Jobs at Angel City VA

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 Remote Nurse provides virtual patient support, conducts health assessments, collaborates with physicians, and documents care via EHR.

The Clinical Trial Nurse will support clinical trial activities, conduct patient recruitment and enrollment, provide patient education, and collaborate with teams to ensure adherence to protocols.

The Business Development Specialist will engage clients, implement sales strategies, and collaborate on onboarding to expand the clinical trials network.

As a Remote Business Development Specialist, you will engage clients, develop sales plans, collaborate with teams, and stay informed on clinical trial opportunities.

The role involves managing clinical trials, ensuring compliance with GCP guidelines and EDC standards, and maintaining documentation.

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

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 Bookkeeper will manage financial records, process transactions, prepare reports, assist in budgeting, and ensure compliance with tax regulations.