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Description:* Review, administratively finalize (headers/footers/file name consistency) watermark and protect contracts and amendments. •* Print, asse
JOB SUMMARY Administers and negotiates site contracts that support projects within Clinical Operations on a global scale, with moderate oversight f...
This position plays as first point of contact a vital role in representing PAREXEL. Correct and friendly receipt of all visitors and guests, managing
Our client is a leading global healthcare communications and consulting business and are currently looking for an experienced medical writer.
The Opportunity 業務内容： ISO 13485/CEマーキング/PMD. Act審査における審査業務雇用形態： ①正社員 （他の認証機関での審査員としての活動内容による。） ②有期雇用契約社員 （認証機関での審査員未経験の方は有期雇用契約社員からのスタート。BSIで活動できる審査
Responsibilites: •* Partners with the LTM and Site Manager to ensure overall site management and adherence to internal SOPs, policies and local regula
IQVIA Biotech is the global, enterprise-wide solution that provides flexible, tailored, integrated clinical and commercial solutions to small biote...
Job responsibilities: •Management Clinical Trails according to the protocol and ICH GCP, standard operation procedures and monitoring plan. •Knowledge