Senior Site Activation Specialist

Ivivamedical

Not specified
Site activation activities
Regulatory compliance
Project timelines
Ivivamedical is seeking a Senior Site Activation Specialist responsible for overseeing Site Activation activities in compliance with regulations and project requirements. The ideal candidate will have a background in clinical research, including experience in leadership roles

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.
  • Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.

Matching Summary

Match Score: 75

Ivivamedical is seeking a Senior Site Activation Specialist responsible for overseeing Site Activation activities in compliance with regulations and project requirements. The ideal candidate will have a background in clinical research, including experience in leadership roles.

Skills & Requirements

Must-have

  • Site Activation activities
  • regulatory compliance
  • project timelines
  • document quality control
  • investigative sites SPOC

Nice-to-have

  • recommendations for enhancements
  • local expertise
  • proactive problem solving

Key Requirements

  • Bachelor's Degree Life science or related field
  • 3 years clinical research experience
  • 1 year leadership capacity experience

Work Rights

Not specified

Tailored Resume

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