Senior Site Activation Coordinator - IQVIA Biotech

IQVIA; United States; Remote; USD 85,000 - 120,000; Full time

Benefits offered by this job

Remote work

Job summary

IQVIA is seeking a country/region level Site Activation specialist for a home-based position. You will perform feasibility and site activation tasks in accordance with SOPs, regulatory requirements, and project guidelines, collaborating with the SAM and PM teams to ensure timely site startup.

The role requires fluency in Dutch and French to support sites in both languages and is based remotely, with responsibilities spanning regulatory and ethics documentation and data maintenance across

Qualifications

• Bachelor’s Degree Life science or related field required.
• 2 years’ experience in a clinical research environment.
• IQVIA is a leading global provider of clinical research services.

Responsibilities

• Perform feasibility, site activation and maintenance activities for investigative sites.
• Review documents for completeness and accuracy under guidance.
• Prepare and review site regulatory documents and informed consent forms.
• Support updating internal systems and project timelines with accurate data.

Education

Bachelor’s Degree Life science or related field

Job description

Job Overview

Under general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities.

Home Based opportunity requiring fluency in both Dutch and French in order to support sites in both languages.

Essential Function s

Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.

Review documents for completeness, consistency and accuracy, under guidance of senior staff.

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.

Support the updating and maintenance of 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.

Qualification s

Bachelor’s Degree Life science or related field Req

With 2 years’ experience in a clinical research environment.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.