Senior Clinical Research Associate (CRA) I - Remote (Madrid)

Overview

The Senior Clinical Research Associate (CRA) I position is dedicated to conducting on-site and remote monitoring of clinical research studies, ensuring compliance with clinical practices, and supporting the successful execution of clinical trials.

In Short

• Conduct on-site and remote monitoring of clinical research studies.
• Ensure compliance with clinical practices and study protocols.
• Develop and implement quality monitoring tools and procedures.
• Collaborate with cross-functional teams for clinical trial activities.
• Provide training and mentorship to junior staff members.
• Manage and direct the work of lower-level professionals.
• Ensure accurate documentation and reporting of clinical trial data.
• Identify and resolve issues related to clinical trial conduct.
• Participate in the development of clinical trial protocols.
• Maintain detailed records of monitoring activities.

Requirements

• Bachelor's degree in a related field.
• 4-5 years of experience in clinical research.
• In-depth knowledge of clinical trial processes and regulations.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and in a team.
• Proficiency in clinical trial management systems.
• Strong organizational and time management skills.
• Knowledge of Good Clinical Practice (GCP) guidelines.
• Certification as a Clinical Research Professional preferred.

Benefits

• Opportunities for career development and progression.
• Supportive and engaged line management.
• Technical and therapeutic area training.
• Peer recognition and total rewards program.
• Inclusive culture that values diversity.
• Access to comprehensive resources and emerging technologies.
• Work in specialized teams aligned for expert collaboration.
• Impactful work improving patients' lives worldwide.
• Flexible working environment.
• Partnership with a diverse team of experts.