Associate Director of Medical Affairs

Dane Street, a leader in medical consulting services, is seeking a dedicated Associate Medical Director to support the needs of one of our prominent clients. This role requires engaging directly with client Medical Directors, assisting in the auditing of cases as necessary, and reviewing complex case disputes. The ideal candidate will possess multiple state …

Join WelbeHealth as an Associate Medical Director where you will play a pivotal role in enhancing the quality of care for our patients. You will collaborate with a dedicated team to develop and implement innovative healthcare solutions that prioritize patient well-being and satisfaction.

Opportunity Overview: Cohere Health is on the lookout for skilled physicians with a deep understanding of Cardiology and Vascular medical topics to spearhead our innovative Cardiology program. In this role, you will assess the medical appropriateness of services by reviewing clinical information and applying evidence-based guidelines. As a key member of our team reporting directly to the Medical Director of Cardiology, you will play a pivotal role in a rapidly growing organization dedicated to enhancing the health of millions of patients. We thrive in a dynamic environment that rewards quick learners, hands-on contributors, and effective communicators from diverse backgrounds. Your Responsibilities: Collaborate with the clinical development team to evaluate and refine the company’s clinical decision guidelines and evidence-based literature. Provide expert insights on content and initiatives aimed at influencing physicians in cardiovascular care to enhance the quality of patient outcomes. Conduct timely medical reviews in line with Cohere’s high standards for quality and timeliness. Utilize your clinical expertise to make evidence-based clinical determinations. Document all communications and decision-making processes clearly and accurately in Cohere workflow tools, ensuring clarity for both members and providers. Follow established templates for decision documentation during case reviews. Engage in peer-to-peer discussions with treating providers to clarify clinical information and explain review outcomes, including feedback on alternative treatments based on medical necessity criteria and evidence-based research. Exhibit the highest standards of professionalism, accountability, and service in your interactions with Cohere colleagues and providers. Assist in projects aimed at building the team’s clinical expertise and efficiency, as assigned. Contribute to operational improvements and enhance member/provider experiences related to clinical review tasks, as needed. Qualifications: U.S.-based residency in Internal Medicine complemented by a fellowship in Cardiology. Board certification (MD or DO) with an active, unrestricted state medical license; all required credentials must be maintained. A minimum of 5 years of clinical practice beyond residency/fellowship in Internal Medicine or Cardiology. At least 1 year of managed care utilization review experience is preferred. Membership in national and/or regional specialty societies is a plus. Licensure in FL, MN, and other states is beneficial.

Innovators Wanted Are you ready to achieve the extraordinary? If this excites you, keep reading. In 2015, we introduced an innovative "moneyball for biotech" strategy, integrating promising early-stage research from academia under a unified financial umbrella to mitigate risk and catalyze innovation. This approach empowers small teams of experts to steer scientific breakthroughs. We are committed to bridging gaps in rare disease treatment and developing transformative medicines for patients with unmet medical needs as swiftly as possible.Together, we redefine possibilities, challenge the status quo, and inspire individuals to tackle complex challenges. If you are someone who challenges norms, we invite you to join our team and collaborate with some of the most esteemed professionals in the industry. At BridgeBio, we embrace curiosity and experimentation, including the ethical and thoughtful application of AI to enhance clarity, efficiency, and quality of work. Key ResponsibilitiesThe Associate Medical Director, Endocrinology will play a pivotal medical and scientific leadership role within the U.S. Medical Affairs team. This position will support the development and execution of the Medical Affairs strategy for encaleret across clinical development initiatives, including autosomal dominant hypocalcemia type 1 (ADH1) and chronic hypoparathyroidism, with an emphasis on launch readiness and lifecycle planning, informed by scientific rigor and patient-centered decision making.This role will collaborate closely with Clinical Development, Scientific Communications, Congress Operations, Regulatory, Commercial, Patient Advocacy, and Field Medical teams to facilitate trial execution, data disclosure, publication planning, peer-to-peer scientific exchanges, and coordinated congress strategies and materials.

