Clinical Research Associate (Unblinded)
covance
Taipei City, Taiwan
12小时前

Job Overview :

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.

Performs clinical study site management / monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.

Gains an in-depth understanding of the study protocol and related procedures.

Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.

Participates & provides inputs on site selection and validation activities.

Education / Qualifications :

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

    more than 1 year site management experience

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