Clinical Research Associate, Sponsor-dedicated - Croatia
- Zagreb
- Stalni radni odnos
- Puno radno vrijeme
- 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 (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
- University degree in scientific discipline or health care
- At least 1 year of on-site monitoring experience
- Good knowledge of clinical research regulatory requirements
- Very good computer skills including MS Office
- Excellent command of Croatian 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