Associate Director, Aesthetics Clinical Development

Role overview The Associate Director, Aesthetics Clinical Development at AbbVie Inc. in Irvine provides leadership for clinical research projects in the aesthetics space. This position shapes product development strategies and ensures that regulatory standards are met at every stage. What you will do Direct clinical research initiatives for aesthetic products, guiding studies from concept through execution. Establish strategic priorities for development programs and maintain compliance with regulatory requirements. Refine research methodologies to promote reliable, high-quality outcomes. Collaborate with cross-functional teams to improve patient outcomes and contribute to advancements in aesthetic medicine.

AbbVie is seeking a passionate and innovative Associate Director of Aesthetics Clinical Development to lead our clinical initiatives in the aesthetics sector. This pivotal role involves overseeing clinical trials, collaborating with cross-functional teams, and driving strategic advancements in our aesthetic product pipeline. The ideal candidate will have a strong background in clinical development, exceptional leadership skills, and a commitment to enhancing patient outcomes.

Join AbbVie as an Associate Director of Aesthetics Clinical Development, where you will lead innovative clinical trials and contribute to advancing our aesthetic offerings. In this pivotal role, you will collaborate with cross-functional teams to design and execute clinical strategies that align with AbbVie's commitment to providing high-quality aesthetic solutions.

AbbVie Inc. is seeking an Associate Director, Business Excellence Portfolio Strategy for the Aesthetics division in Irvine. This leadership role centers on shaping portfolio strategy and advancing operational excellence across the business. Role overview The Associate Director will guide strategic initiatives that strengthen product offerings and ensure they align with organizational objectives. Success in this position depends on a strong grasp of market trends and the ability to work collaboratively with cross-functional teams. Key responsibilities Drive portfolio strategy for the Aesthetics division Promote operational excellence to support business goals Enhance product offerings in line with market needs Partner with teams across the organization to achieve results Requirements Strategic leadership experience in a relevant field Understanding of market dynamics within aesthetics or related industries Strong collaboration and communication skills

About the Role The Director of Early Development in Clinical Science will be responsible for developing comprehensive early-stage clinical plans, including program outlines, study designs, and essential clinical documents. This individual will lead cross-functional Study Teams to ensure the successful achievement of study milestones and will represent clinical development during core team and investigator meetings. This position requires close collaboration with various teams such as Clinical Operations, Regulatory Affairs, Medical Affairs, CMC, Finance, and Legal to facilitate efficient and scientifically sound early development clinical initiatives. Key Responsibilities: Own early development clinical deliverables, contributing to protocol development, document authoring, data analysis, and execution decisions to guarantee scientific rigor and operational excellence. Develop clinical plans, including timelines, budgets, and oversight of clinical teams. Draft and critically evaluate key clinical and regulatory documents (protocols, SAPs, CSRs, IBs, clinical value dossiers) to ensure scientific integrity and regulatory compliance. Lead training sessions for study investigators on protocols and clinical trial procedures. Conduct research to create foundational educational materials that guide early development program strategies. Analyze clinical data to support data-driven decision-making. Act as the program lead in early development core teams, investigator meetings, and scientific advisory boards. Engage effectively with internal and external stakeholders, including key opinion leaders (KOLs) and regulatory bodies. Demonstrate and promote essential leadership skills, including innovation, business acumen, results orientation, and a commitment to developing team capabilities. Collaborate with Clinical Operations, Regulatory Affairs, Translational Sciences, Biostatistics, Medical Affairs, and other teams to ensure robust trial design and execution.

