Medical Director at leverdemo-8 | Irvine, CA

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.

The Director of Medical Affairs Strategy and Education at itcss plays a key role in bridging clinical research and practical healthcare application. Working from Irvine, California, this leader crafts educational strategies that help healthcare professionals understand and use the company’s medical products. The position combines scientific insight, educational planning, and business alignment to ensure medical affairs efforts support larger company goals. Responsibilities Create and deliver medical education programs that translate research findings into everyday medical practice. Lead projects designed to enhance healthcare professionals’ understanding of itcss medical products. Collaborate with teams across the organization to keep educational initiatives in step with corporate strategy. Represent the company at scientific conferences and industry events. Requirements Significant experience in medical affairs, with a focus on strategy and education. Demonstrated leadership skills and experience managing cross-functional teams. Strong written and verbal communication skills.

AbbVie is seeking a dedicated and innovative Scientific Director for our Medical Affairs team in Irvine, California. In this pivotal role, you will lead scientific strategy and execution within the medical affairs function, ensuring the delivery of high-quality scientific information to healthcare professionals. You will work collaboratively with cross-functional teams to advance our therapeutic areas and support the needs of patients.

Greetings! Thank you for considering this exciting opportunity with our team. We encourage you to review the details below. If this role aligns with your career aspirations, please engage with your current manager and HR Business Partner to discuss how your experience and skills are a fit. If all aligns, we invite you to apply, and our Talent Acquisition team will reach out to you for an interview to learn more about you.- Your Human Resources TeamAbout the RoleWe are actively seeking a dynamic and seasoned Regional Director for Field Medical Affairs to spearhead our operations in the Eastern United States. This pivotal role will lead a team of Medical Science Liaisons (MSLs) and serve as a principal architect for scientific engagement, medical operations strategy, and interdepartmental collaboration.The ideal candidate will possess deep expertise in Eyecare, substantial leadership experience within Medical Affairs, and a proven track record of cultivating impactful relationships with Key Opinion Leaders (KOLs) and Eye Care Practitioners (ECPs). This position is crucial for advancing our medical strategy and enhancing collaboration across various teams. The successful candidate will blend scientific knowledge with strong leadership and strategic insight, driving excellence in medical execution while contributing to the overarching objectives of the Medical Affairs organization.Key Responsibilities:Leadership & Team Management:Guide, mentor, and oversee a team of six MSLs, promoting a collaborative, high-performing, and scientifically rigorous environment.Establish clear expectations for the development and execution of territory plans, objectives, and key performance indicators (KPIs) for each MSL.Conduct regular performance reviews, identify skills gaps, and facilitate MSL growth through coaching, training, and career advancement opportunities.Collaborate with the Medical Affairs Operations leadership team to ensure MSL activities are in sync with organizational priorities and strategic initiatives.Strategic Planning & Execution:Act as a disease state and product expert, providing strategic input into MSL educational initiatives and product launch efforts.Contribute to the formulation of Field Medical Strategy and Tactics in alignment with corporate and medical strategic goals.Ensure MSLs are armed with the latest scientific data and clinical information, supporting their integration into both regional and national initiatives.

Join AbbVie as a Scientific Director / Medical Director within our Medical Affairs team specializing in Oncology, focusing on Ovarian Solid Tumor. This pivotal role involves leading innovative strategies in medical science, collaborating with cross-functional teams, and driving impactful research initiatives.

The Director of Medical Affairs Strategy and Education at Tarsus Rx leads the development and execution of medical strategy for the U.S. market. This senior role transforms complex clinical insights into practical approaches for scientific engagement, education, and evidence generation. Based in Irvine, California, the position reports to senior leadership and manages an Associate Director who handles operational and analytical tasks. Collaboration is central to this role. The Director works closely with teams in Medical Affairs, Commercial, Market Access, Regulatory, Legal, Compliance, and Clinical Development to ensure alignment and coordinated action. Medical Strategy and Insight Leadership Own and lead the U.S. Medical Affairs strategy, informed by input from MSLs, scientific engagements, advisory boards, congresses, and cross-functional partners. Conduct regular reviews to synthesize insights, identify knowledge gaps, refine key intelligence topics and questions, and strengthen scientific messaging. Translate findings into recommendations for educational initiatives, evidence needs, and scientific engagement priorities. Prepare and present executive summaries and strategic updates for senior leaders. KOL Engagement and Scientific Advisory Leadership Develop and implement strategies to engage key opinion leaders (KOLs) within Medical Affairs. Set objectives and scientific priorities for Medical Advisory Boards and similar forums. Oversee interpretation of insights and guide cross-functional action planning. Provide strategic oversight and direction for healthcare professional consultant engagements. Congress Medical Strategy and Scientific Leadership Design annual strategies and engagement models for Ophthalmology and Optometry congresses. Lead scientific exchanges, including KOL discussions and one-on-one meetings at major congresses. Manage post-congress synthesis of insights and turn them into actionable strategies.

