Bachelor's Degree in Life Science or related field
Minimum 2 years' work experience; 1+ years in healthcare or similar
Good interpersonal, communication, and organisational skills to establish and maintain effective working relationships with co-workers, managers, and sponsors
Ability to work on multiple projects
Exposure across 21 Therapeutic Areas
Be part of a global team that operates across 141 locations
Exposure across a variety of studies and projects
Access to new, innovative technologies
Work within a collaborative and vibrant environment
Own your career
Senior Site Activation Coordinator, Nordic Speaking - Bloemfontein - IQVIA Argentina
Description
Senior Site Activation Coordinator
Languages: Nordics & English
Based in Serbia/Bulgaria/Ukraine/South Africa/Croatia/Türkiye
Make an impact on patient health
IQVIA's Global Site Activation Team of 2000 employees drives best in class site and customer experience, with industry leading outcomes.
We keep the patient at the forefront; 'Always Impatient for the Patient' and we excel in our collaboration with our external/internal customers.
IQVIA's Country Site Activation team is a global network that identifies and activates sites to the highest quality to ensure patients on clinical trials have access to safe and effective medication.
We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.
Job Overview:
As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities.
These activities will be in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines.
You will 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, Project Management team, and other departments as necessary.
Coupled with reviewing documents for completeness, consistency, and accuracy, under the guidance of senior staff, you will prepare site documents, review, track, and follow up on the progress, approval, and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.
You will also support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
Requirements:
Join us and let's create a healthier world together:
Unleash your potential
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
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.