Site Activation Specialist

2 weeks ago


Reading, Reading, United Kingdom IQVIA Full time

Job Overview


Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics.

Also serves as the primary point of contact for investigative sites.

**Duties

  • Perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites
  • Prepare site documents, reviewing for completeness and accuracy.
  • Inform team members of completion of regulatory contractual. and other documents for individual sites.
  • Distribute completed documents to sites and internal project team members.
  • Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
  • Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications

  • Bachelor's Degree Life sciences or a related field
years' clinical research or other relevant experience

  • Or 3 years' experience in a healthcare environment or equivalent combination of education, training and experience.


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