Welcome to the opportunity of a lifetime!We appreciate your interest in this role. Please review the details, and if you believe this aligns with your career aspirations, we encourage you to discuss your qualifications with your current manager and HR Business Partner. If you're ready to move forward, apply now, and our Talent Acquisition team will reach out for an interview to get to know you better.- Your Human Resources TeamAbout the RoleThe Director of Early Development in Clinical Science will be instrumental in crafting early development clinical strategies, outlining programs, designing studies, and creating essential clinical documentation. You will take charge of leading cross-functional study teams to achieve study objectives and represent clinical development in key core team and investigator meetings as required.This position demands close collaboration with various teams, including Clinical Operations, Regulatory Affairs, Medical Affairs, CMC, Finance, and Legal, to facilitate effective and scientifically sound early development clinical operations.Key Responsibilities:Take ownership of early development clinical deliverables by actively contributing to protocol development, document creation, data analysis, and decision-making to ensure both scientific integrity and operational excellence.Develop clinical plans that encompass timelines, budgets, and team supervision.Create and critically assess key clinical and regulatory documents, ensuring adherence to scientific rigor and regulatory compliance.Lead and train study investigators on protocol and clinical trial procedures.Research and develop foundational educational materials to support early development program strategies.Analyze clinical data to support evidence-based decision-making.Act as the program lead in early development core teams, investigator meetings, and scientific advisory boards.Engage with internal and external stakeholders, including key opinion leaders (KOLs) and regulatory bodies.Demonstrate and promote essential leadership qualities, including innovative thinking, strong business insight, results-oriented focus, and a commitment to enhancing team capabilities.Collaborate with Clinical Operations, Regulatory Affairs, Translational Sciences, Biostatistics, Medical Affairs, and other departments to ensure robust trial design and scientific rigor.

Purpose:AbbVie is actively seeking a Director for our Aesthetics & Regenerative Medicine HEOR-Strategy team. This pivotal role will spearhead strategic research for both pipeline and on-market products, playing a crucial part in securing approvals, reimbursement, and differentiation in the market. With a diverse portfolio boasting over 30 products in development, including both cash-pay and reimbursed pharmaceuticals and devices, the ideal candidate will possess profound expertise in patient-centered outcomes research, HEOR strategy, and regulatory submissions, encompassing both cash-pay and reimbursed portfolios. This position may involve the management of 1-2 direct reports.Responsibilities:Lead patient-centered outcomes research (PCOR) and collaborate with the clinical development team on co-primary and secondary PRO endpoints necessary for global approvals.Develop and implement PRO strategy, oversee PRO development, and lead global regulatory submissions for drug and device approvals.Craft and execute HEOR strategic plans, which include real-world evidence studies, economic modeling, and creating payer dossiers to facilitate product approvals, market access, and reimbursement strategies.Formulate strategic plans and budgets in collaboration with cross-functional teams, ensuring alignment with overall portfolio objectives.Establish strong partnerships with HEOR Centers of Excellence (COEs) to ensure a cohesive cross-functional HEOR strategy.Oversee the design, execution, and scientific communication of HEOR project findings at conferences and in peer-reviewed journals.Encourage cross-functional collaboration and engage effectively with senior leadership.Demonstrate executive presence while engaging with senior leaders and external Key Opinion Leaders (KOLs).

As the Associate Director of Medical Affairs, you will play a crucial role as a scientific and strategic leader, tasked with shaping and advancing the medical vision for our aesthetics portfolio. This position is fundamental in ensuring the development and execution of medical strategies that enhance patient care, improve clinical outcomes, and align with business goals. You will serve as a central resource for therapeutic expertise, spearhead evidence generation initiatives, and create meaningful medical education, training, and resources. Your leadership will guide strategic medical projects that support new indications, disease states, competitive intelligence, and pipeline products.This role requires onsite presence in Irvine, CA (with in-office days on Tuesday, Wednesday, and Thursday).Lead scientific execution of medical strategies and initiatives for the Aesthetics portfolio.Oversee the creation and implementation of medical education and training programs for both internal and external stakeholders.Identify and analyze insight trends by gathering feedback from various field sources, summarizing findings to provide actionable insights, and communicating trends to the broader therapeutic team.Manage and drive key strategic medical projects aligned with the franchise brand plan, including designing a tactical plan for pipeline products focused on new indications and disease states.Develop and curate scientific resources and materials to enhance external scientific communication, including support for field medical teams and congress presentations, as well as educational initiatives related to medical education, data dissemination, guidelines, and value propositions.Ensure continuous competitive intelligence to guide future strategies and tactics.Support lifecycle management for pipeline products and engage in planning for evidence generation.Contribute actively to medical and brand functional planning, including medical education and external engagement, while providing strategic medical input into core brand and product strategies. Collaborate with the Therapeutic Area Lead to ensure alignment between external communication strategies and both therapeutic area and commercial strategies.

