CRA II

CRA II – Bucharest, Romania (Hybrid)

We are seeking Clinical Research Associates at CRA II level to join a growing clinical research team within a global biopharmaceutical company (FSP model).

The Role

As a CRA II, you will be responsible for clinical trial monitoring, ensuring protocol compliance, patient safety, data integrity and ICH-GCP standards.

Requirements

• University degree in a relevant field such as life sciences, nursing or medicine.
• 12 months of experience in independent on-site monitoring of clinical trials (experience in SSVs, SIVs, IMVs , COVs)
• The role requires attendance in the office 1–2 days per week
• Strong understanding of clinical trial processes and local regulatory requirements
• Willingness to travel 65% of the time
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

Experience in Cardiology, Haematology/Oncology, Inflammation, Metabolic Disorders, Neurology or Rare Diseases is advantageous but not essential.

What We Offer

• Hybrid working in Bucharest
• Structured one-month onboarding programme covering systems, processes, study requirements and monitoring procedures.
• Ongoing support and development.
• Competitive salary and performance related incentives.
• Opportunity to work across a range of clinical studies and therapeutic areas.