Remote Clinical Trial Support Specialist
A
Angel City VAClinical Research
Remote (Philippines, Latin America, Ireland, Portugal, Spain, and Italy).Full-TimeMiddle
Salary not disclosed
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Job Details
- Languages
- Excellent English written and verbal communication skills; multilingual skills are highly desirable.
- Experience
- 2-3 years
- Required Skills
- GCPEHRHIPAAData entry
Requirements
- 2-3 years of experience supporting clinical trials, research sites, CROs, or healthcare organizations.
- Medical or biopharmaceutical background, education, or equivalent experience.
- Completed and current GCP (Good Clinical Practice) training.
- Completed and current HIPAA training.
- Familiarity with GCP principles and ICH E6(R3) guidelines.
- Experience with CTMS, EDC, EMR/EHR, or eRegulatory software.
- Strong organizational and documentation skills.
- Excellent English written and verbal communication skills.
- Ability to work independently and reliably in a remote environment.
- Submission of 3 references from previous clinical trial positions.
Responsibilities
- Walk participants through study procedures and visit expectations.
- Book participant visits, send reminders, and reduce no-shows.
- Conduct preliminary eligibility screening against study criteria.
- Update and maintain electronic medical records (EHR/EMR).
- Enter and maintain data in CTMS, EDC, and other research systems.
- Maintain e-regulatory binders and manage document version control.
- Support source-data verification (SDV) and audit readiness.
- Monitor investigational product storage temperatures remotely.
- Assist with study startup, maintenance, and closeout activities.
- Support logging of adverse events (AEs) and serious adverse events (SAEs).
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