_{04th April, 2025}

Avance Clinical is a Contract Research Organization which offers specialized services supporting drug development for the pharmaceutical and biotech industry
Job Overview

We are seeking Study Start-Up Specialist who also has experience in Investigations, Contracts/Payments to join our team. Ideal candidates will have minimum of 1-2 years of experience in Clinical Study Start-Up within the United States and at least 4 years of experience in the clinical research industry.


The SSU/ICP Specialist is responsible for executing site start up activities including review of initial regulatory documents, confidentiality agreements (CDAs) and clinical trial agreements (negotiating legal terms and site budgets) (CTAs) from the point of site activation to activation ready as well as processing site payments through to site close, in accordance with the protocol, company Standard Operating Procedures (SOPs), ICH GCP guidelines and other applicable regulatory requirements. They will report study progress to the Manager, Investigator Contracts and Payments.

Education Requirements

• Minimum bachelor’s level degree in life sciences, accounting, paralegal studies, pharmacy, nursing, or equivalent field (highly regarded), or
• appropriate industry experience.
• Must have previous experience in an equivalent role in a CRO is strongly preferred, Pharma company or investigator site, with a minimum of 1-2 years SSU experience in the United States and a minimum 4 years in the clinical research industry.
• Awareness of ICH GCP Guidelines and other applicable regulatory requirements (desirable).