Join WelbeHealth as an Associate Medical Director, where you will champion innovative healthcare solutions and lead a dedicated team in delivering high-quality patient care. In this pivotal role, you will collaborate with various stakeholders to enhance our clinical programs and ensure the best outcomes for our patients.

At Real Chemistry, our mission to enhance global health is not merely an ambition; it's our daily commitment. Our focus on healthcare transformation is rooted in a unique combination of profound scientific knowledge, human-centered innovation, and AI-powered insights, creating an environment where creativity flourishes and our team is dedicated to making an impact. As a worldwide agency, we deliver comprehensive healthcare communication and marketing services to leading clients in the pharmaceutical and biotech sectors.Our culture at Real Chemistry, known as #LifeatRealChem, is deeply anchored in our people. We believe in the power of collaboration, striving for excellence not just for our clients but for every team member. Whether you're an experienced expert or embarking on your career, if you share our enthusiasm for healthcare and connection, we encourage you to explore our opportunities.Discover your purpose. Embrace innovation. Experience #LifeatRealChem.Real Chemistry is on the lookout for a skilled and energetic Associate Medical Director to collaborate with our Medical Affairs and Promotional teams. This position offers the chance to spearhead the creation of innovative, impactful medical content that enhances healthcare provider education and improves patient outcomes.In this role, you will utilize your expertise in medical writing and scientific storytelling to produce influential materials across various therapeutic areas. You will engage with cross-functional teams and nurture solid client relationships to uphold excellence in all facets of our projects.

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.

We are seeking a dynamic and experienced Associate Medical Director specializing in Clinical Research within the Cardiovascular field. In this role, you will collaborate with a diverse team of professionals to lead and oversee clinical trials, contribute to the development of innovative therapies, and ensure compliance with regulatory standards. Your expertise will be crucial in advancing our research initiatives and enhancing patient outcomes.

Job Title: Associate Medical Director - Gynecologic Cancer Location: Remote with approximately 30% domestic and international travel Position Summary: Join Natera as an Associate Medical Director in Oncology and play a pivotal role in revolutionizing cancer care. In this high-impact leadership position, you will lend your medical expertise to Natera's oncology portfolio, working collaboratively with cross-functional teams in research, development, commercial, and medical affairs. Your focus will be on maintaining the scientific integrity and facilitating the clinical adoption of our innovative oncology testing solutions. Primary Responsibilities: Clinical Development: Partner with the Sr. Medical Director, Oncology to drive the clinical development of ctDNA-based diagnostics. Lead the formulation and execution of clinical strategies for Natera's oncology products. Medical Education and Communication: Manage medical education initiatives and scientific communications directed at healthcare providers regarding Natera's oncology solutions. Collaborate with the commercial team to craft and present impactful medical messages for our oncology products. Representation and Advocacy: Represent Natera at various medical conferences and industry events, whether in-person or virtual. Encourage a culture of scientific excellence and intellectual curiosity within the oncology team. Research and Development: Work closely with research and development teams on clinical trial design, data analysis, and publication efforts. Key Skill Sets / Responsibilities: Gynecologic Cancer-Specific Expertise: Comprehensive understanding of Gynecologic Cancer, with the capacity to devise and implement strategies tailored to this field. Provide expert guidance and support on Gynecologic oncology cases and clinical trials. Broad Oncology Knowledge: Ability to discuss various histologies and indications, ensuring extensive knowledge across the oncology spectrum. Stay abreast of the latest advancements in different cancer types and incorporate this knowledge into Natera’s oncology products. Cross-Disciplinary Collaboration: Engage with diverse teams across the organization to foster innovation and drive progress in oncology initiatives.

