Senior Site Activation Coordinator - IQVIA Biotech

IQVIA; Zaventem; On-site; EUR 45,000 - 75,000; Full time

Job summary

IQVIA LLC is seeking a country/region level site activation professional. This home-based role requires fluency in both Dutch and French to support sites in both languages.

You will assist feasibility, activation and maintenance activities in accordance with regulations, SOPs and project requirements. Ideal candidates hold a Life science degree with 2 years’ clinical research experience and will work under general supervision within a global team.

Qualifications

• Bachelor's Degree in Life science or related field.
• At least 2 years’ experience in a clinical research environment.

Responsibilities

• Assist with feasibility, site activation and maintenance activities for investigative sites.
• Review regulatory and ethics documents for completeness and accuracy.
• Prepare site documentation and distribute to sites and project teams.
• Support updating and maintaining internal systems and project plans with accurate information.

Skills

Site activation

Regulatory documentation

Education

Bachelor's degree Life science

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 Functions

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.

Qualifications

Bachelor's Degree Life science or related field. Req With 2 years’ experience in a clinical research environment.

Company Information

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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.