Medical Director Remote Jobs in New Mexico (US)
This page tracks remote medical director openings that are location-eligible for New Mexico.
This page tracks remote medical director openings that are location-eligible for New Mexico.
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GSK é uma empresa biofarmacêutica global com o propósito de unir ciência, tecnologia e talento para enfrentar doenças juntos. Nossos objetivos incluem: Impactar positivamente a saúde de 2,5 bilhões de pessoas até o final da década. Prevenir e tratar doenças com inovação em medicamentos especializados e vacinas. Focar em quatro áreas terapêuticas: respiratória, imunologia e inflamação; oncologia; HIV; e doenças infecciosas. Estamos comprometidos em criar um ambiente onde nossos colaboradores possam prosperar e focar no que realmente importa.
Role Description The Thought Leader Liaison (TLL) builds and manages strategic relationships with a select group of U.S. external experts within assigned therapeutic areas across specialty groups to generate timely, actionable insights that inform brand strategy. The TLL plans and coordinates insight generation through ongoing interactions with external experts, congresses, and executive engagements, working closely with commercial, medical, and regulatory partners while maintaining executive presence and strict adherence to compliance requirements. Hepatology TLLs will play a critical role in the launch of hepatology drugs, developing expertise in quantitative HBsAg testing to identify target patients and accelerate adoption of a functional cure paradigm in Hepatitis B across their geographies. Key Responsibilities - External Expert Engagement & Relationship Management - Develop and maintain strategic relationships with assigned External Experts through meaningful, value-driven interactions. - Plan and execute compliant External Expert engagements aligned to brand priorities and External Expert needs outside of advisory and congress events. - Segment and manage a thought leader network to optimize engagement and insight generation. - Insight Generation & Strategic Impact - Compliantly elicit, document, and synthesize clinical, competitive, and strategic insights from External Experts. - Share insights with marketing senior leadership to inform brand strategy, resource allocation, and tactic development. - Seek compliant External Expert feedback on initiatives and materials. - Advisory, Peer to Peer & Congress Engagements - Plan and execute External Expert consulting engagements and advisory boards. - Coordinate and support External Expert executive interactions with commercial leadership. - Enable peer-to-peer education through speaker recommendations, development, training/operations support, and relationship management. - Lead sponsorship initiatives at Tier 1 congresses and serve as onsite host for product theater speakers and EE guests. - Cross-Functional & Operational Excellence - Partner effectively with medical, legal, compliance, regulatory, and marketing teams. - Apply strong project management skills to manage multiple priorities simultaneously. - Manage agency and vendor partners to ensure timely, high-quality execution. - Understand risk associated with the activities on Strategic Engagement and be adept and agile in their management and mitigation. Qualifications - Bachelor’s degree. - Minimum 10 years of experience in field sales, product marketing, or medical/clinical roles within pharma or biotech. - Specialty Hepatology/GI experience required in one of the above functions. - Experience presenting to executive audiences (live and virtual) and influencing strategic decisions or stakeholder alignment. - Experience leveraging insights to guide strategy development and proactively refine approach in response to evolving data and market dynamics. - Valid driver’s license. - Willingness to travel 60–80%, including nights and weekends. Preferred Qualifications - Master’s degree. - Strong account management and cross-functional leadership experience. - Marketing and/or sales management background. - Advanced project management and organizational skills. - Proven adherence to regulatory and compliance standards with proactive risk identification and mitigation. Benefits - Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
CVS Health is a leading healthcare company operating CVS Specialty, CVS Pharmacy, CVS MinuteClinic, and CVS Caremark. In 2018, CVS combined forces with healthca
Title: Medical Director -Spine Location: United States Job Description: Position Summary Aetna, a CVS Health Company, a Fortune 6 company, is one of the oldest and largest national insurers. That experience gives us a unique opportunity to help transform health care. We believe that a better care system is more transparent and consumer-focused, and it recognizes physicians for their clinical quality and effective use of health care resources. **This is a remote based (work at home) based anywhere in the US.** Aetna, a CVS Health Company, has an exciting opportunity for a Medical Director (Spine) that can be remote based, work from home. The Medical Director (Spine) will be a Subject Matter Expert (SME) with a background in Orthopedic Spine OR Neurosurgery, including post-graduate direct patient care experience specifically. Expands Aetna's medical management programs to address member needs across the continuum of care. Supports the Medical Management staff ensuring timely and consistent responses to members and providers. Leads all aspects of utilization review/quality assurance, directing case management Provides clinical expertise and business direction in support of medical management programs through participation in clinical team activities. Acts as lead business and clinical liaison to network providers and facilities to support the effective execution of medical services programs by the clinical teams. Responsible for predetermination reviews ad reviews of claim determinations, providing clinical, coding, and reimbursement expertise, using multiple computer based applications. Required Qualifications * 2 or more years of experience in Health Care Delivery System e.g., Clinical Practice and Health Care Industry. * Active and current state medical license without encumbrances. * M.D. or D.O., Board Certification in a Orthopedic Spine OR Neurosurgery, including post-graduate direct patient care experience specifically. Preferred Qualifications * Previous healthcare insurance experience. Education * 2 or more years of experience in Health Care Delivery System e.g., Clinical Practice and Health Care Industry. * Active and current state medical license without encumbrances. * M.D. or D.O., Board Certification in a Orthopedic Spine OR Neurosurgery, including post-graduate direct patient care experience. Pay Range The typical pay range for this role is: $174,070.00 - $374,920.00 This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, geography and other relevant factors. This position is eligible for a CVS Health bonus, commission or short-term incentive program in addition to the base pay range listed above. This position also includes an award target in the company’s equity award program. Our people fuel our future. Our teams reflect the customers, patients, members and communities we serve and we are committed to fostering a workplace where every colleague feels valued and that they belong.