About the Role The Associate Director of R&D Quality Assurance at Tarsus Pharmaceuticals plays a crucial role in overseeing the quality of early-stage contract drug product manufacturers, contract packagers, contract testing labs, contract raw material manufacturers, and contract warehouses. Reporting directly to the Director of Quality Assurance, this position involves reviewing and approving investigations related to production, deviations, and laboratory out-of-specifications (OOS). You will also handle change controls associated with master manufacturing records and testing methods, as well as validation protocols and reports for drug products, APIs, and label specifications. This role additionally supports vendor management, supplier audits, and the formulation of quality agreements. Key Responsibilities: Lead and manage Quality Assurance activities for early-phase clinical development programs (preclinical through Phase I/II). Develop, implement, and maintain Quality Management Systems (QMS) to support early development initiatives. Ensure compliance with global GxP regulations (GCP, GLP, GMP) alongside Tarsus’ internal policies and industry standards. Provide strategic QA insights to cross-functional teams including Clinical Development, Regulatory Affairs, Analytical Development, Supply Chain, and CMC. Act as the QA representative on development project teams and advise on risk mitigation strategies. Contribute to the writing, review, and approval of SOPs, protocols, reports, and regulatory submissions. Process and approve change controls and deviations within Tarsus’ QMS. Review and approve CMO’s master batch records, analytical documents, and validation protocols. Review executed batch records and determine product disposition per internal policies. Participate in CMO and Tarsus operation meetings. Support two/three-arm blinded studies. Engage in vendor calls. Factors for Success: Bachelor’s Degree with 12+ years of experience in the pharmaceutical industry. At least 7 years of experience in Pharmaceutical Quality Assurance. Proficiency in investigations using root cause analysis, CAPA, and CAPA effectiveness. Exceptional attention to detail. Strong technical skills across various platforms. Comprehensive knowledge of Microsoft Office Systems. Analytical skills to interpret statistical data.

Join AbbVie as an Associate General Counsel in the R&D Innovation Legal group, where you will play a pivotal role in guiding our R&D organization through critical legal and regulatory challenges as we strive to deliver groundbreaking products to patients. This position is ideal for an individual who is passionate about creatively addressing emerging issues and providing strategic advice that influences our long-term pipeline strategies. The focus will be on our Specialty and Aesthetics therapeutic areas, ensuring that innovative solutions reach those in need.The R&D Innovation Legal group is part of the broader R&D Innovation and Global Alliances Legal team, situated within the Intellectual Property, Transactions and Innovation Legal Department at AbbVie.Key Responsibilities:Offer strategic legal counsel to senior R&D and corporate strategy leaders regarding regulatory issues that affect pipeline development and product innovation, particularly in light of government pricing programs such as the Inflation Reduction Act.Act as an integral member of disease area strategy teams in Specialty and Aesthetics, focusing on long-term R&D and innovation strategies, with particular attention to pipeline development and FDA considerations.Educate AbbVie’s legal departments and business stakeholders about emerging laws, regulations, and industry trends that impact our portfolio.Identify complex legal challenges within assigned matters, develop innovative solutions, and coordinate with our Intellectual Property, Transactions and Innovation Legal Department for comprehensive strategic advice.Embrace a business-oriented approach to problem-solving, identifying future legal challenges and proposing strategies that optimize results for the company.Provide expert advice to Vice Presidents, Presidents, and Officers, recognized as a trusted advisor in substantive areas of expertise.

AbbVie is seeking a highly skilled Associate Director of Technical Product Development Sciences & Technology to join our innovative team in Irvine, California. In this pivotal role, you will lead and oversee the development of cutting-edge technologies and strategies that drive our product pipeline forward. The ideal candidate will possess a strong background in technical development and a proven track record of managing complex projects in the pharmaceutical industry.

AbbVie Inc. seeks an Asset Strategy Leader to join the Research and Development Aesthetics team in Irvine. This position guides product strategy and drives innovation for the aesthetics portfolio. Role overview The Asset Strategy Leader collaborates with colleagues from various departments to define and sustain the strategic direction for aesthetic products. This work ensures that product plans align with both evolving market needs and AbbVie’s overall goals. Key responsibilities Shape and update product strategies for the aesthetics portfolio Work cross-functionally to coordinate innovation efforts Align product plans with market requirements and company objectives Location This role is based in Irvine.

