Medical Director of Oncology

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 oncolo…

Munson Healthcare seeks a Medical Business Associate to join the gynecological oncology team in Traverse City. This position centers on supporting essential administrative and business functions for the department. Key responsibilities Handle daily administrative tasks to ensure efficient clinic operations Support the team with business processes that contribute to patient care quality Role focus This role helps maintain smooth workflow and consistent service standards for patients and staff within gynecological oncology.

About Nucs AINucs AI is at the forefront of transforming cancer care using advanced AI and medical imaging technologies. Established in 2024 by a diverse team of oncologists, AI experts, and healthcare innovators, we are addressing one of the most critical challenges in medicine: the increasing need for precise and timely cancer diagnostics amidst the surge in scan volumes and the shortage of radiologists.Our work lies at the junction of diagnostics and treatment planning, developing AI-driven tools that integrate medical imaging, radioligand therapy, and artificial intelligence. We are initially focusing on prostate cancer, with plans to broaden our impact across oncology by collaborating with leading medical institutions and pharmaceutical companies in the US, Europe, and Australia, aiming to incorporate precision oncology into routine clinical practice.Our mission is to enhance diagnostic accuracy and improve access to expert cancer care, ultimately elevating patient outcomes globally. As a venture-backed, early-stage company, we are assembling a team that combines profound clinical knowledge with engineering expertise—operating with the precision required by the medical field while responding swiftly to pressing problems.The OpportunityNucs AI is establishing a robust medical programs function to bolster our growing portfolio of clinical collaborations, validation studies, and regulatory evidence generation. This innovative role will be responsible for overseeing the operational execution of our medical programs—from clinical study coordination and site management to data collection, protocol adherence, and interdepartmental collaboration.You will serve as the operational backbone of the medical team, ensuring that clinical initiatives progress on schedule and meet specified criteria. Collaborating closely with the Medical Director, Chief Medical Officer, and Medical Affairs Lead, you will convert clinical strategies into actionable programs—managing timelines, liaising with clinical sites, supervising data workflows, and assisting with regulatory documentation.This position is ideal for individuals with a background in clinical operations who excel in dynamic, cross-functional environments and wish to play a pivotal role in how a clinical-stage AI enterprise delivers evidence and builds credibility within the medical community.

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 licenses, extensive experience as a Medical Director, a strong understanding of Workers’ Compensation laws across the United States, and familiarity with various state Workers’ Compensation treatment guidelines.Key responsibilities include conducting examinations in compliance with Washington State regulations, as well as being licensed and approved by Labor and Industries in Washington.This is a part-time position, with an expected workload of no more than 10 hours per month.Dane Street thrives on the contributions of each team member. We are committed to fostering a positive workplace that prioritizes client satisfaction and collaborative success.

Jobgether is hiring a Director of Cancer Research based in the US. This leadership position guides oncology research efforts, with a focus on advancing new approaches to cancer treatment and prevention. Role overview The Director of Cancer Research oversees research programs and manages teams of scientists working on oncology projects. Collaboration with industry partners is a key part of this role, helping to move scientific discoveries toward real-world applications. What you will do Lead and coordinate cancer research initiatives Supervise and support multidisciplinary research teams Work closely with external partners to drive progress in cancer treatment and prevention Requirements Extensive background in oncology research Demonstrated success managing complex research projects Experience leading and motivating scientific teams This role supports Jobgether’s mission to improve patient outcomes and contribute to scientific advances in cancer research.

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.

