• Work within the Medical Affairs organization to identify, establish, and manage collaborative professional relationships with community-based scientific leaders (SLs) and healthcare providers. • Conduct peer-level scientific discussions and maintain a reliable presence to ensure SLs have a Medical Affairs contact within our company. • Engage in proactive non-product discussions regarding scientific issues to understand real-world prevention gaps, persistent disparities, and barriers to uptake across care settings • Facilitate appropriate scientific exchange of information with SLs, including integration of scientific knowledge with actionable insights to inform our Company's research, development and strategies. • Communicate external stakeholder opinions, insights, and feedback on new data, clinical trends, and the evolving HIV treatment and prevention landscape to Medical Affairs HQ teams. • Represent R&D at scientific meetings and congresses to understand the sentiment of the consumer and contribute to R&D debriefs, insight discussions, and post-congress reports. • Develop and execute territory plans in alignment with global Virology strategy. • Support data generation activities when requested by R&D leadership, including our company's Investigator Study Program (MISP). • Identify potential investigators for participation in phase II-IV clinical development programs and provide scientific support for R&D sponsored trials as needed. • Demonstrate and maintain in-depth knowledge of the assigned disease and therapeutic area(s) through educational efforts. • Fully comply with all company policies and applicable laws, regulations, and ethical standards.

Role Description Biolongeva es una plataforma B2B diseñada para ser el sistema operativo completo de las clínicas de longevidad modernas: integra IA clínica, generación de protocolos, verificación de contraindicaciones, herramientas para el paciente y fulfillment de péptidos de grado farmacéutico en un solo lugar. Xtnd Vida es su contraparte B2C, que entrega protocolos personalizados directamente al consumidor final a través de una red de afiliados. Esta posición fue creada para ser el eje clínico de ambos modelos. Como Experto(a) Médico en Longevidad de la compañía, esta persona será la autoridad clínica principal: responsable del rigor científico de los protocolos, la credibilidad del posicionamiento médico de la empresa y la calidad de la inteligencia clínica embebida en la plataforma. Este no es un cargo clínico-asistencial en el sentido tradicional. Es un rol estratégico que opera en la intersección de medicina, producto y ejecución comercial. El candidato idóneo tendrá conocimiento profundo en péptidos y medicina de longevidad, y traducirá ese conocimiento en protocolos, contenido, validación clínica y credibilidad frente a médicos y consumidores por igual. Qualifications - Título de médico (MD) o credencial clínica equivalente con licenciatura activa, O formación a nivel doctoral en un campo clínico o biomédico con expertise aplicado profundo en péptidos y medicina de longevidad. - Conocimiento especializado y demostrable en terapia con péptidos: GLP-1s, BPC-157, TB-500, secretagogos de hormona de crecimiento y compuestos relacionados — más allá de un conocimiento general. - Capacidad para diseñar protocolos clínicamente rigurosos y defender su razón científica tanto ante profesionales de la salud como ante audiencias no clínicas. - Comodidad operando en la intersección de medicina y negocio: esta persona interactuará con equipos comerciales, de producto y de liderazgo — no solo con personal clínico. Requirements - Diseñar, validar y actualizar protocolos personalizados de longevidad que incluyan péptidos, interpretación de biomarcadores, suplementación e intervenciones relacionadas. - Establecer y mantener estándares clínicos de calidad, gestión de contraindicaciones y seguridad en dosificación para ambos modelos. - Revisar y validar la lógica clínica de los outputs generados por la IA de Biolongeva, asegurando que los protocolos sean seguros, basados en evidencia y clínicamente sólidos. - Desarrollar marcos de protocolos estandarizados que puedan aplicarse de forma consistente en la plataforma y personalizarse por las clínicas afiliadas. - Ser el rostro clínico de Biolongeva en conversaciones con médicos, dueños de clínicas y equipos de salud, aportando la profundidad científica que genera confianza y cierra cuentas. - Apoyar el proceso comercial con expertise clínico: participar en demostraciones, responder preguntas técnicas y traducir las capacidades de la plataforma a lenguaje médico. - Construir y mantener relaciones con líderes de opinión y profesionales de la medicina de longevidad. - Desarrollar contenido clínico que posicione a la compañía como referente en longevidad y medicina de péptidos: guías clínicas, materiales educativos para afiliados y pacientes, y contenido de autoridad. - Revisar y validar toda comunicación externa que incluya afirmaciones clínicas, descripciones de protocolos o información científica. - Mantenerse al día en investigación emergente en péptidos, longevidad, hormesis, ciencia de biomarcadores y campos adyacentes, e incorporar hallazgos relevantes a la estrategia clínica y de producto. - Colaborar con el equipo de producto para mejorar continuamente la capa de IA clínica de Biolongeva: identificar brechas, proponer mejoras y validar nuevas funcionalidades. - Definir la arquitectura de datos clínicos para los protocolos de pacientes: qué se monitorea, cómo se mide el progreso y qué activa una revisión clínica. Benefits - Práctica clínica activa o red en longevidad, medicina funcional, antienvejecimiento o salud integrativa. - Experiencia previa en un rol de asesoría médica, asuntos médicos o liderazgo clínico dentro de una startup de salud, medtech o pharma. - Trayectoria en producción de contenido clínico: investigación publicada, materiales de educación médica o liderazgo de opinión reconocido en medicina de longevidad. - Familiaridad con interpretación de biomarcadores, análisis de laboratorio y marcos de medicina personalizada. - Experiencia con plataformas de salud digital o herramientas de IA clínica. - Bilingüe (español e inglés), relevante dado el alcance LATAM e internacional de la compañía.

