Site Activation Specialist (ssu/rsu)

IQVIA UK

Taipei, Taiwan
Site activation activities
Regulatory compliance
Project timelines
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines

Job Summary

  • Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
  • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
  • Provide local expertise to SAMs and project team during initial and on-going project timeline planning.

Matching Summary

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.

Skills & Requirements

Must-have

  • Site Activation activities
  • Regulatory compliance
  • Project timelines
  • Clinical systems and procedures
  • GCP/ICH guidelines

Nice-to-have

  • Effective communication
  • Organizational skills
  • Interpersonal skills
  • Ability to work independently
  • Manage multiple projects

Key Requirements

  • 3 years clinical research experience
  • 1 year leadership capacity experience
  • Bachelor’s Degree in life sciences or related field
  • Knowledge of applicable regulatory requirements
  • Understanding of regulated clinical trial environment

Work Rights

Not specified

Tailored Resume

Cover Letter