Start-up Specialist I

Job Location(s) TW
Job Number
Job Category
Clinical Operations
Position Type

Job Overview

Already working in the clinical trial industry and open to explore potential career opportunities? We are currently hiring Start-up Specialist for the right professionals to join our Clinical Operations team in Taiwan. By joining our Clinical Development Services business operations in Taiwan, you will be participated in variouus clinical studies with a professional team. If you are ready for an exciting and challenging opportunity, we would love to talk to you!



Preparation of submission package for IRB/ERC and support regulatory agencies submissions.

Collaborate with finance/budgeting representatives for payments (investigators, vendors, grants)

Document management: 1) Prepare documents and correspondence, 2) Collate, distribute, and archive clinical documents (i.e. TMF), 3) Updating trial manuals/documents (e.g., patient diaries, instructions).

Trial and site administration: 1)IMP (Study drug) management, 2) Safety reporting, 3)Specimen export management, 4) Warehouse management

About Covance:

Covance is one of the world's largest and most comprehensive drug development services companies, with more than 11,000 employees in 60 countries. We began operations Asia Pacific in 1988 and today have more than 1000 employees in 14 countries across the region. Through our discovery, nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.


Why Covance?

At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.

We welcome your application and believe this decision may be the most rewarding career move you will ever make!


  • University degree with life science preferred
  • Fluent in local language and English


  • Candidate with 1 year or more relevant RA/IRB submission experience in pharma or CRO in Clinical Research field
  • Thorough knowledge of ICH GCP and regulatory


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