or biotechnology industry.
• Proven track record of successful contributions to clinical development programs.
• Strong knowledge of statistical methodologies and software (e.g., SAS, R).
• Excellent communication and collaboration skills.

If you are passionate about biostatistics and early development, and meet the qualifications listed above, then click here to apply now for this exciting opportunity.

Statisticians in the Pharmaceutical Industry Executive Office:
St James House | Vicar Lane | Sheffield | S1 2EX | UK