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.

As 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/budgetary guidelines. Your task may also include maintenance activities.

Perform site activation 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 staffPrepare site regulatory documents, reviewing for completeness and accuracyReview, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documentsDistribute completed documents to sites and internal project team membersSupport the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Bachelor’s Degree in Life Science or related field experience preferredMinimum 1 years’ work experience; 1+ years in healthcare or similar considered advantageousFluent/ native language capabilities, including EnglishProductive individual contributor who works well under general supervisionGood interpersonal communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsorsAbility to handle change and ambiguityApplicants will benefit from having a general awareness of the clinical trial environment and drug development process as well as working on multiple projectsGood technology skills and knowledge of MS Office applications

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

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.https://jobs.iqvia.com/covid-19-vaccine-status

The potential base pay range for this role, when annualized, is $42,400.00 - $70,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.