Associate Director of Admissions

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 …

Join the dynamic team at Stanbridge University as an Admissions Representative. In this pivotal role, you will be the first point of contact for prospective students, guiding them through the application process and providing essential information about our programs. Your enthusiasm for education and commitment to student success will play a crucial role in shaping their academic journeys.

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 AbbVie as an Associate Director of Medical Affairs, where you will play a pivotal role in advancing our mission to improve patient outcomes. In this dynamic position, you will lead innovative medical strategies and collaborate across functions to support our pipeline and portfolio of products.

Join our dynamic team at AbbVie as an Associate Director of Quality Assurance. In this pivotal role, you will oversee quality assurance operations, ensuring that our products meet the highest standards of quality and compliance. You will lead a team in the development and implementation of quality systems and processes, driving continuous improvement initiatives that align with our organizational goals.Your expertise will be crucial in managing audits, regulatory inspections, and ensuring adherence to industry regulations. If you are a proactive leader with a passion for quality and compliance, we encourage you to apply and be a part of our commitment to delivering exceptional healthcare solutions.

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

Tarsus Pharmaceuticals, Inc., is seeking an experienced Associate Director of Clinical Science to lead our clinical development efforts. The ideal candidate will have a strong background in clinical research, particularly in the field of ophthalmology, and a proven track record of successful trial management.In this role, you will be responsible for designing and overseeing clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to drive project success. Strong leadership skills and the ability to communicate effectively with stakeholders at all levels are essential.

Join AbbVie as the Associate Director of Clinical Development in Aesthetics where you will lead innovative projects aimed at enhancing patient care and outcomes. In this pivotal role, you will oversee clinical trials, collaborating with cross-functional teams to ensure compliance with regulatory standards and achieve strategic goals. Your expertise will directly contribute to the advancement of aesthetic therapies and the development of impactful clinical strategies.

Join AbbVie as an Associate Director in our Aesthetics Clinical Development team, where you will play a pivotal role in advancing our innovative aesthetic solutions. In this dynamic position, you will lead the development and execution of clinical strategies, ensuring compliance with regulatory requirements and overseeing clinical trials.As a key member of the team, you will collaborate with cross-functional partners to drive project success, mentor junior staff, and contribute to the overall strategic direction of our clinical programs.

Join our dynamic team at ITCSS as the Associate Director of Clinical Science, where you will play a pivotal role in leading clinical research initiatives. You will oversee the design and execution of clinical studies, ensuring adherence to regulatory standards and the highest quality of scientific rigor.

We are seeking a dynamic and experienced professional to join AbbVie as an Associate Director in the Technical Pharmaceutical Development Sciences & Technology (PDS&T) team. This role will be pivotal in leading innovative projects that enhance our pharmaceutical development capabilities.As the Associate Director, you will oversee a team of dedicated scientists and engineers, ensuring the successful delivery of high-quality pharmaceutical products. Your expertise will drive the development of cutting-edge technologies, streamline processes, and foster a culture of continuous improvement.

The Associate Director of Pharmaceutical Sciences (Drug Delivery) at Tarsus Pharmaceuticals, Inc. plays a key role in shaping the scientific direction of drug delivery and formulation strategies. Reporting to the Senior Director of Pharmaceutical Sciences, this position centers on pre-IND product development, candidate selection, and advancing new drug delivery platforms. The role works closely with teams such as Innovation Lab, Translational Sciences, Pharmaceutical Development, and Analytical Development to move projects from early concept through to candidate selection. Main responsibilities Lead the development of drug delivery strategies across various modalities, including small molecules, biologics, and peptides. Identify opportunities for innovation and collaborate with intellectual property counsel on invention disclosures and patent planning. Assess competitive landscapes and emerging delivery technologies to guide internal innovation efforts. Design, conduct, and interpret laboratory experiments to create and optimize new drug delivery systems, using data to drive platform advancement. Develop formulation and delivery methods to support pre-clinical animal studies. Work with Translational Sciences to analyze in vitro and in vivo data, including PK/PD, bio-distribution, and tolerability, to refine delivery strategies. Represent delivery sciences in program governance and discussions with external partners. Serve as the scientific point of contact for collaborations with external CROs. Manage R&D project budgets and planning. Perform other related duties as assigned. Requirements Ph.D. in Pharmaceutical Sciences, Chemical Engineering, Biomedical Engineering, or a closely related field. Minimum of 8 years of experience in drug delivery and developing new drug delivery platforms from concept through preclinical validation. Experience managing CROs and building external research collaborations. Strong skills in experimental design, data analysis, and technical problem-solving. Track record of platform innovation and contributions to patents in drug delivery. Excellent communication skills, able to present complex technical topics to diverse audiences. Demonstrated leadership and cross-functional project management experience. Location This role is based in Irvine, California, United States.

