BioSpace
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Director I, Clinical Development
role at
BioSpace
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, visit abbvie.com.
Job Description The Director I will provide direction and oversight to the design, planning and execution of research activities—including but not limited to clinical trials in Aesthetic Medicine. Participate and lead cross‑functional teams to generate, deliver and interpret high‑quality research and clinical data supporting aesthetic indications and overall asset program strategy. As a clinical development subject matter expert, author, edit and review key sections of research protocols, reports and regulatory submissions.
Responsibilities
Manage the design and implementation of research protocols for clinical development programs in support of the overall Product Development Plan.
Oversee project‑related education of investigators, study site personnel, and AbbVie study staff.
Ensure understanding and compliance with regulatory requirements related to clinical studies, clinician‑reported outcomes, patient‑reported outcomes, and global drug development, specifically in aesthetics.
Contribute to the design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory submissions and responses, and other program documents.
Contribute to the development of a rigorous, cross‑functionally‑aligned, vetted Integrated Evidence Plans in collaboration with matrix team members.
Participate in opinion‑leader interactions related to the disease area(s) and partner with Medical Affairs, Commercial, and other functions as required, consistent with corporate policies.
Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures, and all other quality standards in conducting research.
Position is based in Irvine, CA.
Qualifications
Bachelor’s degree in the sciences; advanced degree (e.g., MS, Ph.D.) preferred.
Ability to provide input and direction to clinical research teams with minimal supervision.
Strong cross‑functional collaboration and leadership skills in a team‑matrixed environment.
Experience managing program budgets and timelines.
Demonstrated ability to select, contract, and manage vendors, ensuring high‑quality and on‑time deliverables.
At least 5 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
Knowledge of clinical trial methodology, regulatory, and compliance requirements in Aesthetic Medicine.
Excellent oral and written English communication skills.
Benefits and Compensation Compensation Range: $200,500 – $382,000 (base pay). Salary will be determined based on geographic location and other factors; may be modified in the future.
Benefits include paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees. This job is eligible to participate in our short‑term and long‑term incentive programs.
Equal Opportunity Employer AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
US & Puerto Rico only – for more information, visit equal‑employment‑opportunity‑employer.
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: reasonable‑accommodations.
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Director I, Clinical Development
role at
BioSpace
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, visit abbvie.com.
Job Description The Director I will provide direction and oversight to the design, planning and execution of research activities—including but not limited to clinical trials in Aesthetic Medicine. Participate and lead cross‑functional teams to generate, deliver and interpret high‑quality research and clinical data supporting aesthetic indications and overall asset program strategy. As a clinical development subject matter expert, author, edit and review key sections of research protocols, reports and regulatory submissions.
Responsibilities
Manage the design and implementation of research protocols for clinical development programs in support of the overall Product Development Plan.
Oversee project‑related education of investigators, study site personnel, and AbbVie study staff.
Ensure understanding and compliance with regulatory requirements related to clinical studies, clinician‑reported outcomes, patient‑reported outcomes, and global drug development, specifically in aesthetics.
Contribute to the design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory submissions and responses, and other program documents.
Contribute to the development of a rigorous, cross‑functionally‑aligned, vetted Integrated Evidence Plans in collaboration with matrix team members.
Participate in opinion‑leader interactions related to the disease area(s) and partner with Medical Affairs, Commercial, and other functions as required, consistent with corporate policies.
Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures, and all other quality standards in conducting research.
Position is based in Irvine, CA.
Qualifications
Bachelor’s degree in the sciences; advanced degree (e.g., MS, Ph.D.) preferred.
Ability to provide input and direction to clinical research teams with minimal supervision.
Strong cross‑functional collaboration and leadership skills in a team‑matrixed environment.
Experience managing program budgets and timelines.
Demonstrated ability to select, contract, and manage vendors, ensuring high‑quality and on‑time deliverables.
At least 5 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
Knowledge of clinical trial methodology, regulatory, and compliance requirements in Aesthetic Medicine.
Excellent oral and written English communication skills.
Benefits and Compensation Compensation Range: $200,500 – $382,000 (base pay). Salary will be determined based on geographic location and other factors; may be modified in the future.
Benefits include paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees. This job is eligible to participate in our short‑term and long‑term incentive programs.
Equal Opportunity Employer AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
US & Puerto Rico only – for more information, visit equal‑employment‑opportunity‑employer.
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: reasonable‑accommodations.
#J-18808-Ljbffr