Job Description
Join the forefront of pharmaceutical innovation at Novartis, a global leader in biopharmaceuticals. We seek a passionate Senior Clinical Research Associate to drive clinical trials that transform patient lives. Based in our Basel headquarters, you'll collaborate with cross-functional teams to ensure study protocols meet regulatory standards while advancing groundbreaking therapies.
This role offers competitive compensation, comprehensive benefits, and opportunities for professional growth in an inclusive, research-driven environment. Your work will directly impact the development of next-generation treatments for patients worldwide.
Responsibilities
- Design and implement clinical trial protocols ensuring compliance with GCP regulations
- Monitor investigational sites for protocol adherence and data integrity
- Lead vendor management relationships for CRO partnerships
- Conduct risk-based monitoring strategies for clinical trials
- Collaborate with medical teams to review adverse events and safety reports
- Prepare regulatory documentation and study submissions
- Mentor junior CRAs and contribute to process optimization
Qualifications
- Master's degree in Life Sciences, Pharmacy, or related field
- 5+ years of clinical research experience in pharmaceuticals
- Certified Clinical Research Associate (CCRA) or equivalent certification
- Expertise in ICH-GCP and global regulatory requirements
- Strong proficiency in clinical trial management systems (e.g., Veeva Vault RIM)
- Proven track record in managing Phase II-III trials
- Exceptional communication and stakeholder management skills
- Fluency in English and German