Site Activation Specialist, Sponsor Dedicated (contract)

IQVIA UK

Not specified (assumed hybrid or onsite based on industry norms)
Site activation and feasibility execution
Regulatory document review and negotiation
Contract management and execution tracking
IQVIA UK is seeking a Site Activation Specialist for a 6-month contract to manage site activation activities in compliance with regulations and project requirements. The ideal candidate will have a background in life sciences, experience in regulatory submissions, and strong communication skills

Job Summary

  • This role serves as the Single Point of Contact for site activation, feasibility, and maintenance activities in assigned studies.
  • The specialist is responsible for preparing, reviewing, and distributing essential regulatory documents such as Informed Consent Forms and Investigator Packs.
  • Candidates must possess at least one year of Start Up experience and specific IRB submission background to support global clinical research initiatives.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Site Activation Specialist for a 6-month contract to manage site activation activities in compliance with regulations and project requirements. The ideal candidate will have a background in life sciences, experience in regulatory submissions, and strong communication skills.

Skills & Requirements

Must-have

  • Site activation and feasibility execution
  • Regulatory document review and negotiation
  • Contract management and execution tracking
  • IRB submission experience required
  • Start up experience over one year

Nice-to-have

  • Strong English communication skills
  • Ability to work under moderate supervision
  • Experience with internal system updates
  • Collaboration with project management teams

Key Requirements

  • Bachelor's Degree in Life Sciences or related field
  • Mandatory IRB submission experience
  • Minimum one year of Start Up experience
  • Good English communication skills

Work Rights

Not specified

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