Your Role
Key responsibilities as follows:
- Prepare and submit clinical trial documents, contracts, and materials.
- Communicate and collaborate with various departments to support clinical trial projects.
- Translate and verify clinical-related materials.
- Maintain communication and coordination with suppliers.
- Manage the clinical trial system.
- Upload supplier invoices and certification documents.
- Coordinate the signature and stamping of clinical documents.
- Visit local clinical institutions for management purposes if necessary.
About You
The ideal candidate will possess:
- Proficiency in office software and strong English reading, writing, and communication skills.
- Attention to detail, responsibility, and the ability to multitask and work in a team.
- Strong initiative and interest in clinical practice.
- Availability for at least 3-4 days a week and readiness for interviews soon.
- Preference for candidates with over 4 months of experience, a medical-related background, and internship experience.
Benefits
Enjoy a valuable internship experience with a global leader in consumer health, a supportive supervisor, and a harmonious work environment. Benefit from an excellent office location, unlimited coffee and tea, and afternoon tea.
Training & Development
Gain hands-on guidance and deep involvement in complete project processes, enhancing your professional development.
Career Progression
Opportunities for growth within the company, joining the core elite team, and advancing in the consumer health industry.
How to Apply
Submit your application by following the instructions provided by the Haleon recruitment team. If accommodations are needed, inform your recruiter with specific requests.
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