Clinical Research Associate I/II — Field Trials Lead

Parexel; Hong Kong; Hybrid; HKD 420,000 - 560,000; Full time

Job summary

Parexel in Hong Kong is seeking a CRA I or II for our Global FSP Team. You will conduct site management, monitoring visits, and ensure protocol adherence across multiple sites with focus on data quality and patient safety.

The role requires occasional travel to client offices 1-2 days per week and collaboration with cross-functional teams to drive study timelines and regulatory compliance. Strong communication and problem-solving skills are essential.

Qualifications

• Site Management experience or equivalent in clinical research.
• Excellent communication and collaboration with cross-functional teams.
• Knowledge of ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Act as Parexel’s direct contact with assigned sites and ensure study protocol adherence.
• Build relationships with investigators and site staff.
• Support site access to study systems and ensure training compliance.
• Evaluate staffing and implement corrective actions as needed.
• Address site-related issues and training gaps.
• Follow up on site questions and data queries.
• Participate in audits and regulatory inspections as required.
• Manage site documentation and TMF submission.

Skills

Problem solving

Initiative

Presentation skills

Client focus

Professionalism

Flexibility

Time management

Teamwork in matrix

CTMS proficiency

Communication

Urgency

Cross-cultural

Quality focus

Virtual collaboration

Consulting

Attention to detail

Travel readiness

Driver's license

Education

Biological science or pharmacy degree

Tools

CTMS

EDMS

MS Office

Job description

Parexel in Hong Kong is seeking a CRA I or II for our Global FSP Team. You will conduct site management, monitoring visits, and ensure protocol adherence across multiple sites with focus on data quality and patient safety.

The role requires occasional travel to client offices 1-2 days per week and collaboration with cross-functional teams to drive study timelines and regulatory compliance. Strong communication and problem-solving skills are essential.