CRA2/SR CRA1- Sponsor dedicated- Lithuania

Clinical Research Associate

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 at least 1 year of on-site monitoring experience.

Very good computer skills including MS Office

Excellent command of Lithuanian 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

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

R1478548