Clinical Research Associate

About the role

TFS HealthScience, a global mid‑size CRO, is seeking a Clinical Research Associate to join its SRS/FSP team. You will be dedicated to a leading global pharmaceutical sponsor, overseeing site activities throughout the clinical trial lifecycle to ensure patient safety, data integrity, and regulatory compliance.

Key responsibilities

• Conduct Site Selection, Initiation, Interim Monitoring, and Close‑Out visits.
• Verify that investigator sites adhere to the study protocol, ICH‑GCP, sponsor requirements, and local regulations.
• Monitor patient safety, data quality, and study documentation from start‑up to study close‑out.
• Develop and maintain strong relationships with investigators, site staff, and sponsor stakeholders.
• Support site readiness, subject recruitment, and issue resolution to keep study timelines on track.
• Identify, document, and escalate risks while applying risk‑based monitoring approaches.
• Assist with audit and inspection readiness activities as needed.

Required profile

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum 3 years of independent clinical monitoring experience in pharma, biotech, or CRO environments.
• Strong knowledge of ICH‑GCP guidelines and applicable regulatory requirements.
• Proven experience managing sites from initiation through close‑out.
• Excellent communication and relationship‑building abilities.
• Fluent written and spoken English.
• Willingness to travel regularly within the assigned country and a valid driving licence.

Required skills

What we offer

• Opportunities for personal and professional growth in a collaborative environment.
• Competitive salary aligned with local market conditions, plus applicable benefits.
• A culture guided by Trust, Quality, Passion, Flexibility, and Sustainability.