ABOUT THE ROLE:The Associate Director of Medical Information is a vital role within our Medical Information Contact Center (MICC) team. This position is crucial in ensuring that healthcare professionals, patients, caregivers, and payers receive prompt, scientifically accurate, and evidence-based information regarding pharmaceutical products. Additionally, the role involves managing adverse events and product complaints, contributing to client success through effective oversight and management of client relationships.KEY RESPONSIBILITIES:People Management: Lead and develop a team of Medical Information Specialists and Managers, providing mentoring, coaching, and support for their professional growth. Oversee recruitment efforts to build a high-performing team.Client Management & Operations: Ensure client satisfaction through strategic oversight, implementation of operational strategies, and regular communication. Monitor workload and staffing to optimize team performance and maintain service levels.Training & Development: Design and execute comprehensive training programs for MICC staff to enhance their skills and ensure high-quality service delivery.

Innovators Wanted Have you ever accomplished what seemed impossible? If this thought excites you, keep reading...In 2015, we revolutionized the biotech landscape with a

Role Overview The Associate Director, Global Medical Operations at Italfarmaco provides operational leadership within Global Medical Affairs. This remote role works closely with both global and regional medical teams to plan and deliver key medical activities. The position emphasizes hands-on execution and efficient coordination, supporting a range of projects from advisory boards to digital initiatives. Success in this role requires adaptability, strong collaboration skills, and the ability to build effective cross-functional relationships in a biotech setting. Key Responsibilities Lead planning and execution of Global Advisory Boards. Coordinate with local vendors and Legal/Compliance to meet business needs, manage logistics, ensure regulatory compliance, handle contracting, maintain FMV alignment, and document insights. Manage logistics for 3–4 global congresses each year, working with Global Scientific Communications on booth operations, symposium support, onsite coordination, and operational deliverables. Collaborate with IT to oversee the global insights process and digital framework. Facilitate structured insights capture, analysis, dashboard reporting, and sharing across regions to inform global strategy. Support governance for Global Grants & Giving, including workflow review, due diligence documentation, and compliance alignment. Assist with External Expert Engagement in partnership with Legal/Compliance, ensuring FMV standards, proper contracting, and tracking of local regulatory requirements. Partner with IT to advance digital medical initiatives, such as SharePoint governance, dashboard development, process optimization, and workflow automation. Manage logistics and operations for biannual All Medical Summit Meetings, ensuring thorough planning, cross-functional coordination, and smooth execution.

Innovators Wanted Have you ever done the seemingly impossible? If that challenges your imagination, keep reading. In 2015, we revolutionized the biotech landscape with a groundbreaking financial model that pools promising early-stage research from academia. This model not only mitigates risk but also ignites innovation. Our mission is to advance life-saving medicines for patients with rare diseases swiftly and effectively. We are pioneers at BridgeBio, encouraging our team to redefine boundaries and empower problem-solving through curiosity and experimentation, including the ethical integration of AI to enhance our work. What You Will DoThe Associate Director/Senior Medical Science Liaison (MSL) plays a pivotal role in nurturing scientific relationships with external experts, providing clinical insights, and acting as a strategic collaborator with both internal teams and the broader medical community. We seek an individual who excels in dynamic settings, known for their determination, creativity, and unwavering commitment to excellence.With a solid scientific foundation and a dedication to supporting individuals with rare diseases, the Senior MSL will establish trusted partnerships with key opinion leaders (KOLs), facilitate scientific dialogue, and work cross-functionally to propel internal initiatives forward. This position is essential in advancing Medical Affairs strategies by delivering healthcare professional insights and fostering collaboration.

