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The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, oversee project financials, and ensure compliance with ICH GCP and regulatory requirements.
Lead or support clinical data management study activities, CRO oversight, and delivery timelines while coordinating with client stakeholders and cross-functional teams to ensure high-quality, timely data deliverables. Manage vendor budgets and risks, maintain operational processes and inspection-ready records, and contribute to regulatory readiness, governance, and continuous improvement.
The Cybersecurity Technical Lead will act as the primary technical point of contact for clients, overseeing security posture, governance, and the execution of security controls. They are responsible for coordinating multidisciplinary teams, managing vulnerability remediation, and ensuring alignment with NIST frameworks.
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The psychiatrist will conduct comprehensive psychiatric assessments and diagnostic evaluations for patients in emergency and acute care settings. They are responsible for creating individualized treatment plans, prescribing medications, and coordinating care with a multidisciplinary team.
The Medical Director provides medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. They also manage safety variables, perform medical reviews of adverse events, and provide medical consultation to project teams and clients.
The Clinical Care Coordinator serves as a liaison between patients, providers, and insurance companies to ensure timely and well-coordinated care. Responsibilities include managing patient intake, documenting clinical information in EHR systems, and facilitating referrals and insurance authorizations.
The Clinical Trial Coordinator provides administrative and technical support to project teams while ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate communication between internal teams and clinical sites.
The specialist will manage appointment scheduling and CRM workflows using Vagaro while handling high-volume inbound patient inquiries. They are also responsible for providing patient navigation assistance and answering pre- and post-procedure questions to support the clinical team.
The coordinator acts as a liaison between patients, families, and healthcare staff to ensure effective communication and high-quality care delivery. Responsibilities include managing schedules, documenting interactions in HHA Exchange, and resolving case-related issues promptly.
The Executive Assistant will manage medical records, coordinate record requests, and provide administrative support to case managers within a personal injury law firm. Responsibilities include reviewing medical documentation for accuracy, identifying missing records, and maintaining organized case files using specialized software.
The Medical Scribe is responsible for accurately documenting patient encounters and updating clinical information within the EMR/EHR system. They also assist healthcare providers with chart preparation and ensure all documentation meets clinical and privacy standards.
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.
The role involves managing inbound patient calls, scheduling appointments, and handling patient intake and insurance verification. Additionally, the receptionist will process medication prior authorizations and maintain accurate patient records within a pain management clinic.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, develop study tools, and ensure compliance with ICH GCP and regulatory standards throughout the trial lifecycle.
The psychiatrist will conduct comprehensive psychiatric assessments and diagnostic evaluations for patients in emergency and acute care settings. They are responsible for creating individualized treatment plans, prescribing medications, and collaborating with a multidisciplinary team to provide coordinated care.
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The Senior Clinical Data Manager oversees the entire data management process from study set-up to close-out, ensuring data integrity and regulatory compliance. They act as the primary contact for clients and suppliers while mentoring junior staff and coordinating cross-functional study activities.
The role involves managing frontline patient communication, including scheduling appointments, verifying insurance, and handling prior authorizations. The assistant will also provide administrative support to ensure smooth clinic operations for a US-based skin clinic.
Manage pre-admission and prior authorizations with insurance providers while conducting concurrent reviews and clinical chart audits. Coordinate with clinical teams and support peer-to-peer reviews to ensure accurate authorization records and prevent coverage gaps.
Manage a high-volume caseload of approximately 100 clients, guiding them through the end-of-life service lifecycle from contract to final resolution. Coordinate with internal teams and vendors to ensure seamless execution of transportation, documentation, and cremation scheduling.
The Clinical System Lead directs project teams in the initiation, planning, maintenance, and closing of clinical trial systems. They also support business development, manage vendor interactions, and ensure quality control of technical documentation.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring compliance with regulatory requirements and managing safety-related event reporting.
The Clinical Trial Manager is responsible for leading clinical study site management activities and ensuring compliance with study protocols and SOPs across a geographic region. They will oversee site monitoring, manage project deliverables, and provide leadership to clinical staff to ensure high-quality data and timely study execution.
The Trial Delivery Specialist will manage end-to-end clinical study operations, including vendor oversight, eTMF maintenance, and project planning. They will partner with global study leaders to ensure inspection readiness, budget compliance, and the successful delivery of clinical trials.
Manage a caseload of Workers' Compensation cases from initial intake through to settlement. Coordinate with clients, medical providers, and attorneys to ensure accurate documentation and timely case progression.
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The Paid Media Supervisor will lead end-to-end strategy, execution, and performance management for multi-channel paid media accounts. They are responsible for mentoring a team of media managers, driving account growth, and acting as the primary point of contact for clients.
The role involves managing personal injury cases by coordinating between clients, medical providers, and legal staff while monitoring case progress. Responsibilities also include conducting client intake, maintaining accurate records, and ensuring all case deadlines are met.
The receptionist will manage patient communications, schedule appointments, and verify insurance information in both English and Spanish. They are also responsible for maintaining medical records, handling referrals, and ensuring HIPAA compliance within a behavioral health practice.
The consultant will be responsible for configuring SAP HCM Time Management and performing troubleshooting to resolve configuration errors. They will also manage various shift types and work schedules to meet client needs.
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