IQVIA is hiring CRAs / SCRAs
Join IQVIA today and make an impact on patients’ outcome!
Your responsibilities will include:
Performing site selection, initiation, monitoring and close-out visits
Supporting the development of a subject recruitment plan
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
Collaborating with experts at study sites and with client representatives
Qualifications:
University degree in scientific discipline or health care
Requires 2-3 year of on-site monitoring experience.
Very good computer skills including MS Office
Excellent command of Ukranian and English language.
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility to travel
Driver’s license class B
What you can expect:
Resources that promote your career growth
Leaders that support flexible work schedules
Programs to help you build your therapeutic knowledge
Excellent working environment in a stabile, international, reputable company
Company car or car allowance, mobile phone and attractive benefits package
#weareIQVIA #projectpatientfocus #LI-Remote #CRASDAJD #CRA #fspcares
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