CRA II

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.