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Salary
≈ $18k – $33k per year (Estimated)
Location
In office (Singapore)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 5, 2026. First seen by Alion on Oct 24, 2026. Parexel scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Parexel is a clinical research organisation headquartered in Durham, North Carolina that provides Phase I to IV clinical trial services, regulatory consulting, market access and safety services to biopharmaceutical companies. Founded in 1983 and owned by EQT and Goldman Sachs since 2021, it employs more than 21,000 people, with large teams in the US, Hyderabad, Bengaluru, London, Poland, Romania, Serbia and Bloemfontein. Its openings are mostly for regulatory affairs consultants and associates, clinical research associates, safety technology analysts, clinical trial managers, data and AI engineers, many of them home or office based.

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.

Key Accountabilities:

Role specific

  • Receiving and stocking of materials
  • Pick and pack and quality control of Clinical Trial Materials according to instruction
  • Perform quality control checks
  • Prepare for study documents
  • Dispatch materials
  • Assistance and execution in packaging and labeling including relabeling procedures
  • Assistance in Clinical Trial Materials destruction, recalls, reconciliation and returns
  • Execute regular cycle count and physical inventory
  • All tasks related warehouse management including production activities
  • Assistance and execution in Premise and Equipment general management
  • Report any issue affecting quality and/or deviation
  • Handle filing and archiving activities
  • Follow internal and external (ie. Client) work flows and processes
  • Strive to contribute to external and internal customer satisfaction
  • Complete trainings in time
  • Effectively and efficiently manage multiple tasks

Skills:

  • Team player with very good interpersonal skills
  • Local language proficiency (verbal and written)
  • Ability to effectively and efficiently manage multiple tasks
  • Proficient in Microsoft Office (Word, Excel and Power Point)
  • Good hand eye coordination

Knowledge and Experience:

  • Knowledge of GxP guidance, or willingness for education in GxP regulations
  • Basic understanding of the drug development and regulatory framework
  • Knowledge of warehouse management system and/or inventory system
  • Experience in a warehouse support (Packaging and labeling experience in pharmaceutical or biological industry is preferred)

Education:

  • High School or Vocational degree or 2-4 years relevant work experience.
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