Clinical Trial Assistant 2

Ivivamedical

Site activation activities
Regulatory document preparation
Clinical systems and databases
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.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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 document preparation
  • Clinical systems and databases
  • GCP/ICH guidelines knowledge
  • Local regulatory requirements

Nice-to-have

  • Effective communication skills
  • Ability to work independently
  • Negotiating and challenging skills
  • Understanding of drug development

Key Requirements

  • Bachelor's Degree in life sciences
  • 1-2 years clinical research experience
  • Fluent English (conversational)
  • Ability to manage multiple projects

Work Rights

Not specified

Tailored Resume

Cover Letter