AbbVie
Associate Director, Statistics - Eye Care
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Associate Director, Statistics - Eye Care
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AbbVie . Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok. Job Description
The Associate Director, Statistics - Eye Care provides statistical leadership for clinical development and life-cycle management strategies for assigned projects, including clinical trials, patient safety, and global medical affairs. The role involves partnering with multidisciplinary experts to advance medicines to patients. This position offers a hybrid work schedule (3 days onsite) at one of the following locations: Irvine, CA Lake County, IL South San Francisco, CA Florham Park, NJ Responsibilities
Support clinical development projects, lead statistical strategies for development and regulatory submissions. Design, analyze, and report on clinical or scientific research programs; develop protocols and analysis plans. Represent the statistical function on project teams, collaborating with Clinical, Regulatory, Patient Safety, and GMA teams to develop strategies. Apply advanced statistical concepts, propose innovative methodologies, and ensure proper analysis execution. Mentor staff, supervise contract statisticians, and support professional development. Develop data presentation strategies, interpret statistical results, and contribute to scientific publications. Serve as the statistical liaison in collaborations with CROs, academic institutions, and regulatory bodies. Ensure compliance with regulatory standards and review regulatory submission documents. Qualifications
MS (10+ years) or PhD (6+ years) in Statistics, Biostatistics, or related field. Strong technical skills, excellent communication, and leadership abilities. Experience in drug development, life-cycle management, and regulatory environments. Experience leading safety-related projects and in experimental and RWE study designs. Additional Information
Includes details on compensation, benefits, and equal opportunity employment policies.
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Join to apply for the
Associate Director, Statistics - Eye Care
role at
AbbVie . Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok. Job Description
The Associate Director, Statistics - Eye Care provides statistical leadership for clinical development and life-cycle management strategies for assigned projects, including clinical trials, patient safety, and global medical affairs. The role involves partnering with multidisciplinary experts to advance medicines to patients. This position offers a hybrid work schedule (3 days onsite) at one of the following locations: Irvine, CA Lake County, IL South San Francisco, CA Florham Park, NJ Responsibilities
Support clinical development projects, lead statistical strategies for development and regulatory submissions. Design, analyze, and report on clinical or scientific research programs; develop protocols and analysis plans. Represent the statistical function on project teams, collaborating with Clinical, Regulatory, Patient Safety, and GMA teams to develop strategies. Apply advanced statistical concepts, propose innovative methodologies, and ensure proper analysis execution. Mentor staff, supervise contract statisticians, and support professional development. Develop data presentation strategies, interpret statistical results, and contribute to scientific publications. Serve as the statistical liaison in collaborations with CROs, academic institutions, and regulatory bodies. Ensure compliance with regulatory standards and review regulatory submission documents. Qualifications
MS (10+ years) or PhD (6+ years) in Statistics, Biostatistics, or related field. Strong technical skills, excellent communication, and leadership abilities. Experience in drug development, life-cycle management, and regulatory environments. Experience leading safety-related projects and in experimental and RWE study designs. Additional Information
Includes details on compensation, benefits, and equal opportunity employment policies.
#J-18808-Ljbffr