Innovators Needed Have you ever pushed the limits of what’s possible? If the thought excites you, we encourage you to keep reading. Since 2015, we have adopted a revolutionary “moneyball for biotech” strategy, merging diverse early-stage research endeavors into one financial framework to minimize risks and foster innovation. This model empowers small teams of experts to spearhead scientific advancements. We are committed to bridging the gap in rare disease treatment by rapidly developing transformative medicines for patients facing unmet medical needs. Join us as we challenge conventional thinking, redefine possibilities, and empower individuals to tackle challenges head-on. If you’re a trailblazer, collaborate with some of the brightest minds in the industry. At BridgeBio, we celebrate curiosity and innovation, including the ethical integration of AI to enhance our work’s clarity, speed, and quality. Role OverviewThe Associate Director/Senior Medical Science Liaison (MSL) is pivotal in fostering robust scientific relationships with external experts, delivering critical clinical insights, and acting as a strategic ally to both internal teams and the medical community. We seek a candidate who thrives in fast-paced environments, demonstrating resilience, resourcefulness, and an unwavering commitment to excellence.With a solid scientific background and a dedication to supporting individuals with rare diseases, the Sr. MSL will cultivate trusted partnerships with key opinion leaders (KOLs), facilitate scientific discussions, and collaborate across functions to propel internal initiatives forward. This role is essential in advancing the Medical Affairs strategy and operational initiatives.

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a leading biopharmaceutical organization dedicated to the formulation, development, and commercialization of cutting-edge therapies targeting diseases and conditions of the eye through its innovative bioresorbable hydrogel-based technology, ELUTYX™. With a robust pipeline of drug delivery solutions, we are positioned to transform the standard of care and establish ourselves as a frontrunner in the ophthalmic industry.At our headquarters in Bedford, MA, we cultivate a vibrant corporate culture that empowers our employees to thrive and accomplish their professional aspirations. We promote innovative thinking, cross-departmental collaboration, and creativity.Position Overview:The Associate Medical Director plays a pivotal role in medical affairs, supporting the development and lifecycle of groundbreaking retinal therapeutics. Acting as a primary medical and scientific liaison for internal teams and external partners—including retina specialists, investigators, and key opinion leaders (KOLs)—this role contributes significantly to evidence generation, scientific dialogue, and medical decision-making throughout the drug development continuum. The ideal candidate will be an expert in retinal clinical research, responsible for co-developing and executing scientific strategies for medical collaborations, spanning clinical development (phases 1-3), post-marketing studies, and payer-informed research initiatives. The Associate Medical Director will also enhance clinical trial enrollment through strategic engagement in committees and advisory boards, working closely with Clinical Operations.Key Responsibilities:Serve as a scientific authority and external medical representative in the retina space, engaging proactively with retina specialists, investigators, and KOLs.Foster and sustain long-term scientific relationships with prominent thought leaders in retinal disease.Lead complex scientific discussions regarding mechanisms of action, clinical data, trial design, and unmet medical needs.Function as a medical partner to Clinical Development, Regulatory, Commercial, and Market Access teams.Translate external insights into actionable internal recommendations to shape development and lifecycle strategies.Support internal training initiatives and contribute to the education of cross-functional teams.

About This Role: As the Associate Director of Field Medical Operations & Enablement, you will play a pivotal role within the Scientific Medical Affairs (SMA) team at Freenome. Your leadership will establish the operational framework that empowers our medical affairs team to operate at maximum efficiency. This position combines high-level strategic program management with hands-on execution, including orchestrating global conferences, managing advisory boards, and innovating the application of AI-driven tools for disseminating medical insights and developing content for Key Opinion Leader (KOL) engagement. You will be the key architect behind our field medical strategy, ensuring that our teams are well-equipped, our processes adhere to compliance standards, and our insights are effectively integrated across Freenome's operations. This position reports directly to the VP of Field Medical, Advocacy, and Medical Affairs Operations and offers a flexible Hybrid or Remote work environment.

