Description
We are hiring CRAs and SCRAs in Central & Western Ukraine!
Join IQVIA and take the next step in your clinical research career. Be part of a global team and make a meaningful impact on patients’ outcomes.
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
- Experience monitoring clinical studies in the CVRM (Cardiovascular, Renal, and Metabolic) therapeutic area is preferred
- Very good computer skills including MS Office
- Excellent command of Ukrainian 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 stable, international, reputable company
- Company car or car allowance, mobile phone and attractive benefits package