• Leads the operational backbone of the US/CAN Medical Affairs. • Ensures compliant, efficient, and high‑quality execution of medical strategies across the PDx portfolio. • Manages a team and partners closely with Medical Affairs, Patient Safety, Regulatory, Quality, Compliance, Clinical Applications team and Commercial colleagues. • Drives operational planning cycles including medical activity tracking, dashboards, KPIs, and compliance documentation. • Translates scientific and medical priorities into executable operational processes, systems, and workflows.
Role Description This on-site, contract position offers an exceptional opportunity to deliver high-quality telehealth services while contributing to our mission of providing comprehensive medical care in a supportive environment. As a Locum MD in Endocrinology, you will play a crucial role in diagnosing and managing endocrine disorders through virtual consultations. You'll work collaboratively with our multidisciplinary team to enhance patient outcomes and ensure a seamless telehealth experience. - Conduct telehealth consultations for patients with endocrine disorders - Diagnose, treat, and manage chronic endocrine conditions - Develop and implement individualized treatment plans - Collaborate with healthcare professionals to coordinate patient care - Document patient interactions and maintain medical records - Educate patients on disease management and lifestyle modifications - Participate in case discussions and clinical meetings - Stay updated with advancements in endocrinology and telemedicine Qualifications - MD degree from an accredited medical school - Board-certified in Endocrinology - 1-3 years of clinical experience in endocrinology - Strong understanding of telehealth technologies and practices - Excellent communication and interpersonal skills - Ability to work collaboratively in a team-oriented environment - Strong organizational skills and attention to detail - Current medical licensing in relevant states Requirements - Flexible Schedule: 10-12 hours per week - No call required - Setting: 100% Remote - Case Types: Bread and butter endo cases, testosterone therapy, ED, hair loss, general wellness, diabetes, and mostly controlled substances - New Patient Appointments: 15-30 minutes - DEA required - Must be board-certified or board-eligible
Waters Corporation (NYSE:WAT) is a global leader in life sciences and diagnostics, dedicated to accelerating the benefits of pioneering science through analytical technologies, informatics, and service. With a focus on regulated, high-volume testing environments, our innovative portfolio harnesses deep scientific expertise across chemistry, physics, and biology. We collaborate with customers around the world to advance the release of effective, high-quality medicines, ensure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combating antibiotic resistance. Through a shared culture of relentless innovation, our passionate team of ~16,000 colleagues turn scientific challenges into breakthroughs that improve lives worldwide. Diversity and inclusion are fundamental to our core values at Waters Corporation. It benefits our employees, our products, our customers, and our community. Waters complies with all applicable federal, state, and local laws. Qualified applicants are considered without regard to sex, race, color, ancestry, national origin, citizenship status, religion, age, marital status (including civil unions), military service, veteran status, pregnancy (including childbirth and related medical conditions), genetic information, sexual orientation, gender identity, legally recognized disability, domestic violence victim status, or any other characteristic protected by law. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. All hiring decisions are based solely on qualifications, merit, and business needs at the time.
