AstraZeneca

Biopharmaceutical

R&DIntern

Hong Kong, China FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“R&D Intern at AstraZeneca. Skills: Document management, Systems maintenance, Quality checks. Review study documents. Upload and file documents”

What You'll Achieve.

Ensure inspection-ready documentation; Efficient site start-up

Industry & Context.

Biopharmaceutical
Problems you'll solve

Resolve gaps or discrepancies

What They're Looking For.

Must Have

Currently pursuing a bachelor’s degree (or master’s) in life sciences, pharmacy, public health, health administration, or a related field., Proven accuracy in reviewing documents and handling structured information., Ability to prioritize tasks and meet deadlines across multiple workstreams., Clear written and verbal communication in both English and collaborative mindset.

What You'll Do.

Review study documents

Upload and file documents

Prepare investigator site folders

Support study systems maintenance

Work closely with R&D team

How You'll Work.

Team & Collaboration

Work closely with study team members; Coordinate updates with study team; Work closely with R&D team; Collaborate with cross-functional teams

Communication Scope

Clear written communication; Clear verbal communication; English communication

Process & Methodology

Prioritize tasks, Meet deadlines

Full Job Description

_Do you have expertise in, and passion for providing medical and scientific support? Would you like to apply your expertise to impact the lives of patients in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!_ **ABOUT ASTRAZENECA** _AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. We are on a journey to bring life-saving medicines to patients. Our role in contributing to decreasing mortality rates globally is clear – shaping the future by spotting a scientifically-led commercial opportunity and acting now to operationalise and scale it._ **What you’ll do** The R&D Intern will support clinical study operations with a focus on document management and systems maintenance. Working with the study team, you will perform quality checks in the electronic filing system, prepare investigator site folders, and help maintain core study systems to ensure inspection‑ready documentation and efficient site start‑up. **Key Responsibilities** * Review and verify study documents in the electronic filing system for accuracy, completeness, correct filing locations, and metadata. * Upload, file, and reconcile documents against study file plans; flag and resolve gaps or discrepancies with study team members. * Prepare and QC investigator site file folders and associated materials for site activation and maintenance; coordinate updates as documents are amended. * Support routine maintenance of study systems, including data entry, status updates, user access requests, and audit trail checks per guidance. * Follow applicable SOPs, work instructions, and GCP/data integrity standards; help keep documentation inspection‑ready. * Work closely with R&D team, and cross‑functional partner

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