Parexel

Intern Clinical Data Analyst (CDA)

Parexel · Petaling Jaya, Selangor, Malaysia

Pharmaceutical Manufacturing · 10,001+ employees

13 h ago
Junior (0-2 yrs) Internship Malaysia
Log in to apply, save this posting, or score it against your profile with AI.

About the role

The intern will support clinical data management processes, including data cleaning, query management, and data review. They will also participate in database setup, User Acceptance Testing (UAT), and study start-up activities.

What they look for

Clinical Data Management Data Cleaning Query Management Data Review User Acceptance Testing (UAT) Database Setup ICH-GCP Compliance Quality Control Project Coordination Analytical Skills Problem-solving

Requirements

Applicants must be final-year undergraduate students majoring in Life Sciences, Pharmacy, Biotechnology, or related disciplines. Candidates must be available to work full-time for a 4 to 6 month internship starting September 2026.

Full description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

This is 4 to 6 months internship program starts from September 2026.

Location: Petaling Jaya, Parexel Malaysia Office

What You'll Gain

  • Hands-on exposure to clinical data management processes across the clinical trial lifecycle
  • Experience supporting data cleaning, query management, and data review activities
  • Opportunities to participate in database setup, User Acceptance Testing (UAT), and study start-up activities
  • Insight into clinical research quality standards, including ICH-GCP compliance and quality control processes
  • Experience working with clinical trial data and documentation in a global CRO environment
  • Development of analytical, problem-solving, attention-to-detail, and project coordination skills
  • Collaboration with experienced Clinical Data Management professionals and cross-functional teams
  • Practical industry experience that will help prepare you for a career in clinical research, data management, and life sciences

Eligibility

  • Final-year students who are required to complete an internship / industrial training as part of their degree program
  • Undergraduate students majoring in Life Sciences, Biomedical Sciences, Biotechnology, Pharmacy, Biochemistry, Microbiology, or related disciplines
  • Available to work full-time throughout the internship period