Snr D/ ED Biostatistics

EPM Scientific; Conshohocken (Montgomery County); On-site; USD 260,000 - 320,000; Full time

Job summary

An innovative pharmaceutical company is seeking an Executive Director of Biostatistics to lead biostatistical activities across clinical development phases. This hands-on role involves conducting complex statistical analyses and developing statistical analysis plans while ensuring the quality of deliverables. The ideal candidate will have a PhD in Biostatistics, extensive industry experience, and a proven track record in leadership. This is an exciting opportunity to influence industry standards and drive innovation within a collaborative environment. If you are passionate about biostatistics and looking to make a significant impact, this position is perfect for you.

Qualifications

• 10+ years of industry experience with leadership in biostatistics.
• Strong expertise in statistical methodologies for clinical trials.

Responsibilities

• Lead the biostatistics team and manage statistical deliverables.
• Collaborate with cross-functional teams for clinical development.

Skills

Statistical methodologies

Leadership

Communication skills

Regulatory submissions

Clinical trials

Education

PhD in Biostatistics or related field

Job description

This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$260,000.00/yr - $320,000.00/yr

We have a current opportunity for a Snr D/ ED Biostatistics on a permanent basis. The position will be based in Pennsylvania. For further information about this position please apply.

Report: Chief Data and Analytics Officer

Job Type: Full-Time

Overview

The Executive Director of Biostatistics will be an individual contributor that will lead multiple biostatistical activities, covering all phases of clinical development. This position will be a hands-on role with a combination of conducting complex statistical analyses, developing SAPs and contributing to regulatory documents.

Key Responsibilities:

• Lead and manage the biostatistics team, fostering a collaborative and high-performing environment.
• Provide statistical expertise and strategic input for clinical development plans, study designs, and regulatory submissions.
• Ensure the quality and integrity of statistical deliverables, including protocols, statistical analysis plans (SAPs), and clinical study reports (CSRs).
• Collaborate with cross-functional teams, including clinical development, regulatory affairs, and data management, to support the company's therapeutic portfolio.
• Represent the company in external scientific and regulatory forums, demonstrating leadership and influencing industry standards.
• Drive continuous improvement initiatives within the biostatistics function to enhance efficiency and innovation.

Qualifications:

• PhD in Biostatistics, Statistics, or a related field.
• Minimum of 10+ years of relevant industry experience, with at least 3 years in a leadership role managing a global team.
• Experience in Liver Diseases is preferred, but open to all TAs.
• Strong expertise in statistical methodologies and their application in clinical trials.
• Experience with regulatory submissions and a thorough understanding of worldwide regulatory requirements.
• Excellent communication skills, both written and verbal, with the ability to explain complex statistical concepts to non-statisticians.
• Proven track record of leading high-performing teams and driving innovation in biostatistics.

Seniority level

Director

Employment type

Full-time

Job function

Science

Industries

Pharmaceutical Manufacturing