About the Role We are looking for a highly skilled and strategic Regional Director of Field Medical Affairs to spearhead our initiatives in the East region. This pivotal role involves leading a team of Medical Science Liaisons (MSLs) and acting as a critical agent for scientific engagement, medical operations strategy, and fostering cross-functional collaboration. The ideal candidate will possess extensive expertise in Eyecare, along with a proven track record of leadership within Medical Affairs. They should demonstrate an exceptional ability to establish and nurture relationships with Key Opinion Leaders (KOLs) and Eye Care Practitioners (ECPs). This position is integral to propelling the organization's medical strategy forward and enhancing collaboration across various teams. The chosen candidate will blend scientific knowledge with strong leadership and strategic insight, driving excellence in field medical execution while aligning with the broader objectives of the Medical Affairs organization. Key Responsibilities: Leadership & Team Management: Guide, mentor, and manage a team of six MSLs, cultivating a collaborative, high-performance, and scientifically rigorous environment. Establish clear expectations for the development and implementation of territory plans, objectives, and key performance indicators (KPIs) for each MSL. Conduct regular performance reviews, identify skill gaps, and facilitate MSL development through coaching, training, and career advancement opportunities. Collaborate with the Medical Affairs Operations leadership team to ensure MSL activities align with organizational priorities and strategic goals. Strategic Planning & Execution: Act as a subject matter expert in disease states and products, providing strategic input for MSL educational initiatives and product launch strategies. Contribute to formulating Field Medical Strategy and Tactics consistent with corporate and medical strategic objectives. Ensure MSLs are equipped with the latest scientific data and clinical insights, facilitating their integration into both regional and national initiatives. Collaborate with Medical Affairs Strategy Leads to manage the Medical Strategy Tactical Team (MSTT), ensuring medical affairs insights are transformed into actionable strategies. Work alongside the Field Medical Trainer and Medical Operations Leadership to develop and engage in field medical training, serving as a resource for the field team. Assist with medical conference strategy and planning, representing scientific expertise and collaborating with ECPs at conferences.

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.

Join AbbVie as the Director of Global Regulatory Affairs Strategy, where you will lead strategic regulatory initiatives to drive drug development and approval processes across multiple therapeutic areas. This pivotal role requires a strategic thinker with deep expertise in regulatory frameworks and a passion for innovation in the pharmaceutical industry.

Join Collabera Inc. as an Associate Regulatory Affairs Specialist in Irvine, California. In this role, you will be integral to our regulatory affairs team, supporting the development, implementation, and maintenance of regulatory strategies. Your contributions will be vital in ensuring compliance with federal and state regulations, and you will collaborate with cross-functional teams to facilitate successful product launches.

Join Viant Technology as the Senior Director of Legal Affairs, where you will lead the legal department in a dynamic and innovative environment. As a key member of the executive team, you will provide strategic legal guidance to support our mission of driving growth and ensuring compliance across the organization. You will oversee legal operations, manage risk, and foster a culture of integrity and accountability.

Join AbbVie as an Associate Director of Regulatory Affairs CMC, where you will play a critical role in guiding our regulatory strategies for Chemistry, Manufacturing, and Controls. This position involves leading cross-functional teams to ensure compliance with global regulatory requirements, thereby contributing to the successful development and approval of our innovative therapeutics.

Join AbbVie as an Associate Director of Regulatory Affairs, focusing on Advertising and Promotion. In this pivotal role, you will lead regulatory strategies that align with our commitment to quality and compliance. Collaborate with cross-functional teams to ensure that promotional materials meet regulatory standards and support our innovative product portfolio.

Join AbbVie as the Associate Director of Regulatory Affairs, focused on Advertising & Promotion. In this influential role, you'll lead regulatory strategies for our digital and corporate communications initiatives, ensuring compliance and effectiveness in our messaging.Your expertise will guide the development of promotional materials, providing critical oversight to align with industry standards and regulatory requirements. Collaborate with cross-functional teams to ensure our communications resonate with healthcare professionals and patients alike.

Join Us at BaltAt Balt, we are committed to enhancing the lives of over 150,000 patients by 2026.Our JourneyWith a legacy spanning 45 years, Balt has emerged as a trailblazer in the medical device industry. We work collaboratively with healthcare professionals and institutions around the globe to design innovative medical devices that address critical health challenges. Our products are utilized by physicians worldwide, supported by 13 offices across 11 countries and continually expanding.Since launching one of the first neurovascular intervention devices in 1977, we have developed the most extensive portfolio of medical devices for stroke treatment. Our ambition is to extend our groundbreaking innovations to the peripheral vascular domain.We take pride in our mission and the extraordinary work we accomplish collectively to empower physicians in saving lives.Why Choose Balt? Join a dedicated team focused on making a difference.Your work will have a meaningful impact, embodying our strong sense of pride.Experience a close-knit team culture that is guided by our shared mission, vision, and values.We value recognition, respect, and our diverse community, which are pivotal to our success.Regardless of location, we prioritize your well-being.Are you ready to become a part of our inspiring journey? Don't hesitate—join us!Position Overview – Senior Regulatory Affairs SpecialistRole Summary:The Senior Regulatory Affairs Specialist is pivotal in coordinating and preparing regulatory submissions for both new and modified medical devices, including license renewals and annual registrations. This role requires a seasoned Regulatory professional who can effectively operate independently, identifying and resolving challenges. You will leverage your regulatory expertise to guide cross-functional teams while thinking strategically and creatively to support various projects. You will engage directly with the FDA, Notified Bodies, and Health Canada, as well as interact with international regulatory agencies at the reviewer level on numerous projects and products.Key Responsibilities:Formulate and execute intricate global regulatory strategies.Act as the Regulatory Affairs representative on project teams, collaborating with partners and stakeholders.