Role overview itcss is hiring an Associate Director of Pharmaceutical Sciences to focus on drug delivery systems. This position is located in Irvine, California. The role involves leading research and development efforts, overseeing projects from early concept through to product realization, and advancing new pharmaceutical technologies. What you will do Direct R&D initiatives for drug delivery systems and influence product development strategy. Collaborate with teams across different functions to bring scientific concepts into practical applications. Mentor scientists and engineers, fostering creativity and maintaining high standards within the team. Contribute to building and expanding the product pipeline by addressing key healthcare needs through scientific progress. Requirements Extensive experience in pharmaceutical sciences, with a focus on drug delivery. Background in leading R&D teams and managing projects. Strong ability to work across disciplines and explain complex ideas clearly. Proven leadership and mentoring experience with scientists or engineers. This role offers the opportunity to influence the direction of pharmaceutical technology at itcss and contribute to meaningful healthcare solutions.

Join AbbVie as the Associate Director of Aesthetics Clinical Development, where you will lead innovative clinical trials and contribute to the advancement of aesthetic solutions. In this pivotal role, you will collaborate with cross-functional teams to design, implement, and oversee clinical development strategies that align with our commitment to enhancing patient outcomes.

Join AbbVie as an Associate Director of Business Excellence in Aesthetics Portfolio Strategy, where you will play a pivotal role in shaping innovative business strategies and driving excellence within our organization. In this dynamic position, you will leverage your expertise to enhance operational efficiency and contribute to our mission of improving patient outcomes through advanced aesthetic solutions.

Join AbbVie, a global biopharmaceutical company, as an Associate Director of Finance specializing in US Body Contouring. In this pivotal role, you will drive financial strategies that support our innovative product offerings, ensuring our financial objectives are met while navigating the complexities of the healthcare landscape.Your responsibilities will include managing financial planning and analysis, collaborating with cross-functional teams, and providing insightful financial guidance to support decision-making processes. This is an excellent opportunity to influence the direction of a leading company in the aesthetics industry.

About the Role The Associate Director of Market Intelligence and Strategy plays a pivotal role in equipping Tarsus leadership and teams with a cohesive understanding of the market and competitive landscape related to our current, pipeline, and future assets. By integrating primary market research, secondary data, and AI-enhanced analytics, this position provides actionable insights that guide our commercial portfolio and pipeline strategies. Key Responsibilities: Lead comprehensive market and landscape intelligence initiatives, synthesizing primary research, secondary data, and AI-driven insights to support strategic decision-making across the enterprise. Continuously monitor external catalysts in the market, including press releases, financial disclosures (SEC filings, earnings calls), clinical trial updates, regulatory changes, patents, and media activity. Deliver proactive, scenario-based strategic recommendations for both existing products and future pipeline or business development opportunities. Utilize AI and advanced analytics to identify emerging trends, evaluate landscape risks, and predict market shifts. Conduct thorough primary market research (both qualitative and quantitative) to gain deep insights into customer behavior, thereby enhancing XDEMVY performance. Establish and oversee centralized market intelligence processes, governance, and cross-functional communication strategies. Collaborate with cross-functional teams, including Commercial, IR, R&D, HR, Innovation, and Business Development, to align on shared insights and coordinated approaches to market dynamics.

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.

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.

Join AbbVie as a Scientific Director / Medical Director in the Medical Affairs department focused on Oncology. In this pivotal role, you will lead strategic initiatives to enhance our oncology portfolio and provide scientific leadership in clinical development. You will collaborate with cross-functional teams to define and execute medical strategies that align with our commitment to innovative cancer therapies.