Site Activation Specialist

IQVIA UK

Bachelor's degree in life sciences
3 years clinical research experience
Knowledge of gcp/ich guidelines
The role serves as the Single Point of Contact for assigned studies, ensuring adherence to SOPs and project timelines

Job Summary

  • The role serves as the Single Point of Contact for assigned studies, ensuring adherence to SOPs and project timelines.
  • Responsibilities include preparing regulatory documents, negotiating site contracts, and managing internal systems and databases.
  • Candidates must possess in-depth knowledge of clinical systems, corporate standards, and applicable regulatory guidelines.

Matching Summary

The role serves as the Single Point of Contact for assigned studies, ensuring adherence to SOPs and project timelines.

Skills & Requirements

Must-have

  • Bachelor's Degree in life sciences
  • 3 years clinical research experience
  • Knowledge of GCP/ICH guidelines
  • Site contract and budget negotiation
  • Regulatory document preparation

Nice-to-have

  • Mentoring less experienced staff
  • Feasibility and site identification activities
  • Strong communication and negotiation skills
  • Experience with bid defenses and proposals
  • Ability to work independently

Key Requirements

  • Bachelor's Degree in life sciences or related field
  • Minimum 3 years of clinical research experience
  • Knowledge of local regulatory requirements and GCP/ICH

Work Rights

Not specified

Tailored Resume

Cover Letter