About UsDLH Corporation is dedicated to enhancing health and national security readiness through innovative solutions in scientific research, systems engineering, and digital transformation. Our team of experts in public health and operational performance works tirelessly to address the complex challenges faced by both civilian and military sectors. By leveraging cutting-edge tools such as artificial intelligence, data analytics, and cloud technologies, we strive to improve the lives of millions. With a workforce of over 2,400 professionals committed to the principle that 'Your Mission is Our Passion,' DLH combines extensive government sector experience with proven methodologies and a steadfast commitment to innovation. OverviewDLH is actively seeking a visionary Project Director to lead a significant federally funded cohort study focused on understanding environmental and genetic risk factors for cancer and other chronic diseases. The Project Director will be responsible for comprehensive contract execution, leading multidisciplinary teams, and collaborating with government Principal Investigators. This role encompasses overseeing complex, protocol-driven research activities, including participant engagement, biospecimen management, data operations, and outcome validation. The ideal candidate will possess a balance of executive project management skills and epidemiologic expertise, driving strategic study initiatives and operational excellence throughout all research phases. Additionally, the Project Director should have a well-established professional network and the strategic insight to identify and secure new contract opportunities that broaden our public health research endeavors.

Location: Remote with approximately 50% domestic and international travelJoin Natera in shaping the future of cancer care by taking on the pivotal role of Medical Director for Skin/Immuno-Oncology. This strategic leadership position will allow you to provide invaluable medical expertise and scientific guidance across our oncology portfolio, focusing on melanoma, cutaneous malignancies, and immunotherapy applications for solid tumors. Collaborate with diverse teams in research, development, medical affairs, and commercial functions to uphold the scientific integrity and clinical adoption of Natera’s innovative oncology testing solutions.Primary Responsibilities:Clinical Adoption:Lead the clinical strategy and evidence generation for melanoma, non-melanoma skin cancers, and pan-tumor immunotherapy indications.Work closely with clinical development, medical affairs, and commercial teams to translate emerging evidence into impactful clinical practice applications.Engage with key opinion leaders (KOLs), cooperative groups, and academic investigators to validate and expand clinical use cases for ctDNA-based diagnostics in immuno-oncology.Provide field-facing education and strategic guidance to healthcare providers, payers, and advocacy organizations regarding the clinical utility, interpretation, and impact of Minimal Residual Disease (MRD) and response monitoring in immune-treated populations.Identify and tackle barriers to adoption by aligning evidence generation, messaging, and stakeholder engagement with evolving standards of care and health system needs.Medical Education and Communication:Act as the medical and scientific spokesperson for skin and immuno-oncology programs, effectively communicating clinical utility, study data, and product value to external experts and stakeholders.Collaborate with commercial teams to create educational resources, medical content, and scientific training for healthcare providers and internal teams.Provide scientific leadership during advisory boards, symposia, and investigator meetings.Representation and Advocacy:Represent Natera at national and international oncology and immunotherapy conferences, building relationships with key opinion leaders in melanoma and immuno-oncology.

Revolution Medicines, Inc. is seeking a visionary and experienced Senior Director of Cancer Immunology to lead our research and development efforts in immunotherapy. This role will be pivotal in driving innovative strategies and groundbreaking therapies for cancer treatment.The ideal candidate will have a profound understanding of cancer immunology, a proven track record in drug development, and the ability to lead multidisciplinary teams. You will be responsible for formulating and executing research strategies, collaborating with cross-functional teams, and presenting findings to stakeholders.

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.

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

BridgeBio Pharma, Inc. is looking for an Associate Director of Medical Affairs to join the team remotely from anywhere in the USA. This position supports ML Bio Solutions, a BridgeBio company dedicated to developing BBP-418, a potential first oral treatment for patients with Limb Girdle Muscular Dystrophy type 2I/R9 (FKRP-related). Role overview This role focuses on supporting the development, coordination, and execution of strategic medical initiatives within medical affairs. The Associate Director will play a key part in advancing projects that aim to address unmet medical needs, particularly for rare diseases. About BridgeBio BridgeBio brings together innovative projects and early-stage academic research under one financial structure to minimize risk and accelerate progress. The company values curiosity, experimentation, and the responsible use of new technologies, including AI, to improve clarity and efficiency. Teams at BridgeBio are encouraged to challenge the status quo and work collaboratively to find solutions for patients with rare diseases. Key responsibilities Support the development and execution of medical affairs strategies for ML Bio Solutions. Coordinate strategic medical initiatives related to BBP-418 for LGMD2I/R9. Collaborate with cross-functional teams to advance medical projects and initiatives.

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.