北京招聘

Overall, to be accountable for efficiently managing drug Import and export process and supporting study manager(s) with the execution of drug supply, and support overall compliance with GCPs and ICON SOPs, including:

1. To manage drug Import and export process;

2. To have thorough understanding of clinical trials supply chain;

3. To assist project manager with study drug supply, labeling and transportation ;

4. To contribute to IMP related SOPs and guidelines and provide training to operation team;

5. To co-ordination of clinical drug related contract and payments;

6. To coordinate communication with Customs Clearance, internal stakeholders and vendors, if applicable.

Qualification:

Education(minimum/desirable): Bachelor degree Preferred;

Languages: Fluent in English written and spoken;

Requirements:

1. Ideally 5 years work experience with 3+year experience in IMP or supply chain

2. Creativity and flexibility

3. Able to work in a matrix organization

4. Team player

5. Ability to work under pressure

6. Demonstrates collaboration skills

7. Effectively prioritizes workload

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.