CRA II

The Company:
Our client is a Top-Tier Global Clinical Research Organization (CRO) and a premier leader in healthcare intelligence. Operating across 40+ countries, they provide end-to-end drug development solutions for the world’s leading biopharmaceutical companies. This role sits within their specialized high-growth division, focusing on cutting-edge clinical trials that are shaping the future of medicine.

The Role:

CRA I/CRA II

Key Responsibilities
Site Management:
Conduct the full range of site visits, including qualification, initiation, routine monitoring, and close-out.
Compliance & Safety:
Ensure strict protocol adherence and data integrity while upholding patient safety in accordance with ICH-GCP guidelines and local regulations.
Stakeholder

Collaboration:

Build and maintain strong relationships with investigators and site staff to facilitate smooth study conduct and resolve site-level issues.
Data Quality:
Perform rigorous data reviews and resolution of queries to maintain the highest quality of clinical data for study reporting.
Documentation:
Contribute to the preparation and review of essential study documents, including clinical study reports and site monitoring logs.

Your Profile:

Education:

Bachelor’s degree in a scientific, healthcare, or related life sciences field.

Experience:

A minimum of 3 years of hands-on experience as a Clinical Research Associate with a strong background in On-Site Monitoring. (Global Studies not local)
Therapeutic Expertise:
Mandatory experience in Oncology or Immunology therapeutic areas.
Regulatory Knowledge:
In-depth understanding of clinical trial processes, global regulations, and ICH-GCP guidelines.
Technical

Skills:

Proficient in using Clinical Trial Management Systems (CTMS) and electronic Data Capture (eDC) platforms.

Soft Skills:

Exceptional organizational and communication skills, with a sharp eye for detail and the ability to thrive in a fast-paced environment.