Dear Candidate,We appreciate your interest in the Vice President of Early Development - Clinical Science position. If you believe this opportunity aligns with your professional aspirations, we encourage you to discuss your qualifications with your current manager and HR Business Partner. Should everything align, please submit your application, and our Talent Acquisition team will reach out to schedule an interview to learn more about you.- Your Human Resources TeamAbout the RoleThe Vice President of Early Development - Clinical Sciences will deliver strategic and scientific leadership for early-stage clinical programs, managing trial direction, design, execution, and data interpretation from first-in-human studies through proof-of-concept and beyond. This role emphasizes the creation of a flexible early development clinical strategy to facilitate innovative trials, requiring creative and forward-thinking approaches to study design, endpoints, and operational strategies. This leader will challenge existing paradigms, employing rigorous scientific judgment and innovative thinking to inform critical development decisions.This position will collaborate cross-functionally with Clinical Operations, Regulatory Affairs, Translational Sciences, Medical Affairs, Finance, and Legal to ensure efficient and scientifically sound early development clinical work. Additionally, this individual will partner closely with the Business Development team and partake in clinical due diligence.Key Responsibilities:Maintain an active, hands-on role in clinical strategy and execution, directly contributing to protocol development, study design decisions, data interpretation, and cross-functional problem-solving to swiftly and accurately assess proof-of-concept in early trials.Provide leadership and strategic oversight in defining study strategies, objectives, scope, and timelines to meet business needs, ensuring alignment among team priorities and initiatives.Keep the leadership team informed of study progress and escalate critical issues within the organization as necessary.Exhibit and promote key leadership competencies, including an innovative mindset, strong business acumen, a results-oriented approach, and a commitment to enhancing the capabilities and capacity of the team.Drive innovation by identifying and integrating cutting-edge technologies and methodologies into early development clinical trial designs.Shape clinical plans, including timelines, budgets, and resource allocations.

Hello! Thank you for your interest in the Associate Director, R&D Quality Assurance position at itcss. We encourage you to review the job details carefully. If this role aligns with your career aspirations, please connect with your current manager and HR Business Partner to discuss your qualifications. If everything checks out, we invite you to apply, and our Talent Acquisition team will reach out for an interview to get to know you better.- Your Human Resources TeamAbout the RoleIn this pivotal role, reporting to the Director of Quality Assurance, you will manage early-stage contract drug product manufacturers, packagers, testing labs, raw material manufacturers, and warehouses from a supplier quality perspective. Your responsibilities will include reviewing and approving investigations related to production, deviations, and laboratory out-of-specifications, as well as overseeing change controls for master manufacturing records, test methods, and validation protocols. You will also support vendor management, audits, and quality agreements.Key Responsibilities:Oversee Quality Assurance activities for early Phase (preclinical through Phase I/II) clinical development programs.Develop and maintain Quality Management Systems (QMS) to support early development activities.Ensure compliance with global GxP regulations (GCP, GLP, GMP) and internal policies.Provide strategic QA input to cross-functional teams including Clinical Development, Regulatory Affairs, Analytical Development, Supply Chain, and CMC.Act as the QA representative on project teams, providing guidance on risk mitigation strategies.Contribute to the writing, review, and approval of SOPs, protocols, reports, and regulatory submissions.Process and approve change controls and deviations within the QMS.Review and approve contract manufacturing organization (CMO) master batch records and validation protocols.Participate in CMO and itcss operational meetings.Support two/three-arm blinded studies and participate in vendor calls.

