Senior Clinical Research Associate

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

📋 Description

• Oversee and take responsibility for the advancement of clinical studies at investigative sites.

• Ensure that studies are executed, documented, and reported in alignment with the protocol, SOPs, ICH-GCP, and relevant regulations and standards.

• Coordinate activities related to study setup and monitoring, including identifying investigators, managing regulatory submissions, and conducting pre-study and initiation visits.

• Manage clinical trials of appropriate scale.

• Provide support to larger clinical study teams.

• Train and guide junior staff members.

• Engage directly with clients.

• Initiate payments.

• Take part in proposal activities, which include development and client presentations.

⛳️ Requirements

• Bachelor's degree or equivalent experience.

• Possession of a CRA certification.

• At least 5 years of CRA/SCRA experience in a CRO, pharmaceutical, biotechnology, or medical device setting.

• Significant experience in IVD (In Vitro Diagnostics), oncology, infectious diseases, and gastrointestinal studies.

• Demonstrated experience in monitoring studies across various European countries.

• Willingness to travel domestically, including overnight stays, with a travel commitment of approximately 50–60%.

• International travel may be necessary for certain senior-level roles.

• Proficiency in both Spanish and English is mandatory.

• Applications should be submitted in English.

🏝️ Benefits

• Employees are empowered to make a significant impact.

• Establish meaningful relationships with clients.

• Opportunities for career advancement.

• Access to professional development resources.

• Work in a collaborative and quality-driven environment.

• Equal opportunity employer.

• Reasonable accommodations are available during the application process.