Country Site Activation Internship - 6 months

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 are a global network who identify and activate 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
Under supervision, executes the site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at country level.

Job Responsbilities

• With supervision, serve a Single Point of Contact (SPOC) to perform 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.

• Update and maintain 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 sciences or a related field. Desirable specific training in clinical research or CRA school.

• Desirable 1 - 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.