About Our Client
Our client is a leading global pharmaceutical company committed to advancing science and transforming patient outcomes. With a robust pipeline of innovative therapies, particularly in oncology, they are at the forefront of developing next-generation treatments. The Taiwan operations are integral to the global clinical development strategy, fostering a collaborative culture where expertise, agility, and passion for science drive meaningful impact. Employees are empowered to contribute to groundbreaking research while continuously developing their skills within a supportive and forward-thinking environment.
Job Description
- Independently manage and monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements.
- Experience in Cell Therapy (CAR-T) is a strong plus; experience in solid tumors is a must.
- Collaborate with cross-functional global teams to ensure trial objectives are met within timelines and quality standards.
- Identify and resolve site issues, ensuring data integrity and patient safety.
- Support study start-up, regulatory submissions, and site readiness activities.
- Mentor and support junior CRAs, fostering a culture of continuous learning and excellence.
The Successful Applicant
5+ years of work experience as (Sr) CRA within global CROs or pharmaceutical companies.Demonstrated expertise in solid tumor clinical trials; experience in CAR-T or Cell Therapy is highly desirable.Strong understanding of ICH-GCP, local regulatory requirements, and clinical development processes.Excellent communication, problem-solving, and organizational skills.Proven learning agility and adaptability in dynamic clinical environments.Team-oriented with a proactive, solution-focused approach.Fluency in English and Mandarin.