Role Description Waters Advanced Diagnostics is seeking a Director, Medical Affairs, to provide strategic and scientific leadership across the Medical Affairs function. This role will help shape how clinical, scientific, and market insights inform product strategy across microbiology, molecular, point-of-care, and other high-value diagnostic workflows in regulated clinical settings. The Director serves as a senior Medical Affairs representative, partnering closely with Research and Development, Clinical Affairs, Regulatory, Quality, Commercial, and other cross-functional leaders. This individual translates unmet customer and patient needs, evolving clinical practice, and real-world evidence into actionable medical strategies that strengthen product differentiation, support lifecycle decisions, and enable successful development and adoption of innovative diagnostic solutions. This role leads new product development and product lifecycle management, while guiding scalable, data-driven, and AI-enabled approaches to planning, execution, and performance management. The Director is expected to bring deep diagnostic and laboratory expertise, strong business acumen, and a collaborative leadership style to advance medical credibility, innovation, and patient impact across Waters Advanced Diagnostics. Responsibilities - Lead Medical Affairs strategy and execution for the Advanced Diagnostics Division - Collaborate with cross-functional teams, including R&D, marketing, sales, and regulatory, to ensure a cohesive and integrated approach to medical affairs. - Identify evidence gaps and contribute to real‑world evidence, clinical research, and publication strategies in partnership with marketing and R&D teams. - Serve as a scientific advisor for internal teams and external stakeholders. - Stay up to date on industry trends, market dynamics, and competitor activities to inform the development of innovative strategies and initiatives. - Partner with laboratory medicine organizations and serve as a thought leader, representing the company at conferences, events, and with key opinion leaders. - Provide strategic input and guidance to product development teams to ensure the company's portfolio meets the needs of healthcare professionals and patients. - Lead the adoption of AI-enabled tools to improve operational efficiency, reporting, and workflow management - Guide teams in effectively leveraging AI tools, acting as a resource for adoption and best practices - Establish and evolve key metrics to measure Medical Affairs performance and impact - Translate complex medical/scientific data into actionable business insights. - Foster a culture of collaboration, innovation, and continuous learning within the medical affairs team and across the organization. - Act as a mentor and coach to team members, providing guidance and support in their professional development and growth. Qualifications - Advanced medical or scientific degree in the life sciences or related field - 10+ years of experience as Director of a Clinical Microbiology Laboratory or equivalent leadership roles in laboratory medicine, infectious disease diagnostics, or precision medicine environments preferred. - Demonstrated leadership and team management experience - In-depth knowledge of newly developing technology in the field of infectious diseases diagnostics, scientific study design and implementation, as well as data analysis of study findings. - Extensive experience conducting and publishing scientific studies in the field of Clinical Microbiology and Infectious Diseases. - High credibility with internal stakeholders and external clinical experts. - Exposure to Medical Affairs, product development, or cross-functional team environments preferred. - Ability to work remotely (U.S.) with some limited travel Company Description Waters Corporation (NYSE:WAT) is a global leader in analytical instruments, separations technologies, and software, serving the life, materials, food, and environmental sciences for over 65 years. Our Company helps ensure the efficacy of medicines, the safety of food and the purity of water, and the quality and sustainability of products used every day. In over 100 countries, our 7,600+ passionate employees collaborate with customers in laboratories, manufacturing sites, and hospitals to accelerate the benefits of pioneering science. Diversity and inclusion are fundamental to our core values at Waters Corporation. It benefits our employees, our products, our customers and our community. Waters complies with all applicable federal, state, and local laws. Qualified applicants are considered without regard to sex, race, color, ancestry, national origin, citizenship status, religion, age, marital status (including civil unions), military service, veteran status, pregnancy (including childbirth and related medical conditions), genetic information, sexual orientation, gender identity, legally recognized disability, domestic violence victim status, or any other characteristic protected by law. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. All hiring decisions are based solely on qualifications, merit, and business needs at the time.
