Clinical Research Associate II

This is a fully remote position, open to applicants in Spain.

📋 Description

• Oversee investigative sites throughout Spain

• Execute site qualification, initiation, monitoring, and close-out visits

• Guarantee patient safety, data accuracy, and adherence to protocols

• Conduct source data verification and assess study documentation

• Cultivate site relationships and offer continuous support to investigators and study personnel

• Aid in ethics committee and regulatory submissions as needed

• Supervise investigational product accountability and site performance

• Maintain Trial Master File (TMF) documentation and assist in query resolution

• Collaborate with cross-functional study teams to ensure effective trial execution

⛳️ Requirements

• Degree in Life Sciences or equivalent experience

• Certified CRA training

• At least 4 years of clinical research experience

• A minimum of 2 years of monitoring experience as a CRA

• Strong understanding of ICH-GCP, clinical trial regulations, and site management

• Proficient in Spanish and English

• Knowledge of Portuguese is a plus

• Exceptional communication, organizational, and problem-solving abilities

• Capacity to work independently and juggle multiple priorities

• Valid driver's license required

• Willingness to travel up to 75%

🏝️ Benefits

• Flexibility to work from home

• Chance to engage in international clinical trials

• Supportive and collaborative team environment

• Competitive salary along with a comprehensive benefits package