Cra Ii

Syneos Health · ESP-Madrid-Hybrid · hybrid Syneos Health is seeking a CRA II to join their Clinical Solutions team in Madrid or Barcelona. The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits, ensuring regulatory, ICH-GCP, and protocol compliance. Key responsibilities include: Evaluating site performance and providing recommendations for site-specific actions Verifying informed consent and protecting subject/patient confidentiality Assessing site processes and conducting source document reviews Applying query resolution techniques and providing guidance to site staff Managing investigational product inventory and verifying dispensing and administration Reviewing investigator site files and reconciling contents with trial master files Documenting activities and supporting subject/patient recruitment and retention Collaborating with study site personnel and central monitoring associates Preparing for and attending investigator meetings and sponsor face-to-face meetings Requirements: Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Excellent communication, presentation, and interpersonal skills Ability to manage required travel of up to 75% on a regular basis Syneos Health offers a range of benefits, including career development and progression, supportive line management, technical and therapeutic area training, and total rewards programs.