Clinical Research Associate II

As a CRA II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  Your focus will be on subjects rights safety and well-being and quality of data compliance.

You will:

• Conduct and report SIV RMV COV onsite monitoring visits
• Perform CRF review source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions
• Prepare and participate on audits and inspections

Qualifications :

• A degree in Life Sciences and a Masters degree in Clinical Trials are required
• At least 1 year of independent on-site monitoring experience in Spain
• Experience in all types of monitoring visits in Phase II and/or III
• Full working proficiency in English Spanish and Catalan
• Proficiency in MS Office applications
• Ability to plan multitask and work in a dynamic team environment
• Communication collaboration and problem-solving skills
• Ability to travel

Additional Information :

What We Offer:

• Stability long-term cooperation
• Permanent contract full-time job
• Competitive salary and benefit package
• Career development 
• Unique combination of team collaboration and independent work
• Friendly and supportive colleagues
• Onboarding courses about clinical research industry
• Comfortable and well-established office

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success. 

Remote Work :

No

Employment Type :

Full-time