Remote Clinical Trial Support Specialist (Multiple Openings)
Remote · Philippines
Job Summary
Remote Clinical Trial Support Specialist role involves supporting independent clinical research sites, sponsors, CROs, and healthcare organizations across diverse trial operations functions. Key responsibilities include patient education and engagement, visit scheduling and coordination, recruitment and pre-screening, lead generation, EHR/EMR management, data entry and source management, regulatory support, quality assurance, IP compliance, contract and budget support, sponsor/CRO relations, reimbursements and stipends, bookkeeping and finance support, bilingual participant support, credentialing and credentialing tracking, administrative support, and telehealth/decentralized trial coordination. The role emphasizes remote, multi-area clinical trial operations with opportunities to specialize in one or more functional areas and requires familiarity with clinical research software platforms, regulatory requirements, and strong communication skills. Candidates should indicate which areas best match their experience, provide references, and are encouraged to share a short video introduction, software/tools used, languages, availability, and salary expectations.
Required Qualifications
- 2-3 years of experience in clinical trials, research sites, CROs, sponsors, or healthcare organizations
- Medical or biopharmaceutical background or equivalent experience
- Completed and current GCP and HIPAA training
- Familiarity with GCP (ICH E6) principles and regulatory guidelines
- Experience with CTMS, EDC, EMR/EHR, eRegulatory or other clinical research software
- Strong organizational and documentation skills
- Excellent English written and verbal communication
- Ability to work independently and reliably in a remote environment
- Multilingual skills desirable
- Willingness to specify functional areas of experience and provide references
Desired Qualifications
- 2-3 years of experience in clinical research or healthcare operations
- Medical or biopharmaceutical background or equivalent experience
- Completed and current GCP training
- HIPAA training
- Experience with CTMS, EDC, EMR/EHR, eRegulatory or other clinical research software
- Strong organizational and documentation skills
- Excellent English written and verbal communication
- Ability to work independently in a remote environment
- Multilingual skills is highly desirable
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.