Role Description Join our team at Fitchburg Comprehensive Treatment Center (CTC) as a Medical Director, where you'll play a pivotal role in transforming lives through exceptional care. In this role, you'll oversee medical and clinical practices, guide quality assurance, and provide direct patient care, all while working alongside a multidisciplinary team to uphold the highest standards of care. If you’re a compassionate physician with a commitment to excellence and a passion for behavioral health and substance use treatment, we invite you to lead and inspire at CTC. Responsibilities - Oversees and is responsible for the quality, efficiency and management of delivering medical services within the clinic. - Defines protocols and assists in decision making pertaining to the medical care of patients that is consistent with current medical practice and CTC policies and procedures. - Provides oversight to other professional medical staff, as well as administrative or support staff, as designated. - Serves as a liaison between the medical staff, other clinic staff, division or corporate staff, and organizational leadership. - Monitors assigned staff to adherence to established medical and clinic policy. - Provides back up call coverage. - Serves in a teaching capacity for the training and development of other personnel. - Responsible for securing physical exam and history from the patient, reviewing medical records, making medical evaluations, requesting appropriate diagnostic testing, prescribing medications and treatments, assisting in the management of behavioral or mental health problems of patients, maintaining current medical records in accordance with federal or state regulation, and clinic or corporate policies and procedures. - Performs other duties as assigned. - Encourages and builds mutual trust, respect and cooperation among team members. Qualifications - Doctoral degree in Medicine (MD or DO). - Prefer previous experience in behavioral health or substance use (SUD) treatment. - No history of alcohol or drug misuse for a period of three years before employment. - Current license to practice medicine by the state of Massachusetts. - Board certification or certificate of admissibility for board certification by American Society of Addiction Medicine (ASAM), American Academy of Addiction Psychiatry (AAAP), or other certification within their discipline. - Current DEA credentials to prescribe controlled substances without restrictions and per regulation within the state in which the practitioner will be working. - Additional specific DEA credentials may be required, per state and clinic regulations or policy. Compensation - Calculated Salary Range for the role: $165-$175 per hour.

Medical Science Liaison (MSL), CNS/Neuropsychiatry (Southeast) Location: GA, FL, NC, VA, TN, SC, KY, MS, AL, United States Job Description: Tagged: Nationwide, Medical Science Liaison, Medical Affairs, Clinical Trial Liaison, MSL, TMAC, Neuroscience, Clinical Research, Field Medical Medical Science Liaison (MSL), CNS/Neuropsychiatry (Southeast) Territory: Northeast, 50-70% travel Location: Home based anywhere in (GA, FL, NC, VA, TN, SC, KY, MS, AL) Business Unit: Medical Affairs Reports to: Senior Director, Field Clinical and Medical Programs, TMAC SUMMARY Serving as a field resource for the Company, the Medical Science Liaison (MSL) will support the company’s neurology/psychiatry Phase II clinical development pipeline. The MSL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators to support efforts to improve recruitment and activation timelines. The MSL will be responsible for developing and fostering relationships with key stakeholders including clinical investigators and site staff to represent the company with the goal of improving enrollment, expanding current therapeutic concepts, and achieving enrollment and retention goals. Duties and Responsibilities: - Strengthen the organization’s scientific presence and credibility in neuropsychiatric disorders, including schizophrenia and bipolar depression - Maintain deep clinical and scientific expertise within the neuropsychiatric area - Partner with investigators and site staff to support clinical trials, ensuring understanding of protocols and patient requirements - Identify and recommend new clinical trial sites; support feasibility, site selection, and site initiation activities - Provide consistent, compliant scientific support to investigators and site personnel - Identify barriers to trial execution and contribute solutions to enhance recruitment and retention - Act as a field-based scientific resource, addressing trial-related questions and challenges - Build and maintain relationships with key opinion leaders (KOLs) and healthcare professionals - Collaborate cross-functionally with medical affairs, clinical development, and operations teams - Respond to unsolicited medical information requests in a compliant manner - Support scientific meetings, advisory boards, and conference activities Qualifications: - Advanced degree (PharmD, PhD, MD, NP, PA) or equivalent terminal degree with appropriate clinical experience and scientific background required - 2+ years’ CNS/Neuropsychiatry clinical, academic and/or medical experience required - Prior experience as an MSL (3-6 years); preferably with a clinical trial focus in a pre-launch setting required - Proven ability to engage Investigators/KOLs in non-promotional, scientific exchange - Ability to travel, locally and regionally, up to 50% with overnight stays (car, plane, train) - Knowledge of local regulatory requirements and Pharmaceutical Association Codes, including regulations governing compliant scientific exchange - Demonstrated ability to integrate and work in cross functional network/matrix - Demonstrated project management ability The Medical Affairs Company (TMAC) has been the global provider of comprehensive clinical and medical staffing solutions for over 25 years. We specialize in the provision of field clinical and medical personnel based on our clients’ distinct resources and lifecycle needs. Clients in the biopharmaceutical, diagnostics, and medical device fields have turned to us to help manage their short- and long-term strategic and tactical clinical trial and medical engagement goals, aimed at providing support to numerous stakeholders including physicians, site staff, community practitioners, caregivers, and patients. Salary offers to be determined based on industry experience, education, and therapeutic expertise. #LI-JD1 #LI-Remote Salary Range $180,000 - $210,000 Job # 3693