Role:
We are seeking a dynamic and dedicated Clinical Research Associate (CRA) to join our clinical research team. In this pivotal role, you will be at the forefront of ensuring clinical trials are conducted in accordance with the study protocol, Standard Operating Procedures (SOPs), and applicable regulatory requirements (GCP). You will be responsible for monitoring study progress at various investigational sites, ensuring data quality and integrity, and acting as the primary liaison between the sponsor and the investigator.

Key Responsibilities:

  • Conduct monitoring visits (pre-study, initiation, monitoring, and close-out) to clinical trial sites (hospitals/clinics).
  • Verify the accuracy and completeness of Case Report Form (CRF) data against source medical records.
  • Ensure study compliance with the protocol, SOPs, Good Clinical Practice (GCP), and all applicable regulations.
  • Train and coordinate with site staff (Investigators, Study Coordinators).
  • Manage essential study documents related to the site (e.g., Informed Consent Forms, Investigator CVs, etc.).
  • Report study progress, monitoring findings, and critical issues to the relevant Project Manager.
  • Verify the accountability and storage conditions of investigational products/supplies at the site.

Qualifications We Are Looking For:

1. Education:

  • Bachelor's Degree (S1) in an Exact Science field (Pharmacy, Biology, Microbiology, Chemistry, Public Health, Medical Science, or other relevant life sciences).


2. Experience:

  • Preferably 1-2 years of experience as a CRA or Clinical Research team
  • Fresh graduates with a minimum GPA of 3.00 from exact science backgrounds who are highly motivated and willing to learn are strongly encouraged to apply.

3. Skills & Competencies:

  • Strong analytical skills and a keen eye for detail.
  • Excellent communication and interpersonal skills.
  • Ability to work both independently and as part of a team.
  • Strong time management and organizational skills.
  • Proficient in using Microsoft Office Suite.
  • Willingness to travel extensively to various study sites.

What We Offer:

  • Competitive salary and benefits package.
  • Continuous career development and training opportunities in clinical research.
  • A dynamic, collaborative, and international-standard work environment.
  • The opportunity to contribute directly to the development of new, life-saving drugs and therapies.


The application deadline is October 31st, 2025

We look forward to receiving your application!

Clinical Research Associate (CRA)

Brickhouse Ruko Exclusive Cisalak


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