Clinical Research Associate II

Psicro; Madrid; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

Stability and long-term cooperation

Permanent contract

Competitive salary and benefits

Job summary

Psicro is seeking a Clinical Research Associate II to oversee on-site monitoring across Phase II/III trials in Spain, liaising with study sites and investigators to ensure patient safety and data quality.

You will conduct SIV, RMV, COV visits, manage site communications, support regulatory submissions, and collaborate with internal teams. Requires Life Sciences degree, Master’s in Clinical Trials, English/Spanish, and willingness to travel.

Qualifications

• A degree in Life Sciences and a Master’s degree in Clinical Trials are required.
• Full working proficiency in English and Spanish is required.
• Ability to plan, multitask and work in a dynamic team environment.

Responsibilities

• Conduct and report SIV, RMV, COV onsite monitoring visits.
• Perform CRF review, source document verification and query resolution.
• Site communication and management responsibilities.
• Point of contact for in-house support services and vendors.
• Communicate with internal project teams regarding study progress.
• Participate in feasibility research and regulatory support for study submissions.
• Prepare and participate in audits and inspections.

Skills

English proficiency

Spanish proficiency

MS Office

Communication

Teamwork

Travel flexibility

Education

Life Sciences degree

Master’s in Clinical Trials

Tools

MS Office

Job description

As a Clinical Research Associate 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

Requirements:

• A degree in Life Sciences and a Master's 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 and Spanish
• Proficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

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.