Clinical Trials Assistant – Quality Assurance

RecruitGo

Muntinlupa

On-site

PHP 600,000 - 800,000

Full time

14 days+

Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Benefits offered by this job

Performance Bonus

13th Month Pay

HMO Health Insurance

Work from Home

Company Social Events

Company Equipment

Job summary

A leading Employer of Record company is seeking a Clinical Trials Assistant for a hybrid role in Muntinlupa. You will assist in clinical trial operations with an emphasis on data quality, compliance, and audit readiness. The ideal candidate should have a bachelor's degree in a relevant field, with 3-4 years of experience in clinical trials or data management. Strong organizational and detail-oriented skills are essential. The position offers a performance bonus, HMO health insurance, and work-from-home options.

Qualifications

3-4 years experience in clinical trials or healthcare data management.
Experience with international teams is an advantage.
Background in clinical data entry or quality assurance preferred.

Responsibilities

Assist in reviewing clinical trial protocols and related documentation.
Coordinate and track clinical trial schedules and timelines.
Prepare and ensure audit-ready clinical trial data for inspections.

Skills

Clinical data management

Attention to detail

Organizational skills

Communication skills

Education

Bachelor’s degree in medical or allied health-related field

Tools

CRIO

Medidata

EDC

CTMS

Job description

Clinical Trials Assistant – Quality Assurance

Hybrid - Muntinlupa 3-5 Yrs Exp Bachelor Full-time

Job Description

RecruitGo is a leading Employer of Record (EOR) company specializing in bridging top talent in emerging markets with global clients. This role supports clinical trial operations with a focus on data quality, compliance, and audit readiness.

Responsibilities

Assist in reviewing clinical trial protocols and related documentation
Coordinate and track clinical trial schedules, activities, and timelines
Maintain accurate, complete, and up-to-date patient and trial records
Prepare, verify, and ensure audit-ready clinical trial data for site visits and inspections
Perform data entry and ongoing data maintenance across clinical systems and third‑party platforms (e.g., CRIO, Medidata)
Support quality assurance processes to ensure compliance with regulatory requirements and internal standards
Collaborate with internal and external stakeholders to ensure smooth trial execution

Requirements

Bachelor’s degree in a medical or allied health‑related field (e.g., Nursing, Pharmacy, Medical Technology, Biology)
At least 3–4 years of relevant experience in clinical trials, healthcare data management, or similar roles
Experience working with international or cross‑functional teams is an advantage
Background in clinical data entry, data management, or quality assurance is preferred
Hands‑on experience with multiple healthcare or clinical systems (e.g., EDC, CTMS, or similar platforms)
Strong attention to detail, organization, and documentation skills

Benefits