Role Description Maven is seeking a mission-driven, empathetic Clinical Dietitian (Diätassistent/in, Germany) to support members through virtual care services. As a Maven provider, you will have the opportunity to connect with members across the globe, expanding access to high-quality healthcare and creating meaningful impact at scale. You will join a curated provider network spanning 30+ specialties and 350+ subspecialties, focused on delivering holistic, high-value care. As we continue to grow our member base across 175+ countries, we are also expanding our best-in-class provider network. If you are passionate about improving clinical outcomes, reducing healthcare costs, and delivering compassionate, evidence-based care, you would be a strong addition to our team. What You'll Do: - Provide virtual care and support to adult members via 20-minute video consults and asynchronous messaging around: - Weight loss/weight gain concerns - Prenatal counseling - Gestational diabetes results and testing - Preparation for breastfeeding nutrition - Prenatal / Postpartum/ Fertility nutrition - Nausea/can't keep food down/how to reintroduce appetite - PCOS - Eating Disorders - Capture encounter summary documentation in our practice management system, MPractice - Collaborate with Maven’s Care Delivery team to ensure member needs are met, including recommendations for in-person referrals and follow-ups - Serve as an ambassador of Maven’s unique care model, providing culturally humble care and championing our belief that better outcomes for women and families mean a better world for everyone Qualifications - Must be a qualified Dietitian with valid German state certification/licensure (Diätassistent or equivalent recognized qualification) - Must be residing in Germany - Must be fluent in both English and German - Must be able to provide direct patient care for approximately 5 hours per week - This is a part-time, independent contractor role (1099 equivalent arrangement) - Minimum of 3 years’ experience in tele-health or digital health delivery - Comfortable providing care via a digital health platform and virtual consultations - Strong interest in women’s health and family health Opportunity Highlights - Flexibility: Meet with members virtually, when and where it’s convenient for you. - Expand your practice: Supplement your regular practice through Maven’s proprietary, secure telehealth platform: - Provide care via video and private messaging - Participate in unique opportunities, e.g. moderating community forums, leading virtual member classes, writing or reviewing educational articles - In-person referrals to your practice - Training & events: Optional participation in Maven sponsored lectures, panels, and/or other speaking opportunities as needed Benefits - The opportunity to connect with 30+ specialty types - A support system, including a Care Support Team, to answer your questions, handle paperwork, manage referrals and ensure continuity of care - The opportunity to serve Maven members around the globe, with language and care matching services - Membership in a world-class network of health and clinical experts across fields - We seek and embrace experts from all backgrounds, cultures, and communities to mirror and better care for our ever-growing member base.

Role Description The Global Clinical Lead is a significant subject matter expert (SME) role that exists within Telix to design, lead and implement the clinical development strategy for the Company’s Therapeutic assets. - Design, lead and implement Clinical Strategy: Define and drive the clinical development plans for Telix’s Therapeutic assets, ensuring alignment with Telix’s broader asset strategy and commercial objectives. - Cross-functional collaboration: Partner closely with Global Program Heads, Clinical Operations, Regulatory Affairs, Medical Affairs, and the Therapeutic Business Unit Head to ensure clinical trial objectives are integrated into the overall development strategy and reflect the needs of internal and relevant external stakeholders. - Clinical study design and execution: Oversee the development of clinical study plans from concept through to protocol finalization, ensuring scientific rigor and alignment with regulatory expectations, healthcare provider needs, patient advocacy perspectives, and market access requirements. - Clinical documentation leadership: Lead the creation and review of essential clinical documentation - including informed consent forms, imaging charters, study manuals, and regulatory dossiers - in collaboration with medical writers and cross-functional teams. - Regulatory and scientific contributions: Provide expert clinical input into key regulatory and scientific documents, including Investigator Brochures, IMPDs, DSURs, PSURs, SUSARs, Clinical Study Reports, and global regulatory submissions (e.g., INDs, BLAs, NDAs, MAAs). - Data integrity and analysis: Lead the review, interpretation, and quality control of clinical data, including efficacy, safety, and imaging endpoints, to ensure data integrity and support decision-making across the development lifecycle. - Stakeholder communication: Prepare and deliver high-impact presentations, proposals, and reports for senior leadership, external partners, and strategic collaborators to communicate program progress and clinical insights. - External engagement and thought leadership: Cultivate relationships with Key Opinion Leaders (KOLs), organize advisory boards, and collaborate with subject matter experts, consultants, and vendors to inform clinical strategy and enhance program visibility. Qualifications - Medical degree (MD/MBBS) is required. - Demonstrated experience in Oncology or Nuclear Medicine is required, with a strong understanding of the clinical and scientific landscape. - 5+ years of industry experience in clinical development, with a proven track record of leading clinical programs through early-phase development. Experience in early-stage clinical trial design and execution is strongly preferred. - Solid understanding of global clinical trial methodology, regulatory frameworks, and submission processes. Experience preparing and submitting regulatory documents (e.g., INDs, CTAs) and engaging with health authorities (e.g., FDA, EMA) is preferred. - Demonstrated success in leading cross-functional teams and managing complex clinical development programs from concept through execution. - Strong knowledge of clinical trial design, data interpretation, and the ability to translate scientific insights into strategic development plans. Key Capabilities - Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do. - Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results. - Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges. - Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language. - Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals. - Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges. - Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected. - Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges. - Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders. - Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills.

