Responsible for ingesting, validating, and operationalizing clinical data feeds from EDC, CTMS, and vendors into review platforms. The role involves building reusable ingestion frameworks and managing downstream exports for analytics and programming teams.
Remote Healthcare Jobs (12,430)
Job category = Healthcare
Provide end-to-end statistical support for the design, analysis, and reporting of IVD molecular assays for regulatory submissions. Act as the primary point of contact for regulatory questions and author statistical sections for clinical protocols and reports.
Director, Clinical Interoperability & Interfaces
CareMore Health
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Full Time
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3 Days Ago
CareMore Health
Lead the design and execution of enterprise-wide interoperability strategies to ensure secure health data exchange across systems. Oversee the implementation of interfaces and APIs while managing high-performing technical teams and vendor relationships.
Act as the first point of contact for users on a 24/7 on-call line to provide immediate emotional support and guidance. Document interactions and hand over critical cases to the day team following established protocols.
Provide immediate emotional support and guidance to users via a 24/7 on-call line outside of standard office hours. Document interactions and hand over critical cases to the daytime team following established protocols.
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Provide quality care and coordination for members through telephonic outreach and the development of individualized care plans. Collaborate with interdisciplinary teams to close treatment gaps and provide health education and community referrals.
Experienced Clinical Trial Coordinator (m/w/d), Home Office in Germany
IQVIA
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Full Time
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3 Days Ago
IQVIA
The role involves managing clinical trial documentation, maintaining the Trial Master File, and coordinating communication between research sites and internal departments. Additionally, the coordinator will mentor junior staff and assist with the distribution of clinical trial supplies.
Lead health technology assessment and economic evidence generation projects to secure market access for medical innovations. Collaborate with clinicians and health authorities to implement strategies that reduce barriers to patient access.
Manage a portfolio of Business Banking clients by providing expert health, safety, and environmental consultancy. Drive new business growth through networking and referrals while ensuring high-quality service delivery and client retention.
The role involves providing statistical support throughout the project lifecycle, from protocol development to the creation of Clinical Study Reports. Key duties include preparing Statistical Analysis Plans, coordinating biostatistics personnel, and ensuring the quality of project deliverables.
Deliver evidence-based CBT interventions to children and young people experiencing anxiety and depression. Perform clinical assessments and risk management while collaborating with a multidisciplinary team of psychologists and therapists.
Deliver high-quality systemic family therapy interventions to children, young people, and their families to improve relational dynamics. Conduct comprehensive assessments and work within a multidisciplinary team to support emotional wellbeing.
Regional Medical Advisor
Dr Reddy's Laboratories Limited
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Full Time
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3 Days Ago
Dr Reddy's Laboratories Limited
Act as the primary scientific face of the organization to engage thought leaders and physicians within a specific therapy area. Responsible for executing strategic medical affairs plans, generating medical evidence, and providing scientific expertise to support optimal patient outcomes.
Conduct intensive nutrition counseling and weight management education via various digital communication channels. Provide medication support and remote patient monitoring for cardiometabolic health under physician supervision.
Bilingual (Spanish) Telehealth Certified Diabetes Educator
Cecelia Health
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Full Time
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3 Days Ago
Cecelia Health
Provide diabetes education and support to patients via phone to improve health outcomes and adherence. Responsibilities include conducting motivational interviewing, presenting online webinars, and meeting program quality metrics.
Develop and maintain certification exam items, blueprints, and educational resources for healthcare credentials. Collaborate with subject matter experts and utilize AI tools to ensure exam quality and alignment with industry standards.
Coordinate RFP activities, including the development of proposals, pricing, and budgets for new and existing clinical research opportunities. Manage change orders and maintain Salesforce to support wider business development and market intelligence.
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Perform medical review of complex safety cases and ensure compliance with global drug safety regulations and reporting timelines. Act as a Subject Matter Expert to mentor junior physicians and support audits, inspections, and process improvements.
The representative is responsible for delivering professional presentations to doctors and healthcare organizations to increase prescriptions for Pfizer products. They must manage territory call plans, track competitive activities, and ensure product availability at the retail level.
Manage regional business goals, budgets, and market risk while maintaining professional partnerships with pharmacy customers. Execute product promotion strategies and ensure all activities comply with company financial and legal standards.
Experienced CRCs & CRAs | Relocate to Brisbane and Advance Your Clinical Research Career
Thermo Fisher Scientific
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Full Time
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4 Days Ago
Thermo Fisher Scientific
Perform and coordinate all aspects of clinical monitoring and site management, including source data verification and visit report preparation. Ensure studies are conducted in accordance with ICH-GCP and regulatory requirements while maintaining strong relationships with investigational sites.
Quality & Safety Improvement Consultant V, ICU Clinical - Remote, Per Diem
Kaiser Permanente
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Full Time
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4 Days Ago
Kaiser Permanente
Provides expert consultation on clinical quality, patient safety, and regulatory compliance to optimize patient outcomes and reduce practice variation. Develops data-driven quality improvement initiatives and monitors compliance with state and federal healthcare standards.
The specialist manages client requests regarding pharmacy contracts, rebates, and credits while serving as an on-site subject matter expert for ordering platforms. They are responsible for generating performance metrics and collaborating with internal stakeholders to drive customer satisfaction and growth.
Neuroscience Specialist, Health and Science Professional - Wellington, FL
Pfizer
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Full Time
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4 Days Ago
Pfizer
The Neuroscience Specialist is responsible for driving sales and developing relationships with customers in an assigned territory to promote breakthrough migraine therapies. This involves implementing strategic business plans and utilizing digital tools for both virtual and in-person provider engagement.
Oversee outreach to veterinary students and academic professionals to increase brand awareness and engagement with AVMA Insurance Services. Collaborate with internal teams to develop educational content and support the transition of students into professional practice.
The Medical Scribe is responsible for documenting patient encounters in real time and updating electronic health records with precision. They also assist with coding, billing documentation, and managing patient follow-ups and referrals.
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The Medical Scribe is responsible for documenting patient encounters, history, and treatment plans in real-time within electronic health records. They also manage patient follow-ups and ensure all medical documentation complies with HIPAA regulations.
The Medical Scribe is responsible for documenting patient encounters, history, and treatment plans in real-time within electronic health records. They also manage patient follow-ups and ensure all medical documentation is accurate and HIPAA compliant.
The role involves coordinating the setup and monitoring of clinical trials, ensuring accurate study status reports and documentation. It also requires maintaining strong relationships with investigators and ensuring patient safety through strict regulatory compliance.
The In-House CRA supports site management and monitoring activities to ensure clinical trials comply with protocols, SOPs, and regulatory requirements. Key tasks include maintaining essential documents in the Trial Master File and tracking trial progress via CTMS.
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