CRA/Sr CRA -Sponsor dedicated-Bulgaria

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.

Requirements

• 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

Benefits

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Better Work-Life balance, optimal DOS
• Company car or car allowance, mobile phone and attractive benefits package