Remote Clinical Trial Operations Specialist

Visa Hunt

Philippines

Remote

PHP 1,505,000 - 3,009,000

Full time

14 days+
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Job summary

Angel City VA is actively building a global pipeline of remote clinical trial professionals. This role supports independent research sites, sponsors, and CROs in multiple therapeutic areas, leveraging 2–3 years of clinical research experience and a background in biopharma.

You will handle study operations, regulatory, data management, and patient interactions from a remote setting. The ideal candidate is detail-oriented, communicates clearly in English, and can work independently in a

Qualifications

  • Minimum 2–3 years in clinical research or related field.
  • Medical/biopharmaceutical background.
  • Completed and current GCP and HIPAA training.
  • Strong knowledge of GCP principles (ICH E6).
  • Experience with CTMS, EDC, EMR/EHR or similar platforms.
  • Excellent organizational and documentation skills.
  • Fluent English; multilingual abilities are a plus.

Responsibilities

  • Support independent clinical research sites, sponsors, CROs, and healthcare organizations in trial operations.
  • Engage in patient education, regulatory support, data management, and site coordination.
  • Maintain CTMS/EDC/EMR data accuracy and audit-ready documentation.
  • Assist with budgeting, contracting, and sponsor relations as needed.
  • Coordinate telehealth visits and remote trial activities.
  • Ensure compliance with privacy and regulatory requirements.

Skills

Clinical trials
Medical background
GCP training
HIPAA training
CTMS knowledge
EDC knowledge
EMR/EHR experience
Documentation skills
English fluency
Remote work
Multilingual

Education

Life sciences degree
Nursing/Pharmacy background

Tools

CTMS
EDC
EMR/EHR
eRegulatory tools

Job description

Angel City VA is actively building a global pipeline of remote clinical trial professionals. This role supports independent research sites, sponsors, and CROs in multiple therapeutic areas, leveraging 2–3 years of clinical research experience and a background in biopharma.

You will handle study operations, regulatory, data management, and patient interactions from a remote setting. The ideal candidate is detail-oriented, communicates clearly in English, and can work independently in a

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