• Serve as Clinical Operations Expert across PSI opportunities • Provide oversight to ensure clinical accuracy, alignment with best practices, and evidence-based recommendations • Function as rural health subject matter expert, helping design and adapt solutions • Provide test subject matter expertise to achieve validation of design acceptability criteria • Support solutioning for program of government customers’ needs in implementing/integrating rural health applications • Develop, implement and sustain clinical solutions for PSI’s Emerging Technology and Innovation activities • Serve as Clinical Operations Leader across PSI • Provide thought leadership to strengthen PSI’s market positioning • Mentor PSI staff and partners to integrate clinical excellence into operations, development, and delivery models
Role Description This position is located in the Health Information Management (HIM) section at the Phoenix VA Medical Center. Medical Records Technicians (Coder-Outpatient) are skilled in classifying medical data from patient health records in the hospital setting, and/or physician-based settings, such as physician offices, group practices, multi-specialty clinics, and specialty centers. They analyze and abstract patients' health records, and assign alpha-numeric codes for each diagnosis and procedure. Responsibilities - Utilizes computer applications with varied functions to produce a wide range of reports, to abstract records, and review assigned codes. - Performs audits of encounters to identify areas of noncompliance in coding. - Facilitates improved overall quality, completeness, and accuracy of coded data. - Works with staff to ensure that regulations are met, or areas of weakness are identified and reported to the appropriate supervisor for corrective action. - Selects and assigns codes from the current version of several coding systems, including the current versions of the International Classification of Diseases (ICD), Current Procedural Terminology (CPT), and/or Healthcare Common Procedure Coding System (HCPCS). - Adheres to accepted coding practices, guidelines, and conventions when choosing the most appropriate diagnosis, operation, procedure, ancillary, or Evaluation and Management code to ensure ethical, accurate, and complete coding. - Searches the patient record to find documentation justifying code assignment based on an expanded knowledge of the organization and the structure of the patient health record. - Responsible for performing audits of coded data, developing criteria, collecting data, graphing and analyzing results, and creating reports and communicating in writing and/or in person to appropriate leadership and groups. - Maintains statistical databases to track the results and validate the program for identifying patterns and variations in coding practices, with regular reports to the medical staff and management. Work Schedule Hours to be discussed during the interview process. Remote These approved positions are currently designated for a mid-term extension to the return to office mandate through October 2025. While these positions may be filled remotely, the employee will be required to return to the office if the mid-term extension is not continued. Therefore, all applicants must be located within 50 miles of a VA facility. Telework This position is telework eligible but may be required to return to the office permanently at a later date. Qualifications - Applicants pending the completion of educational or certification/licensure requirements may be referred and tentatively selected but may not be hired until all requirements are met. - United States Citizenship: Non-citizens may only be appointed when it is not possible to recruit qualified citizens in accordance with VA Policy. - Experience: One year of creditable experience that indicates knowledge of medical terminology, anatomy, physiology, pathophysiology, medical coding, and the structure and format of a health records. - Education: An associate's degree from an accredited college or university recognized by the U.S. Department of Education with a major field of study in health information technology/health information management, or a related degree with a minimum of 12 semester hours in health information technology/health information management. - Completion of an AHIMA approved coding program, or other intense coding training program of approximately one year or more that included courses in anatomy and physiology, medical terminology, basic ICD diagnostic/procedural, and basic CPT coding. - Certification: Persons hired or reassigned to MRT (Coder) positions in the GS-0675 series in VHA must have either Apprentice/Associate Level Certification, Mastery Level Certification, or Clinical Documentation Improvement Certification through AHIMA or ACDIS. - English Language Proficiency: MRTs (Coder) must be proficient in spoken and written English as required by 38 U.S.C. § 7403(f). Requirements - Ability to analyze the health record to identify all pertinent diagnoses and procedures for coding and to evaluate the adequacy of the documentation. - Ability to accurately perform the full scope of outpatient coding, including ambulatory surgical cases, diagnostic studies and procedures, and outpatient encounters. - Skill in interpreting and adapting health information guidelines that are not completely applicable to the work, or have gaps in specificity. Physical Requirements They analyze and abstract patients' health records, and assign alpha-numeric codes for each diagnosis and procedure.
CommonSpirit Health is a nonprofit organization that is on a mission to improve people’s health while making “the healing presence of God known.” The orga
Role Description As our Medical Receptionist, you will be the essential first point of contact for patients and visitors within our specialized Palliative Care practice, embodying the compassionate and welcoming spirit of our service. You will play a pivotal role in patient registration, appointment scheduling, and insurance verification, ensuring a seamless and supportive administrative experience. - Warmly greet patients and visitors. - Manage the reception area. - Handle multi-line phone calls with a pleasant and helpful demeanor. - Meticulously register new patients in IDX. - Accurately verify insurance eligibility and benefits. - Update patient demographic and financial information. - Perform various clerical duties, including: - Maintain departmental deposit logs. - Prepare routine schedules and reports. - Utilize analytical skills necessary to maintain provider schedules. - Ensure a positive customer service atmosphere and interactions in reception areas. - Oversee the waiting area. - Coordinate patient movement and report problems or irregularities. - Possess a working knowledge of multi-line phones. Qualifications - High school diploma or GED. - Strong basic computer skills, including proficiency with Outlook, Windows-based, and Google Suite programs. - Exceptional ability to communicate effectively. - Ability to multitask and maintain professional working relationships with patients, employees, and physicians. Requirements - High School Graduate/GED. - Basic computer skills. - Google Suites based programs. Benefits - Opportunity to grow within a comprehensive network of inpatient and outpatient services. - Access to a vibrant community hospital and leading regional healthcare system. - Experience a charming blend of bygone appeal and modern amenities in Prescott. - Enjoy a relaxed lifestyle that empowers professional growth and family time.
