Clinical Research Associate II - Site & Data Quality Lead

Parexel; Petaling Jaya; Sur place; MYR 120 000 - 180 000; Plein temps

Résumé du poste

Parexel seeks a Site Management professional to act as the primary liaison with clinical sites, ensuring protocol adherence and data integrity across studies in Malaysia. You will drive site training, recruitment strategy, and regulatory compliance while coordinating with internal teams to maintain TMF quality and timely study delivery.

The role requires extensive travel, strong problem-solving, and the ability to work in a matrix environment, with a focus on quality and patient safety.

Qualifications

• Experience in site management or clinical research is required.
• Educated to degree level in a health-related discipline or equivalent experience.

Responsabilités

• Act as Parexel’s site contact and ensure protocol adherence.
• Maintain CTMS/EDMS data and TMF quality across sites.
• Ensure audit readiness and regulatory compliance.
• Coordinate site training and engagement to support study timelines.
• Manage site recruitment and data quality with effective follow-up.

Connaissances

Problem solving

Independent work

Presentation skills

Client focus

Interpersonal communication

Teamwork

Time management

Travel flexibility

Driver's license

Matrix work environment

Formation

Bachelor's degree in biological science, pharmacy or health-related field

Outils

CTMS

EDMS

MS Office (Excel, Word)

Description du poste

Parexel seeks a Site Management professional to act as the primary liaison with clinical sites, ensuring protocol adherence and data integrity across studies in Malaysia. You will drive site training, recruitment strategy, and regulatory compliance while coordinating with internal teams to maintain TMF quality and timely study delivery.

The role requires extensive travel, strong problem-solving, and the ability to work in a matrix environment, with a focus on quality and patient safety.