About the Position The Vice President of Early Development - Clinical Science plays a pivotal role in shaping the strategic and scientific direction of early development clinical programs. This leadership position entails overseeing the design, execution, and data interpretation of clinical trials from first-in-human studies through proof-of-concept. The primary objective is to develop a versatile early clinical development strategy that fosters innovative trial designs, endpoints, and operational tactics. This leader is expected to challenge traditional methods, leveraging robust scientific judgment and creative thinking to guide critical development decisions. This role will require collaboration across multiple functions, including Clinical Operations, Regulatory Affairs, Translational Sciences, Medical Affairs, Finance, and Legal, to ensure the efficient and scientifically sound execution of early development initiatives. Additionally, the VP will partner with the Business Development team and engage in clinical due diligence activities. Key Responsibilities: Actively contribute to clinical strategy and execution, including protocol development, study design, data interpretation, and problem-solving to quickly assess proof-of-concept in early trials. Provide leadership and strategic oversight in study strategy, objectives, scope, and timelines to align the team with common priorities and business needs. Keep the leadership team updated on study progress and escalate critical issues as necessary. Foster a culture of innovation, strong business acumen, and a commitment to team development and capability expansion. Incorporate advanced technologies and methodologies into early clinical trial designs. Develop clinical plans, including timelines and budgets, while overseeing clinical teams. Represent the company in interactions with investigators, regulators, and executive stakeholders. Generate insights that support safe usage, patient targeting, and clinical/commercial positioning. Analyze clinical data from early to mid-stage studies. Contribute as a senior leader within the broader leadership team, influencing strategic decisions. Collaborate with Clinical Operations, Regulatory Affairs, and Translational Sciences to drive clinical advancements.

Greetings! Thank you for considering this opportunity to join our team as the Associate Director of Market Intelligence. We encourage you to carefully review the role details. If this aligns with your professional aspirations, please discuss with your current manager and HR Business Partner to ensure your skills and experiences are a match. Once confirmed, we invite you to apply, and our Talent Acquisition team will reach out to schedule an interview where we can get to know you better.- Your Human Resources TeamAbout the RoleAs the Associate Director of Market Intelligence & Strategy, you will play a crucial role in equipping Tarsus leadership and teams with a comprehensive, integrated perspective of the market and competitive landscape concerning our existing, emerging, and future assets. By synthesizing primary market research, secondary data, and AI-driven analytics, you will provide actionable insights that guide our commercial portfolio and pipeline strategies.Key Responsibilities:Lead enterprise-wide market and landscape intelligence, amalgamating primary research, secondary data, and AI-driven insights to propel strategic decision-making.Continuously monitor third-party catalysts across the industry landscape, including press releases, financial disclosures, earnings calls, corporate presentations, clinical trials, regulatory updates, patents, publications, and media activities.Deliver proactive, scenario-based strategic input for both current products and future pipeline or business development initiatives.Utilize AI and advanced analytics to discern trends, evaluate landscape risks, and foresee market changes.Conduct primary market research (both qualitative and quantitative) to gain deep insights into customer behavior, enhancing XDEMVY performance.Establish and execute the company’s centralized market intelligence processes, governance, and cross-functional communication flows.Collaborate with and align cross-functional teams—such as Commercial, Investor Relations, R&D, HR, Innovation, and Business Development—around shared insights and coordinated responses to market dynamics.Traits for Success:Bachelor’s degree in Life Science, Business, or a related field with 12 years of relevant experience; an MBA or advanced degree is preferred with 10 years of related experience.Proven experience in biotech, pharmaceutical, or healthcare industries is essential.

Join Stanbridge University as the Associate Director of Admissions and lead our dedicated admissions team to drive student recruitment and enrollment efforts. In this pivotal role, you will develop and implement strategies to attract diverse student populations while ensuring a seamless admissions process.As the Associate Director, you will collaborate with academic departments to understand program offerings and communicate these effectively to prospective students. You will oversee the admissions staff, providing mentorship and guidance to enhance their performance and maintain high standards of customer service.

Join AbbVie as the Associate Director of Quality Assurance, where you will play a pivotal role in ensuring the highest quality standards in our products. In this leadership position, you will be responsible for developing and implementing quality assurance strategies while collaborating with cross-functional teams to uphold our commitment to excellence.

The Associate Director of Translational Science at Tarsus Pharmaceuticals, Inc. will lead research efforts aimed at developing new therapies. Based in Irvine, California, this position plays a key role in moving scientific discoveries from the lab toward clinical use. The role involves frequent collaboration with teams across the organization to ensure research aligns with broader company objectives. Key responsibilities Direct translational research projects, guiding them from initial planning through completion Work closely with colleagues in various departments to coordinate research activities with company priorities Share updates on project progress and scientific results with stakeholders in a clear and timely manner Make sure all research supports the organization’s strategic goals

Join AbbVie as an Associate Director of Regulatory Affairs for Chemistry, Manufacturing, and Controls (CMC). In this strategic role, you will lead regulatory submissions and ensure compliance with FDA regulations, facilitating the smooth introduction of innovative therapies.