We are seeking an experienced Clinical Research Associate, fully sponsor-dedicated, with a strong background in oncology trials. This is an excellent opportunity to advance your career within a leading global CRO, where you’ll work in a stable, supportive, and international environment that values quality and professional growth.

Your responsibilities will include:

Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representatives

Qualifications:

University degree in scientific discipline or health care1+ years of on-site monitoring experienceGood knowledge of clinical research regulatory requirementsVery good computer skills including MS OfficeExcellent command of Bulgarian and English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver’s license class B

What you can expect:

Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeBetter Work-Life balance, optimal DOSCompany car or car allowance, mobile phone and attractive benefits package

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