Role Description We're looking for a Biostatistician who is passionate about statistical methodology and thrives at the intersection of academic rigour and real-world software impact. You have a strong grounding in statistics and hands-on experience in biostatistics, clinical trials, or a closely related field — and you're energised by the challenge of translating cutting-edge research into tools used by the world's leading pharmaceutical and biotech companies. In this role you will get to: - Research and develop new statistical methods for inclusion in nQuery, spanning sample size determination, power analysis, adaptive design, Bayesian statistics, and clinical trial simulation. - Prototype and validate statistical methodologies in collaboration with our experienced in-house development team. - Support software users with statistical queries and guidance on the latest product enhancements. - Represent nQuery externally through online webinars, client training sessions, and high-impact industry conferences across Ireland/UK, EU, and US. - Write and record online content that helps communicate complex statistical concepts to a broad audience. Qualifications - 1–5 years of relevant experience in (bio)statistics, clinical trials, or data science/analysis. - PhD or MSc in Statistics/Biostatistics, or a BSc/BA with a specialisation in (Bio)Statistics. Requirements - Strong background and demonstrable interest in statistics. - Proficiency in R, with the ability to prototype and test statistical methodologies. - Solid understanding of clinical trial design concepts and statistical methodology. - Ability to communicate clearly with both technical and non-technical audiences. Benefits - Dynamic, remote-friendly environment that fosters high integrity and collaboration. - Opportunity to accelerate scientific progress and discovery.

Title: Forensic Psychologist - Clinical Supervisor Location: CA - Work Type: Remote, Full Time Job ID: 730517 Job Description: Psychologists are encouraged to consider an available Clinical Supervisor position with Liberty Healthcare’s multi-site forensic mental health program in California. This program exclusively serves justice-involved adults who are experiencing mental illness and have recently been determined to be incompetent to stand trial. The goal of this program is to provide rapid mental health services to people in need - so they may achieve improved behavioral health outcomes as quickly as possible. Services are provided onsite to inmates at several county jails in located in San Bernardino, Riverside, San Diego, and San Mateo Counties. As Liberty Healthcare’s Clinical Supervisor, you will enjoy an array of responsibilities, including: - Overseeing forensic evaluations for people who are justice involved and experiencing mental illness - Ensuring clinical services are consistent with best practices in the forensic mental health field - Leading various quality assurance, compliance, and training initiatives - Direct and indirect supervision of licensed clinicians and ancillary professionals - Collaborating with the program’s Executive Director as well as program leaders and staff - Fostering collaborative relationships with stakeholders at the California Department of State Hospitals and county sheriff’s departments - Providing clinical services occasionally as needed This is primarily a remote role which will allow you to work remotely from your home office in California. Although infrequent, you may be required to occasionally travel to service locations (mostly in Southern California). As a full-time employee of Liberty Healthcare in this role, you can expect: - Starting pay between $130,000 and $145,000 (depending on qualifications) - Health insurance, dental insurance, vision insurance, life insurance, and disability insurance - 30 days of paid time off each year for holidays, vacation, sick leave, and personal days - Health Savings Account, 401k plan, and other perks You are a good fit for this role if you possess the following: - Professional licensure in California as a Clinical Psychologist - At least two years of forensic mental health experience - Knowledge of best practices in the evaluation and treatment of justice involved people who are experiencing mental illness - Ability to lead others Although this is a remote position, California residency is required.