About Balt At Balt, our mission is to enhance the lives of 150,000 patients by 2026. Our Story With over 45 years of innovation, Balt stands at the forefront of the medical device industry. We collaborate closely with physicians and healthcare institutions to create state-of-the-art medical devices that are transforming patient care globally. Our extensive product portfolio, which includes some of the first neurovascular intervention devices introduced in 1977, is utilized by healthcare professionals in over 11 countries through our 13 international offices. We are now excited to expand our innovative reach into the peripheral vascular domain. We take immense pride in our mission, our dedicated team, and the impactful work we do together to empower physicians in their life-saving endeavors. Why Join Balt? Become part of a dynamic team committed to making a difference. At Balt, your work holds significant meaning, and pride in our mission is a fundamental part of our identity. We foster a close-knit team environment driven by our strong mission, vision, and values. We prioritize recognition, respect, and a multicultural community as key components of our employee experience, which contribute to our ongoing success. Regardless of location, we care for our employees. Are you ready to contribute to our story? Join us! About this Opportunity – Senior Principal Regulatory Affairs Specialist Description The Senior Principal Regulatory Affairs Specialist is a highly skilled expert responsible for securing and maintaining regulatory approvals and clearances for new and modified medical devices, including license renewals and annual registrations. This role involves serving as a Regulatory representative on multi-disciplinary teams, organizing and leading meetings, and independently identifying and resolving complex issues. You will apply your advanced regulatory knowledge to guide cross-functional teams while demonstrating strategic creativity in support of projects. Direct interaction with regulatory bodies is a key aspect of this role. Job Responsibilities Develop and implement global regulatory strategies for complex, high-risk medical devices, including contingency planning...

About the Role The Medical Science Liaison (MSL) serves as a vital link between Tarsus Pharmaceuticals and the healthcare community. Reporting to our National Director of Field Medical, MSLs are field-based experts who engage in scientific discussions, provide comprehensive education on disease states, and respond to inquiries related to our innovative products. Key Responsibilities: Develop and maintain relationships with key opinion leaders (KOLs) in optometry and ophthalmology within the designated region, ensuring adherence to PhRMA and Tarsus guidelines. Act as the principal point of contact for medical affairs, facilitating peer-to-peer scientific exchanges through both virtual and in-person meetings. Gather and analyze actionable insights from scientific exchanges in the field to inform and enhance medical strategies. Deliver whole practice education to optometric and ophthalmic centers. Provide educational resources for Optometry schools and Ophthalmology residency programs, fostering a deeper understanding of disease states. Guide customers on investigator-initiated trials and medical information protocols upon request. Identify and recommend KOLs for various projects, ensuring compliance with Tarsus policies. Plan and attend scientific sessions at local, regional, and national medical meetings, and schedule KOL engagements. Collaborate with local and regional medical societies in optometry and ophthalmology. Present scientific evidence to the payer community, advocating for the value of our products. Provide leadership on medical affairs projects and initiatives, ensuring alignment with company goals. Continuously optimize training processes, insights gathering, and field medical operations. Host local scientific exchanges and hands-on workshops such as “lid+lash labs.” Engage in collaborative efforts with cross-functional teams, including training and KOL meetings. Support clinical trials as required, collaborating closely with the clinical development team. Oversee territory budget, performance metrics, KOL mapping, and CRM entries. Factors for Success: A Doctorate in Optometry, MD, PharmD, or PhD with expertise in eye care is required. A minimum of 3 years of experience as a Medical Science Liaison in eye care or equivalent clinical experience is preferred.

At Morgan & Morgan, the work we do is significant. For millions across America, we serve as their final line of defense against insurance companies, large corporations, and defective products. Our team of attorneys spans all 50 states, supported by dedicated client support, innovative marketing, and operations teams. Each individual plays a vital role in the fight for consumer rights, united by our singular mission: For the People.SummaryWe invite applications for the role of Medical Malpractice Associate Attorney to join our dynamic MedMal Litigation team. In this position, you will collaborate closely with skilled attorneys, offering crucial support throughout the trial process.

Join AbbVie, a global biopharmaceutical leader, as the Executive Medical Director of Immunology Clinical Development focusing on Respiratory and Pulmonary conditions. In this pivotal role, you will lead innovative clinical development strategies, overseeing the design and execution of clinical trials to drive the advancement of our respiratory therapies. Your expertise will be critical in shaping the future of immunological treatments and enhancing patient outcomes globally.