Founded in 2004 and led by CEO Steve Chapman, Natera is a company in the biotechnology market that offers genetic testing and diagnostics on a global scale. Ope
• Partner with the Sr. Medical Director, Oncology on the clinical development of cell-free DNA (cfDNA) molecular diagnostics and liquid biopsy assays for gynecologic cancers • Direct the development and execution of clinical strategies and evidence-generation plans that demonstrate clinical utility in gynecologic oncology, including minimal residual disease (MRD) tracking, recurrence monitoring, treatment response assessment, and clinical trial enrichment • Oversee medical education and scientific communications for healthcare providers focused on gynecologic oncology, including tumor boards, webinars, and field medical enablement • Partner with commercial and marketing teams to deliver clear, data-driven clinical evidence and educational materials to gynecologic oncology stakeholders • Represent Natera at medical congresses and industry events, including SGO, ASCO, and ESMO, both in person and virtually • Build and maintain relationships with external experts, clinical investigators, cooperative groups such as NRG/GOG, and professional societies within gynecologic oncology • Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development, endpoint selection, data analysis, data interpretation, peer-reviewed publications, and congress submissions in gynecologic oncology
Role Description The Chief Medical Officer (CMO) serves as the senior clinical executive for OnePeak Medical, responsible for providing strategic clinical oversight and ensuring regulatory, payer, and quality compliance. The CMO oversees quality programs, provides medical direction and supervision to the provider team, and partners with leadership to safeguard the highest standards of patient-centered care. This role may include limited direct patient care (not to exceed one day per week) to maintain clinical relevance and connection to frontline practice. Responsibilities and Duties - Clinical Governance & Oversight - Oversee and maintain clinical protocols aligned with OnePeak principles, evidence-based standards, and payer compliance. - Provide medical direction, supervision, disciplinary action, and support to providers or the Clinical Director as needed. - Ensure quality of care, adherence to medical necessity, and compliance with regulatory requirements (HIPAA, OSHA, payer rules). - Monitor coding, billing, and contracting practices to reduce audit and reimbursement risk. - Keep clinical policies and procedures current with best clinical and regulatory practices. - Serve as a subject matter expert in primary care, functional medicine, and hormone optimization. - Remain accessible for urgent clinical questions and complex case consultations. - Collaborate with the Clinical Director and leadership to: - Set provider performance expectations and productivity/quality goals. - Recruit, interview, and onboard providers. - Coach, evaluate, and develop improvement plans for clinical staff. - Plan and deliver provider training. - Quality, Safety & Outcomes - Lead organizational quality programs, including patient safety, satisfaction, and clinical outcomes reporting. - Champion adoption of evidence-based guidelines and standard operating procedures (SOPs). - Monitor provider adherence to documentation, coding, and utilization standards. - Drive continuous improvement initiatives to meet payer expectations and strengthen OnePeak’s standing in value-based care arrangements. - Participate in peer review, incident review, and adverse event mitigation activities. - Strategic & Administrative Duties - Participate in strategic and annual planning, including budget development for medical activities. - Represent OnePeak Medical’s clinical team in external meetings and community initiatives. - Partner with Operations to integrate new services and therapies safely and compliantly. - Coordinate care with referring physicians and oversee specialty or advanced care integration. - Perform additional administrative duties as assigned, including committee participation and operational planning. - Collaboration & External Relations - Serve as the clinical spokesperson for the organization with payors, regulators, and external stakeholders. - Partner with Marketing and Business Development to ensure clinically accurate and compliant communications. - Build external relationships with industry leaders, research organizations, and medical associations to support thought leadership and innovation. Qualifications - MD or DO, with active Oregon medical license (or eligibility). - Board certification in primary care, family medicine, internal medicine, or a relevant specialty. - Minimum 10-15 years of clinical practice with at least 5 years in a leadership role. - Proven experience overseeing quality programs, provider supervision, and regulatory compliance in a multi-site healthcare organization. - Strong knowledge of functional medicine, integrative care models, and payer expectations. - Excellent leadership, communication, and change management skills. Benefits - Medical, Dental, Vision, and Life Insurance - 401(k) Retirement Plan with Company Match - Voluntary LTD, FSA, Accident, Critical Illness - Paid Time Off and Paid Holidays - Employee and Family Discounts - Paid Parental Leave
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