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You will conduct comprehensive remote diagnostic assessments for autism and ADHD while collaborating with a multidisciplinary team to provide evidence-based clinical formulations. Additionally, you will deliver post-diagnostic support and feedback to clients and families to ensure they receive actionable information and appropriate care.
The Associate Director provides operational leadership for global clinical trial execution, overseeing vendor performance and cross-functional team collaboration. They are responsible for ensuring study delivery within budget and compliance with regulatory standards while managing clinical operations staff.
The Senior Clinical Trial Manager provides strategic leadership and operational oversight for complex global oncology clinical trials from start-up through closeout. They are responsible for managing CRO relationships, ensuring regulatory compliance, and driving patient enrollment and data quality strategies.
The Clinical Trial Manager II oversees all aspects of global clinical trial execution, including site selection, activation, and monitoring. They partner with CROs to ensure data quality, regulatory compliance, and adherence to study timelines and protocols.
The therapist will perform social services functions, including crisis intervention and family therapy, to assist patients in achieving optimal emotional health. They are also responsible for conducting therapeutic groups and coordinating with community agencies to provide comprehensive patient care.
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The Care Navigator manages a caseload of kidney health patients by coordinating care, performing health screenings, and maintaining member-centric care plans. They act as a liaison between patients, physicians, and support networks to ensure positive health outcomes and resolve care barriers.
The Pharmacy Care Coordinator assists with medication management, coordinates delivery, and provides telephonic support to patients for chronic disease management. They also manage patient orders, process insurance claims, and maintain accurate records while ensuring compliance with HIPAA regulations.
The Independent End Point Assessor will evaluate apprentices at the final stage of their healthcare training to ensure they meet industry standards. They will also record assessment data on the NCFE platform and participate in standardization events to maintain quality and consistency.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators to maintain high-quality clinical data and contribute to the preparation of study documentation.
The Clinical Application Specialist will support neurosurgical clinical programs by training personnel on the Neuro Exablate system and participating in brain indication treatments. They will also analyze treatment results, contribute to product development, and collaborate with regional teams to optimize the lifecycle of clinical centers.
The Telemedicine Physician will provide medical assessments and advice to subscribers via phone consultations. They are expected to manage general medicine cases and maintain a minimum productivity of 50 calls per 8-hour shift.
The manager is responsible for shaping and executing enterprise account strategies to build long-term, transformational partnerships with strategic healthcare customers. They will lead the full opportunity lifecycle, manage total account revenue, and drive cross-functional collaboration to deliver integrated medical solutions.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, maintain study documentation, and ensure compliance with ICH GCP and regulatory requirements.
The physician will perform clinical review and quality assurance for AI-driven patient-to-trial matching by validating clinical data against medical records. Additionally, they will represent the company in high-level meetings with pharmaceutical partners and industry stakeholders.
You will build trusted relationships with customers across South Africa to provide clinical education and technical guidance on prosthetic and orthotic solutions. The role involves conducting customer visits, workshops, and clinical discussions to improve patient outcomes.
The Medical Director will serve as the primary clinical voice for provider engagement, leading peer-to-peer conversations and resolving clinical-policy objections. They will also oversee clinical governance, including sign-off on protocols, drug list strategy, and representing the company to external stakeholders.
The Clinical Research Associate II will contribute to the development of therapies by supporting clinical trials and regulatory processes. They will work to improve global health outcomes through the delivery of clinical development solutions.
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The Executive Assistant will provide direct support to founders by managing calendars, coordinating meetings with international stakeholders, and handling sensitive documentation. They will also conduct research, maintain Notion records, and assist with financial and administrative tasks.
The Regional Clinical Manager will support the commercial success of neurorehabilitation technology by providing clinical education, product demonstrations, and training to healthcare professionals. This role acts as a clinical liaison during evaluations and site visits to ensure seamless onboarding and therapy adoption.
The Principal IT Trainer designs, develops, and maintains comprehensive Epic Cadence and HIM training materials, including instructor-led, virtual, and eLearning content. They also provide leadership in curriculum strategy, mentor other trainers, and act as a subject matter expert for system workflows.
The Senior CRA is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCP and regulatory standards. They also provide mentoring to less experienced staff, coordinate global study activities, and ensure the quality and timely submission of clinical data.
The Clinical Trial Manager serves as the primary point of contact for clinical studies, overseeing operational execution, site feasibility, and regulatory compliance. They are responsible for managing study budgets, developing clinical documentation, and leading internal teams to ensure study timelines and quality deliverables are met.
The Clinical Trial Manager serves as the primary point of contact for clinical studies, overseeing operational planning, conduct, and regulatory compliance. They are responsible for managing site feasibility, recruitment strategies, clinical monitoring, and ensuring data quality throughout the study lifecycle.
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Provide episodic non-emergency care to patients via remote appointments. Deliver digital-first, integrated healthcare services to private clients and employees.
The Clinical Research Associate acts as the primary site contact and manager, ensuring study conduct aligns with ICH-GCP, local regulations, and company quality standards. They are responsible for site monitoring, data integrity, and managing regulatory documentation throughout all phases of clinical research studies.
The role involves coordinating medication prior authorizations with insurance providers and supporting the billing department with patient accounts. You will also provide administrative support while ensuring strict adherence to HIPAA regulations.
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