Innovators Needed Are you ready to take on challenges that seem impossible? If this thought excites you, keep reading! In 2015, we introduced a revolutionary approach to biotech by consolidating promising early-stage research from academia under a unified financial umbrella. This innovative model empowers small teams of experts to lead groundbreaking advancements in rare diseases, developing transformative medicines for patients with urgent needs as swiftly as possible. At BridgeBio, we embrace curiosity and experimentation, including the ethical and thoughtful application of AI to enhance clarity, speed, and quality of our work. Join us in redefining the future of biopharma as we challenge the status quo and unlock new possibilities.Role OverviewThe Associate Director/Senior Medical Science Liaison (MSL) will play a pivotal role in forging robust scientific relationships with external experts, delivering clinical insights, and collaborating strategically with both internal teams and the wider medical community. We seek a dynamic individual known for their perseverance, resourcefulness, and commitment to excellence.With a solid scientific foundation and a dedication to supporting those affected by rare diseases, the Senior MSL will cultivate trusted partnerships with key opinion leaders (KOLs), facilitate scientific discussions, and work cross-functionally to promote internal initiatives. This crucial role directly supports the Medical Affairs strategy by enhancing scientific exchange and collaboration.

Join our dedicated team at PetVet Care Centers, where our mission is to enhance the lives of both animals and their human companions through outstanding and empathetic veterinary care at every stage of their journey.Because life is better with pets.We are committed to delivering the Ultimate Care Experience — for every pet, every client, every time. This commitment begins with our Culture of Care, prioritizing the support of our team members just as much as that of the pets and clients we serve.With over 420 locally led hospitals and a workforce of more than 11,000 team members nationwide, we provide:Local autonomy complemented by national supportCareer advancement and development opportunitiesA collaborative and inclusive environment that prioritizes your wellbeingWe care for you, just as you care for pets.Position OverviewThe Animal Hospital of Redondo Beach is actively seeking a skilled Medical Director Veterinarian to join our esteemed team. For over 25 years, we have provided families and their cherished pets throughout Los Angeles County — including Redondo Beach, Torrance, Hermosa Beach, and the South Bay area — with exceptional veterinary care. Our impressive 4.8-star Google review underscores our dedication to client and patient satisfaction. This is a unique chance to expand and personalize your practice.If you are aspiring for a leadership position, our Medical Director role is an ideal fit. Candidates are eligible for an annual Medical Director Stipend of $10,000 along with a higher production percentage.We encourage Associate Veterinarians to apply and become part of our team! Opportunities for Full-Time, Part-Time, and Relief positions are available! (Salary commensurate with experience)Our Medical Director compensation package includes:Starting base salary ranging from $225,000 to $250,000Attractive sign-on bonus up to $100,000Generous Quarterly Production Plan with no deficit carryoverMonthly Medical Director StipendRelocation bonuses available3 weeks of Paid Time Off

POSITION SUMMARY:As the Associate Director of Medical Strategy, you will leverage your profound understanding of the life sciences industry to transform complex scientific and clinical data into actionable insights. Your critical thinking and strategic mindset will drive the development of recommendations that enhance the client’s brand positioning and address intricate business challenges. You will excel in managing multiple projects simultaneously while ensuring high-quality deliverables.KEY RESPONSIBILITIES:Provide strategic insights for the development of clinically relevant educational materials that effectively utilize clinical data to meet brand objectives.Independently create scientific content through the analysis and interpretation of clinical data across various project types.Conduct comprehensive literature reviews, actively monitor the competitive landscape, and perform thorough competitive analyses.Build strong client relationships, contributing proactively in meetings and discussions.Collaborate with internal teams to craft engaging educational content and initiatives for healthcare professionals, including slide presentations and digital media.Work closely with creative teams to develop interactive programs that utilize scientific storytelling and innovative data visualization techniques.Collaborate in articulating the company's perspectives and recommendations to clients.Play a pivotal role in educating team members about disease states, clinical trials, treatments, and competitors.Assist in the preparation of materials for medical and regulatory approval processes, integrating client and regulatory feedback.Demonstrate a commitment to diversity, equity, and inclusion, fostering an inclusive workplace culture.Perform additional duties as assigned.