Jobs at Angel City VA

Paid remote part-time internship combining light accounting, financial record organization, data entry, and executive administrative support. The intern will maintain accurate records, assist with reports and daily operations, communicate in Hebrew and English, and support additional projects while gaining experience with a U.S.-based healthcare corporation.

Provides remote administrative and clinical research support, including patient visit scheduling, IRB submissions, informed consent documentation, study start-up activities, contract and budget coordination, vendor communication, and study file maintenance. The role supports the Site Manager, tracks outstanding tasks, assists with the transition to an eSource system, and helps ensure accurate, timely completion of research-site activities and a positive patient experience.

Provides remote administrative and research support for clinical study start-ups, contracts, budgets, patient visit coordination, IRB submissions, informed consent documentation, vendor coordination, and study records. The role supports the Site Manager, tracks outstanding tasks, helps transition the site to an eSource system, and ensures accurate, timely completion of clinical research activities while promoting a positive patient experience.

Provides remote administrative and clinical research support, including patient visit scheduling, study start-up activities, IRB submissions, informed consent documentation, vendor and facility coordination, contract and budget tracking, and study documentation management. Follows up on outstanding tasks, supports the transition to an eSource system, and helps improve research site workflows and patient experience.

Provides remote administrative and research support for clinical study start-ups, patient visit coordination, IRB and informed consent documentation, vendor and facility coordination, budget and contract tracking, and study file maintenance. The role supports eSource implementation, follows up on outstanding tasks, and helps ensure accurate, timely completion of site activities and a positive patient experience.

Provides remote administrative and research support for clinical study sites, including patient visit scheduling, IRB submissions, informed consent documentation, study start-up, vendor and facility coordination, contract and budget tracking, and study file maintenance. Follows up on outstanding tasks, supports eSource implementation, and helps ensure accurate, timely completion of clinical research activities while maintaining a positive patient experience.

Provides remote support across the clinical trial lifecycle, including patient education, recruitment, scheduling, data entry, source documentation, regulatory submissions, quality assurance, compliance, sponsor/CRO coordination, study startup and closeout, safety reporting, finance, and decentralized trial workflows. Candidates may specialize in one or more functional areas and must maintain accurate, audit-ready records while communicating effectively with participants and study stakeholders.

Provides remote support across the clinical trial lifecycle, including patient education and recruitment, visit scheduling, data entry, source management, regulatory documentation, quality assurance, safety reporting, study startup and closeout, sponsor/CRO coordination, finance administration, and decentralized trial operations.

Provides remote support across clinical trial operations, including patient education, recruitment, scheduling, data entry, source documentation, regulatory submissions, quality assurance, safety reporting, study startup, sponsor/CRO coordination, and decentralized trial workflows. Maintains audit-ready records, supports participant compliance, coordinates reimbursements, and assists with EHR/EMR, clinical research systems, and investigational product documentation.

Provides remote support across clinical trial operations, including patient education, recruitment, scheduling, data entry, source documentation, regulatory support, quality assurance, sponsor and CRO coordination, reimbursement processing, study startup and closeout, safety reporting, and decentralized trial workflows. Specialists may focus on one or more functional areas and must maintain accurate, compliant, audit-ready records while communicating effectively with participants and study stakeholders.

Supports clinical trial operations remotely across patient engagement, visit scheduling, recruitment, data entry, regulatory documentation, quality assurance, safety reporting, study startup, sponsor/CRO relations, and decentralized trial coordination. Maintains accurate, compliant, audit-ready records in clinical research systems, assists with participant communication and retention, tracks study milestones and credentials, and supports financial, reimbursement, monitoring, and investigational product documentation.

Supports clinical trial operations remotely across patient engagement, scheduling, recruitment, data entry, source documentation, regulatory compliance, quality assurance, sponsor and CRO coordination, financial administration, safety reporting, and decentralized trial workflows. Maintains accurate, audit-ready records and supports study startup, monitoring, closeout, participant compliance, and telehealth activities. Candidates may specialize in one or more functional areas and must demonstrate strong English communication, organization, and independent remote-working skills.

Provides remote support across clinical trial operations, including participant education and recruitment, visit scheduling, data and source management, regulatory documentation, quality assurance, safety reporting, study startup, sponsor/CRO coordination, financial administration, and decentralized trial workflows. Maintains accurate, compliant, audit-ready records while supporting research sites and study teams. Roles require clinical research experience, GCP and HIPAA training, strong documentation skills, and familiarity with clinical trial systems.

Provides remote support across clinical trial operations, including participant education, scheduling, recruitment, data entry, source documentation, regulatory maintenance, quality assurance, safety reporting, study startup, sponsor/CRO coordination, reimbursements, and decentralized trial workflows. The role may also support EHR management, financial administration, credentialing, investigational product compliance, monitoring readiness, and bilingual participant communication.

Provides remote support across clinical trial operations, including patient engagement, visit scheduling, recruitment, pre-screening, data entry, regulatory documentation, quality assurance, sponsor and CRO coordination, reimbursement, study startup, safety reporting, telehealth visits, and investigational product monitoring. Maintains accurate, compliant, audit-ready records and supports research sites throughout the trial lifecycle.

Provides remote clinical trial support across patient engagement, visit scheduling, recruitment, data entry, regulatory documentation, quality assurance, sponsor/CRO coordination, financial administration, study startup, safety reporting, and decentralized trial workflows. Maintains accurate, compliant, audit-ready records and supports research sites throughout the clinical trial lifecycle. Candidates may specialize in one or more functional areas and must communicate clearly, work independently, and maintain current clinical research training.

Provides remote support across clinical trial operations, including patient education and recruitment, visit scheduling, data and source management, regulatory documentation, quality assurance, safety reporting, study startup and closeout, sponsor/CRO coordination, reimbursements, and decentralized trial workflows. Candidates should have clinical research or healthcare-related experience, strong documentation and communication skills, current GCP and HIPAA training, and familiarity with clinical research systems.

Supports clinical trial operations remotely across patient engagement, visit coordination, recruitment, data entry, regulatory documentation, quality assurance, sponsor and CRO relations, study startup, safety reporting, telehealth, and financial administration. Maintains accurate, compliant, audit-ready records in clinical research systems and helps coordinate participants, sites, investigators, sponsors, and CROs throughout the study lifecycle.

The Virtual Administrative Assistant will manage schedules, facilitate communication, perform data entry, organize files, and provide customer service support while ensuring efficiency in operations remotely.

The Remote Nurse provides patient support via virtual channels, conducts health assessments, educates on treatment plans, and collaborates with healthcare providers.