Associate Director, Aesthetics Clinical Development

AbbVie; Irvine; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in Irvine is seeking an Associate Director to oversee clinical research activities in Aesthetic Medicine. The ideal candidate will drive innovation and provide oversight to clinical trials, ensuring compliance with regulatory requirements. Candidates should hold a Bachelor's degree in sciences, possess strong leadership and collaboration skills, and have at least 7 years of experience in clinical research. The role offers a competitive benefits package and opportunities for professional development.

Benefits

Comprehensive benefits package

Paid time off

401(k) plan

Qualifications

• Minimum of 7 years of overall work experience or equivalent.
• At least 5 years of clinical/research experience in the pharmaceutical/device industry preferred.
• Knowledge of clinical trial methodology and compliance in Aesthetic Medicine.

Responsibilities

• Manage the design and implementation of research protocols.
• Oversee project-related education of investigators and study personnel.
• Ensure adherence to Good Clinical Practices and quality standards.

Skills

Strong leadership skills

Cross-functional collaboration

Knowledge of regulatory requirements

Excellent communication skills

Education

Bachelor's degree in the sciences

Advanced degree (e.g., MS, PhD)

Job description

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 www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more.

With our own research and development team focused on driving innovation in aesthetics, we\'re committed to providing the most comprehensive science-based product offerings available.

The Associate Director 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 section of research protocols, reports and regulatory submissions.

Responsibilities:

• Based on strong medical and scientific experience, knowledge of compliance and regulatory requirements, Allergan Aesthetics customers, markets, business operations and emerging issues, manage the design and implementation of research protocols for clinical development programs in support of the overall Product Development Plan.
• Oversees project-related education of investigators, study site personnel and AbbVie study staff.
• Responsible for understanding and addressing applicable regulatory requirements related to the clinical studies, clinician reported outcomes, patient reported outcomes and global drug development. Specifically in the area of aesthetic development.
• Contributes to 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.
• Participates in opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies.
• Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.

The position is based onsite in Irvine, CA.

Qualifications

• Bachelors degree in the sciences; advanced degree (e.g., MS, PhD) 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.
• Demonstrated ability to select, contract and manage vendor, ensuring high-quality and on time deliverables
• Minimum 7 years of overall work experience or equivalent combination of experience and education.
• Minimum 5 years of clinical/research experience in the pharmaceutical/device industry preferred.
• Knowledge of clinical trial methodology, regulatory and compliance requirements in Aesthetic Medicine.
• Ability to interact externally and internally to support global scientific and business strategy. Must possess excellent oral and written English communication skills.

Additional Information

• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

• This job is eligible to participate in our short-term incentiveprograms.

• This job is eligible to participate in our long-term incentiveprograms

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company\'s sole and absolute discretion unless and until paid and may be modified at the Company\'s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

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https://www.abbvie.com/join-us/reasonable-accommodations.html