Vice President, Biometry

Vacancy Details

The Vice President of Biometry at Parabilis Medicines will oversee the biometrics organization, ensuring the integrity and quality of clinical trial data and analyses. This role is critical for supporting clinical development programs from early-phase through regulatory submission.

About the role

Lead and develop the Biometrics organization, including biostatistics, programming, data management, clinical data science, and Real-World Data. Ensure high-quality deliverables across all clinical programs and foster a culture of scientific rigor, accountability, collaboration, and innovation.

Responsibilities

• Lead and develop the Biometrics organization, including biostatistics, programming, data management, clinical data science, and Real-World Data.
• Foster a culture of scientific rigor, accountability, collaboration, and innovation.
• Oversee design and implementation of statistical methodologies for clinical trials.
• Champion innovative methodologies, including adaptive and model-based approaches, to support efficient and agile drug development.
• Provide strategic input into drug development strategies in collaboration with program-level and functional leadership, working closely with Clinical Development, Clinical Operations, and Translational Medicine.
• Ensure the integrity, high quality, and traceability of clinical trial data and the accuracy of all statistical analyses, leading to compliant deliverables in biometry.
• Lead and support biometrics interactions with global health authorities.
• Establish and maintain vendor partnerships ensuring quality and timely delivery of outsourced biometrics activities.

Requirements

• Doctoral degree in Biostatistics or related field.
• 15+ years of biometrics experience within the biotech or pharmaceutical field.
• Proven track record of leading, building, and managing teams.
• Demonstrated record of fostering creativity, productivity, and execution with urgency, teamwork, and accountability.
• Deep knowledge of clinical trial design, regulatory requirements, and statistical environment.
• Excellent problem-solving skills, strategic thinking, and ability to work in a fast-paced, collaborative environment.
• Outstanding interpersonal skills, self-awareness, and ability to manage team dynamics.
• Ideal experience in more than one therapeutic area and direct experience with innovative Phase 1-3 clinical study designs for oncology.
• Comfort with model-based drug development and agile drug development.
• Appreciation for observational methodologies.
• Ability to articulate complex methodologies to senior executives for their understanding.
• Demonstrated use of AI tools in your current role and responsibilities.
• Advanced or innovative use of AI.

Qualifications

• Doctoral degree in Biostatistics or related field.
• 15+ years of biometrics experience within the biotech or pharmaceutical field.
• Proven track record of leading, building, and managing teams.
• Demonstrated record of fostering creativity, productivity, and execution with urgency, teamwork, and accountability.
• Deep knowledge of clinical trial design, regulatory requirements, and statistical environment.
• Excellent problem-solving skills, strategic thinking, and ability to work in a fast-paced, collaborative environment.
• Outstanding interpersonal skills, self-awareness, and ability to manage team dynamics.
• Ideal experience in more than one therapeutic area and direct experience with innovative Phase 1-3 clinical study designs for oncology.
• Comfort with model-based drug development and agile drug development.
• Appreciation for observational methodologies.
• Ability to articulate complex methodologies to senior executives for their understanding.
• Demonstrated use of AI tools in your current role and responsibilities.
• Advanced or innovative use of AI.

Skills

• Doctoral degree in Biostatistics or related field.
• 15+ years of biometrics experience within the biotech or pharmaceutical field.
• Proven track record of leading, building, and managing teams.
• Demonstrated record of fostering creativity, productivity, and execution with urgency, teamwork, and accountability.
• Deep knowledge of clinical trial design, regulatory requirements, and statistical environment.
• Excellent problem-solving skills, strategic thinking, and ability to work in a fast-paced, collaborative environment.
• Outstanding interpersonal skills, self-awareness, and ability to manage team dynamics.
• Ideal experience in more than one therapeutic area and direct experience with innovative Phase 1-3 clinical study designs for oncology.
• Comfort with model-based drug development and agile drug development.
• Appreciation for observational methodologies.
• Ability to articulate complex methodologies to senior executives for their understanding.
• Demonstrated use of AI tools in your current role and responsibilities.
• Advanced or innovative use of AI.

Benefits

Parabilis offers a comprehensive suite of competitive benefits designed to support employees' overall well-being, including an annual target bonus, equity, and a robust health and wellness program. The company is committed to promoting an inspiring and flourishing working environment for all employees.

Pay

The base salary target for this position is $340,000-$380,000 per year, depending on experience, qualifications, and internal practices.

Schedule

Not specified.